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Erschienen in: Cancer and Metastasis Reviews 3/2008

01.09.2008

Clinical biomarkers of angiogenesis inhibition

verfasst von: Aaron P. Brown, Deborah E. Citrin, Kevin A. Camphausen

Erschienen in: Cancer and Metastasis Reviews | Ausgabe 3/2008

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Abstract

Introduction

An expanding understanding of the importance of angiogenesis in oncology and the development of numerous angiogenesis inhibitors are driving the search for biomarkers of angiogenesis. We review currently available candidate biomarkers and surrogate markers of anti-angiogenic agent effect.

Discussion

A number of invasive, minimally invasive, and non-invasive tools are described with their potential benefits and limitations. Diverse markers can evaluate tumor tissue or biological fluids, or specialized imaging modalities.

Conclusions

The inclusion of these markers into clinical trials may provide insight into appropriate dosing for desired biological effects, appropriate timing of additional therapy, prediction of individual response to an agent, insight into the interaction of chemotherapy and radiation following exposure to these agents, and perhaps most importantly, a better understanding of the complex nature of angiogenesis in human tumors. While many markers have potential for clinical use, it is not yet clear which marker or combination of markers will prove most useful.
Literatur
1.
Zurück zum Zitat Folkman, J. (1971). Tumor angiogenesis: Therapeutic implications. The New England Journal of Medicine, 285(21), 1182–1186.PubMed Folkman, J. (1971). Tumor angiogenesis: Therapeutic implications. The New England Journal of Medicine, 285(21), 1182–1186.PubMed
2.
Zurück zum Zitat Carmeliet, P. (2005). Angiogenesis in life, disease and medicine. Nature, 438(7070), 932–936.PubMed Carmeliet, P. (2005). Angiogenesis in life, disease and medicine. Nature, 438(7070), 932–936.PubMed
3.
Zurück zum Zitat Carmeliet, P., & Jain, R. K. (2000). Angiogenesis in cancer and other diseases. Nature, 407(6801), 249–257.PubMed Carmeliet, P., & Jain, R. K. (2000). Angiogenesis in cancer and other diseases. Nature, 407(6801), 249–257.PubMed
4.
Zurück zum Zitat Ferrara, N., & Kerbel, R. S. (2005). Angiogenesis as a therapeutic target. Nature, 438(7070), 967–974.PubMed Ferrara, N., & Kerbel, R. S. (2005). Angiogenesis as a therapeutic target. Nature, 438(7070), 967–974.PubMed
5.
Zurück zum Zitat Nieder, C., et al. (2006). Current status of angiogenesis inhibitors combined with radiation therapy. Cancer Treatment Reviews, 32(5), 348–364.PubMed Nieder, C., et al. (2006). Current status of angiogenesis inhibitors combined with radiation therapy. Cancer Treatment Reviews, 32(5), 348–364.PubMed
6.
Zurück zum Zitat Quesada, A. R., Munoz-Chapuli, R., & Medina, M. A. (2006). Anti-angiogenic drugs: From bench to clinical trials. Medicinal Research Reviews, 26(4), 483–530.PubMed Quesada, A. R., Munoz-Chapuli, R., & Medina, M. A. (2006). Anti-angiogenic drugs: From bench to clinical trials. Medicinal Research Reviews, 26(4), 483–530.PubMed
7.
Zurück zum Zitat Walsh, D. A. (2007). Pathophysiological mechanisms of angiogenesis. Advances in Clinical Chemistry, 44, 187–221.PubMed Walsh, D. A. (2007). Pathophysiological mechanisms of angiogenesis. Advances in Clinical Chemistry, 44, 187–221.PubMed
8.
Zurück zum Zitat Ferrara, N. (2004). Vascular endothelial growth factor: Basic science and clinical progress. Endocrine Reviews, 25(4), 581–611.PubMed Ferrara, N. (2004). Vascular endothelial growth factor: Basic science and clinical progress. Endocrine Reviews, 25(4), 581–611.PubMed
9.
Zurück zum Zitat Longo, R., & Gasparini, G. (2007). Challenges for patient selection with VEGF inhibitors. Cancer Chemotherapy and Pharmacology, 60(2), 151–170.PubMed Longo, R., & Gasparini, G. (2007). Challenges for patient selection with VEGF inhibitors. Cancer Chemotherapy and Pharmacology, 60(2), 151–170.PubMed
10.
Zurück zum Zitat Moreira, I. S., Fernandes, P. A., & Ramos, M. J. (2007). Vascular endothelial growth factor (VEGF) inhibition—A critical review. Anti-Cancer Agents in Medicinal Chemistry, 7(2), 223–245.PubMed Moreira, I. S., Fernandes, P. A., & Ramos, M. J. (2007). Vascular endothelial growth factor (VEGF) inhibition—A critical review. Anti-Cancer Agents in Medicinal Chemistry, 7(2), 223–245.PubMed
11.
Zurück zum Zitat Arora, N., et al. (1999). Vascular endothelial growth factor chimeric toxin is highly active against endothelial cells. Cancer Research, 59(1), 183–188.PubMed Arora, N., et al. (1999). Vascular endothelial growth factor chimeric toxin is highly active against endothelial cells. Cancer Research, 59(1), 183–188.PubMed
12.
Zurück zum Zitat Frankel, A. E. (2002). Increased sophistication of immunotoxins. Clinical Cancer Research, 8(4), 942–944.PubMed Frankel, A. E. (2002). Increased sophistication of immunotoxins. Clinical Cancer Research, 8(4), 942–944.PubMed
13.
Zurück zum Zitat Hicklin, D. J., & Ellis, L. M. (2005). Role of the vascular endothelial growth factor pathway in tumor growth and angiogenesis. Journal of Clinical Oncology, 23(5), 1011–1027.PubMed Hicklin, D. J., & Ellis, L. M. (2005). Role of the vascular endothelial growth factor pathway in tumor growth and angiogenesis. Journal of Clinical Oncology, 23(5), 1011–1027.PubMed
14.
Zurück zum Zitat Yang, J. C., et al. (2003). A randomized trial of bevacizumab, an anti-vascular endothelial growth factor antibody, for metastatic renal cancer. The New England Journal of Medicine, 349(5), 427–434.PubMed Yang, J. C., et al. (2003). A randomized trial of bevacizumab, an anti-vascular endothelial growth factor antibody, for metastatic renal cancer. The New England Journal of Medicine, 349(5), 427–434.PubMed
15.
Zurück zum Zitat Moffat, B. A., et al. (2006). Inhibition of vascular endothelial growth factor (VEGF)-A causes a paradoxical increase in tumor blood flow and up-regulation of VEGF-D. Clinical Cancer Research, 12(5), 1525–1532.PubMed Moffat, B. A., et al. (2006). Inhibition of vascular endothelial growth factor (VEGF)-A causes a paradoxical increase in tumor blood flow and up-regulation of VEGF-D. Clinical Cancer Research, 12(5), 1525–1532.PubMed
16.
Zurück zum Zitat Senan, S., & Smit, E. F. (2007). Design of clinical trials of radiation combined with antiangiogenic therapy. Oncologist, 12(4), 465–477.PubMed Senan, S., & Smit, E. F. (2007). Design of clinical trials of radiation combined with antiangiogenic therapy. Oncologist, 12(4), 465–477.PubMed
17.
Zurück zum Zitat Folkman, J., & Camphausen, K. (2001). CANCER: Enhanced: What does radiotherapy do to endothelial cells? Science, 293(5528), 227–228.PubMed Folkman, J., & Camphausen, K. (2001). CANCER: Enhanced: What does radiotherapy do to endothelial cells? Science, 293(5528), 227–228.PubMed
18.
Zurück zum Zitat Wachsberger, P., Burd, R., & Dicker, A. P. (2003). Tumor response to ionizing radiation combined with antiangiogenesis or vascular targeting agents: Exploring mechanisms of interaction. Clinical Cancer Research, 9(6), 1957–1971.PubMed Wachsberger, P., Burd, R., & Dicker, A. P. (2003). Tumor response to ionizing radiation combined with antiangiogenesis or vascular targeting agents: Exploring mechanisms of interaction. Clinical Cancer Research, 9(6), 1957–1971.PubMed
19.
Zurück zum Zitat Brizel, D. M., et al. (1999). Oxygenation of head and neck cancer: Changes during radiotherapy and impact on treatment outcome. Radiotherapy and Oncology, 53(2), 113–117.PubMed Brizel, D. M., et al. (1999). Oxygenation of head and neck cancer: Changes during radiotherapy and impact on treatment outcome. Radiotherapy and Oncology, 53(2), 113–117.PubMed
20.
Zurück zum Zitat Brizel, D. M., et al. (1996). Tumor oxygenation predicts for the likelihood of distant metastases in human soft tissue sarcoma. Cancer Research, 56(5), 941–943.PubMed Brizel, D. M., et al. (1996). Tumor oxygenation predicts for the likelihood of distant metastases in human soft tissue sarcoma. Cancer Research, 56(5), 941–943.PubMed
21.
Zurück zum Zitat Hall, E. (2000). Radiobiology for the radiologist (5th ed.). Philadelphia: Lippincott, Williams, & Wilkins. Hall, E. (2000). Radiobiology for the radiologist (5th ed.). Philadelphia: Lippincott, Williams, & Wilkins.
22.
Zurück zum Zitat Dewhirst, M. W., et al. (2007). Exploring the role of HIF-1 in early angiogenesis and response to radiotherapy. Radiotherapy and Oncology, 83(3), 249–255.PubMed Dewhirst, M. W., et al. (2007). Exploring the role of HIF-1 in early angiogenesis and response to radiotherapy. Radiotherapy and Oncology, 83(3), 249–255.PubMed
23.
Zurück zum Zitat Moeller, B. J., et al. (2004). Radiation activates HIF-1 to regulate vascular radiosensitivity in tumors: Role of reoxygenation, free radicals, and stress granules. Cancer Cell, 5(5), 429–441.PubMed Moeller, B. J., et al. (2004). Radiation activates HIF-1 to regulate vascular radiosensitivity in tumors: Role of reoxygenation, free radicals, and stress granules. Cancer Cell, 5(5), 429–441.PubMed
24.
Zurück zum Zitat Harada, H., et al. (2007). Significance of HIF-1-active cells in angiogenesis and radioresistance. Oncogene, 26, 7508–7516.PubMed Harada, H., et al. (2007). Significance of HIF-1-active cells in angiogenesis and radioresistance. Oncogene, 26, 7508–7516.PubMed
25.
Zurück zum Zitat Gaffney, D. K., et al. (2003). Epidermal growth factor receptor (EGFR) and vascular endothelial growth factor (VEGF) negatively affect overall survival in carcinoma of the cervix treated with radiotherapy. International Journal of Radiation Oncology, Biology, Physics, 56(4), 922–928.PubMed Gaffney, D. K., et al. (2003). Epidermal growth factor receptor (EGFR) and vascular endothelial growth factor (VEGF) negatively affect overall survival in carcinoma of the cervix treated with radiotherapy. International Journal of Radiation Oncology, Biology, Physics, 56(4), 922–928.PubMed
26.
Zurück zum Zitat Gorski, D. H., et al. (1999). Blockage of the vascular endothelial growth factor stress response increases the antitumor effects of ionizing radiation. Cancer Research, 59(14), 3374–3378.PubMed Gorski, D. H., et al. (1999). Blockage of the vascular endothelial growth factor stress response increases the antitumor effects of ionizing radiation. Cancer Research, 59(14), 3374–3378.PubMed
27.
Zurück zum Zitat Kermani, P., et al. (2001). Effect of ionizing radiation on thymidine uptake, differentiation, and VEGFR2 receptor expression in endothelial cells: The role of VEGF(165). International Journal of Radiation Oncology, Biology, Physics, 50(1), 213–220.PubMed Kermani, P., et al. (2001). Effect of ionizing radiation on thymidine uptake, differentiation, and VEGFR2 receptor expression in endothelial cells: The role of VEGF(165). International Journal of Radiation Oncology, Biology, Physics, 50(1), 213–220.PubMed
28.
Zurück zum Zitat Sonveaux, P., et al. (2003). Irradiation-induced angiogenesis through the up-regulation of the nitric oxide pathway: Implications for tumor radiotherapy. Cancer Research, 63(5), 1012–1019.PubMed Sonveaux, P., et al. (2003). Irradiation-induced angiogenesis through the up-regulation of the nitric oxide pathway: Implications for tumor radiotherapy. Cancer Research, 63(5), 1012–1019.PubMed
29.
Zurück zum Zitat Teicher, B. A., Sotomayor, E. A., & Huang, Z. D. (1992). Antiangiogenic agents potentiate cytotoxic cancer therapies against primary and metastatic disease. Cancer Research, 52(23), 6702–6704.PubMed Teicher, B. A., Sotomayor, E. A., & Huang, Z. D. (1992). Antiangiogenic agents potentiate cytotoxic cancer therapies against primary and metastatic disease. Cancer Research, 52(23), 6702–6704.PubMed
30.
Zurück zum Zitat Batchelor, T. T., et al. (2007). AZD2171, a pan-VEGF receptor tyrosine kinase inhibitor, normalizes tumor vasculature and alleviates edema in glioblastoma patients. Cancer Cell, 11(1), 83–95.PubMed Batchelor, T. T., et al. (2007). AZD2171, a pan-VEGF receptor tyrosine kinase inhibitor, normalizes tumor vasculature and alleviates edema in glioblastoma patients. Cancer Cell, 11(1), 83–95.PubMed
31.
Zurück zum Zitat Dings, R. P., et al. (2007). Scheduling of radiation with angiogenesis inhibitors anginex and Avastin improves therapeutic outcome via vessel normalization. Clinical Cancer Research, 13(11), 3395–3402.PubMed Dings, R. P., et al. (2007). Scheduling of radiation with angiogenesis inhibitors anginex and Avastin improves therapeutic outcome via vessel normalization. Clinical Cancer Research, 13(11), 3395–3402.PubMed
32.
Zurück zum Zitat Fukumura, D., & Jain, R. K. (2007). Tumor microenvironment abnormalities: Causes, consequences, and strategies to normalize. Journal of Cellular Biochemistry, 101(4), 937–949.PubMed Fukumura, D., & Jain, R. K. (2007). Tumor microenvironment abnormalities: Causes, consequences, and strategies to normalize. Journal of Cellular Biochemistry, 101(4), 937–949.PubMed
33.
Zurück zum Zitat Fukumura, D., & Jain, R. K. (2007). Tumor microvasculature and microenvironment: Targets for anti-angiogenesis and normalization. Microvascular Research, 74, 72–84.PubMed Fukumura, D., & Jain, R. K. (2007). Tumor microvasculature and microenvironment: Targets for anti-angiogenesis and normalization. Microvascular Research, 74, 72–84.PubMed
34.
Zurück zum Zitat Winkler, F., et al. (2004). Kinetics of vascular normalization by VEGFR2 blockade governs brain tumor response to radiation: Role of oxygenation, angiopoietin-1, and matrix metalloproteinases. Cancer Cell, 6(6), 553–563.PubMed Winkler, F., et al. (2004). Kinetics of vascular normalization by VEGFR2 blockade governs brain tumor response to radiation: Role of oxygenation, angiopoietin-1, and matrix metalloproteinases. Cancer Cell, 6(6), 553–563.PubMed
35.
Zurück zum Zitat Riesterer, O., et al. (2006). Ionizing radiation antagonizes tumor hypoxia induced by antiangiogenic treatment. Clinical Cancer Research, 12(11 Pt 1), 3518–3524.PubMed Riesterer, O., et al. (2006). Ionizing radiation antagonizes tumor hypoxia induced by antiangiogenic treatment. Clinical Cancer Research, 12(11 Pt 1), 3518–3524.PubMed
36.
Zurück zum Zitat Kummar, S., et al. (2007). Compressing drug development timelines in oncology using phase ‘0’ trials. Nature Reviews. Cancer, 7(2), 131–139.PubMed Kummar, S., et al. (2007). Compressing drug development timelines in oncology using phase ‘0’ trials. Nature Reviews. Cancer, 7(2), 131–139.PubMed
37.
Zurück zum Zitat Citrin, D., Menard, C., & Camphausen, K. (2006). Combining radiotherapy and angiogenesis inhibitors: Clinical trial design. International Journal of Radiation Oncology, Biology, Physics, 64(1), 15–25.PubMed Citrin, D., Menard, C., & Camphausen, K. (2006). Combining radiotherapy and angiogenesis inhibitors: Clinical trial design. International Journal of Radiation Oncology, Biology, Physics, 64(1), 15–25.PubMed
38.
Zurück zum Zitat Jubb, A. M., et al. (2006). Predicting benefit from anti-angiogenic agents in malignancy. Nature Reviews. Cancer, 6(8), 626–635.PubMed Jubb, A. M., et al. (2006). Predicting benefit from anti-angiogenic agents in malignancy. Nature Reviews. Cancer, 6(8), 626–635.PubMed
39.
Zurück zum Zitat Korn, E. L., et al. (2001). Clinical trial designs for cytostatic agents: Are new approaches needed? Journal of Clinical Oncology, 19(1), 265–272.PubMed Korn, E. L., et al. (2001). Clinical trial designs for cytostatic agents: Are new approaches needed? Journal of Clinical Oncology, 19(1), 265–272.PubMed
40.
Zurück zum Zitat Bernsen, H. J., et al. (1995). Vascularity and perfusion of human gliomas xenografted in the athymic nude mouse. British Journal of Cancer, 71(4), 721–726.PubMed Bernsen, H. J., et al. (1995). Vascularity and perfusion of human gliomas xenografted in the athymic nude mouse. British Journal of Cancer, 71(4), 721–726.PubMed
41.
Zurück zum Zitat Bussink, J., Kaanders, J. H., & van der Kogel, A. J. (2003). Tumor hypoxia at the micro-regional level: Clinical relevance and predictive value of exogenous and endogenous hypoxic cell markers. Radiotherapy and Oncology, 67(1), 3–15.PubMed Bussink, J., Kaanders, J. H., & van der Kogel, A. J. (2003). Tumor hypoxia at the micro-regional level: Clinical relevance and predictive value of exogenous and endogenous hypoxic cell markers. Radiotherapy and Oncology, 67(1), 3–15.PubMed
42.
Zurück zum Zitat Macchiarini, P., et al. (1992). Relation of neovascularisation to metastasis of non-small-cell lung cancer. Lancet, 340(8812), 145–146.PubMed Macchiarini, P., et al. (1992). Relation of neovascularisation to metastasis of non-small-cell lung cancer. Lancet, 340(8812), 145–146.PubMed
43.
Zurück zum Zitat Weidner, N., et al. (1991). Tumor angiogenesis and metastasis-correlation in invasive breast carcinoma. The New England Journal of Medicine, 324(1), 1–8.PubMed Weidner, N., et al. (1991). Tumor angiogenesis and metastasis-correlation in invasive breast carcinoma. The New England Journal of Medicine, 324(1), 1–8.PubMed
44.
Zurück zum Zitat Zhong, H., et al. (1999). Overexpression of hypoxia-inducible factor 1alpha in common human cancers and their metastases. Cancer Research, 59(22), 5830–5835.PubMed Zhong, H., et al. (1999). Overexpression of hypoxia-inducible factor 1alpha in common human cancers and their metastases. Cancer Research, 59(22), 5830–5835.PubMed
45.
Zurück zum Zitat Agulnik, M., et al. (2006). Impact and perceptions of mandatory tumor biopsies for correlative studies in clinical trials of novel anticancer agents. Journal of Clinical Oncology, 24(30), 4801–4807.PubMed Agulnik, M., et al. (2006). Impact and perceptions of mandatory tumor biopsies for correlative studies in clinical trials of novel anticancer agents. Journal of Clinical Oncology, 24(30), 4801–4807.PubMed
46.
Zurück zum Zitat Helft, P. R., & Daugherty, C. K. (2006). Are we taking without giving in return? The ethics of research-related biopsies and the benefits of clinical trial participation. Journal of Clinical Oncology, 24(30), 4793–4795.PubMed Helft, P. R., & Daugherty, C. K. (2006). Are we taking without giving in return? The ethics of research-related biopsies and the benefits of clinical trial participation. Journal of Clinical Oncology, 24(30), 4793–4795.PubMed
47.
Zurück zum Zitat Willett, C. G., et al. (2004). Direct evidence that the VEGF-specific antibody bevacizumab has antivascular effects in human rectal cancer. Nature Medicine, 10(2), 145–147.PubMed Willett, C. G., et al. (2004). Direct evidence that the VEGF-specific antibody bevacizumab has antivascular effects in human rectal cancer. Nature Medicine, 10(2), 145–147.PubMed
48.
Zurück zum Zitat Willett, C. G., et al. (2005). Surrogate markers for antiangiogenic therapy and dose-limiting toxicities for bevacizumab with radiation and chemotherapy: Continued experience of a Phase I trial in rectal cancer patients. Journal of Clinical Oncology, 23(31), 8136–8139.PubMed Willett, C. G., et al. (2005). Surrogate markers for antiangiogenic therapy and dose-limiting toxicities for bevacizumab with radiation and chemotherapy: Continued experience of a Phase I trial in rectal cancer patients. Journal of Clinical Oncology, 23(31), 8136–8139.PubMed
49.
Zurück zum Zitat Kolev, Y., et al. Prognostic significance of VEGF expression in correlation with COX-2, microvessel density, and clinicopathological characteristics in human gastric carcinoma. Annals of Surgical Oncology, 14, 2738–2747. Kolev, Y., et al. Prognostic significance of VEGF expression in correlation with COX-2, microvessel density, and clinicopathological characteristics in human gastric carcinoma. Annals of Surgical Oncology, 14, 2738–2747.
50.
Zurück zum Zitat Lentsch, E. J., et al. (2006). Microvessel density in head and neck squamous cell carcinoma primary tumors and its correlation with clinical staging parameters. Laryngoscope, 116(3), 397–400.PubMed Lentsch, E. J., et al. (2006). Microvessel density in head and neck squamous cell carcinoma primary tumors and its correlation with clinical staging parameters. Laryngoscope, 116(3), 397–400.PubMed
51.
Zurück zum Zitat Nieto, Y., et al. (2007). Prognostic analysis of tumour angiogenesis, determined by microvessel density and expression of vascular endothelial growth factor, in high-risk primary breast cancer patients treated with high-dose chemotherapy. British Journal of Cancer, 97(3), 391–397.PubMed Nieto, Y., et al. (2007). Prognostic analysis of tumour angiogenesis, determined by microvessel density and expression of vascular endothelial growth factor, in high-risk primary breast cancer patients treated with high-dose chemotherapy. British Journal of Cancer, 97(3), 391–397.PubMed
52.
Zurück zum Zitat Uzzan, B., et al. (2004). Microvessel density as a prognostic factor in women with breast cancer: a systematic review of the literature and meta-analysis. Cancer Research, 64(9), 2941–2955.PubMed Uzzan, B., et al. (2004). Microvessel density as a prognostic factor in women with breast cancer: a systematic review of the literature and meta-analysis. Cancer Research, 64(9), 2941–2955.PubMed
53.
Zurück zum Zitat Hlatky, L., Hahnfeldt, P., & Folkman, J. (2002). Clinical application of antiangiogenic therapy: microvessel density, what it does and doesn’t tell us. Journal of the National Cancer Institute, 94(12), 883–893.PubMed Hlatky, L., Hahnfeldt, P., & Folkman, J. (2002). Clinical application of antiangiogenic therapy: microvessel density, what it does and doesn’t tell us. Journal of the National Cancer Institute, 94(12), 883–893.PubMed
54.
Zurück zum Zitat Tozer, G. M. (2003). Measuring tumour vascular response to antivascular and antiangiogenic drugs. British Journal of Radiology, 76(suppl_1), S23–S35.PubMed Tozer, G. M. (2003). Measuring tumour vascular response to antivascular and antiangiogenic drugs. British Journal of Radiology, 76(suppl_1), S23–S35.PubMed
55.
Zurück zum Zitat Beecken, W. D., et al. (2001). Effect of antiangiogenic therapy on slowly growing, poorly vascularized tumors in mice. Journal of the National Cancer Institute, 93(5), 382–387.PubMed Beecken, W. D., et al. (2001). Effect of antiangiogenic therapy on slowly growing, poorly vascularized tumors in mice. Journal of the National Cancer Institute, 93(5), 382–387.PubMed
56.
Zurück zum Zitat Bertolini, F., Martinelli, G., & Goldhirsch, A. (2001). Mosaic tumour blood vessels and high-dose chemotherapy for breast cancer. Lancet Oncology, 2(10), 595.PubMed Bertolini, F., Martinelli, G., & Goldhirsch, A. (2001). Mosaic tumour blood vessels and high-dose chemotherapy for breast cancer. Lancet Oncology, 2(10), 595.PubMed
57.
Zurück zum Zitat Chhieng, D. C., et al. (2003). Microvessel density and vascular endothelial growth factor expression in infiltrating lobular mammary carcinoma. The Breast Journal, 9(3), 200–207.PubMed Chhieng, D. C., et al. (2003). Microvessel density and vascular endothelial growth factor expression in infiltrating lobular mammary carcinoma. The Breast Journal, 9(3), 200–207.PubMed
58.
Zurück zum Zitat Dahut, W. L., et al. (2006). Phase I clinical trial of oral 2-methoxyestradiol, an antiangiogenic and apoptotic agent, in patients with solid tumors. Cancer Biology & Therapy, 5(1), 22–27. Dahut, W. L., et al. (2006). Phase I clinical trial of oral 2-methoxyestradiol, an antiangiogenic and apoptotic agent, in patients with solid tumors. Cancer Biology & Therapy, 5(1), 22–27.
59.
Zurück zum Zitat Dowlati, A., et al. (2005). Novel Phase I dose de-escalation design trial to determine the biological modulatory dose of the antiangiogenic agent SU5416. Clinical Cancer Research, 11(21), 7938–7944.PubMed Dowlati, A., et al. (2005). Novel Phase I dose de-escalation design trial to determine the biological modulatory dose of the antiangiogenic agent SU5416. Clinical Cancer Research, 11(21), 7938–7944.PubMed
60.
Zurück zum Zitat Singhal, S., et al. (1999). Antitumor activity of thalidomide in refractory multiple myeloma. The New England Journal of Medicine, 341(21), 1565–1571.PubMed Singhal, S., et al. (1999). Antitumor activity of thalidomide in refractory multiple myeloma. The New England Journal of Medicine, 341(21), 1565–1571.PubMed
61.
Zurück zum Zitat Wedam, S. B., et al. (2006). Antiangiogenic and antitumor effects of bevacizumab in patients with inflammatory and locally advanced breast cancer. Journal of Clinical Oncology, 24(5), 769–777.PubMed Wedam, S. B., et al. (2006). Antiangiogenic and antitumor effects of bevacizumab in patients with inflammatory and locally advanced breast cancer. Journal of Clinical Oncology, 24(5), 769–777.PubMed
62.
Zurück zum Zitat Miller, J. C., et al. (2005). Imaging angiogenesis: applications and potential for drug development. Journal of the National Cancer Institute, 97(3), 172–187.PubMed Miller, J. C., et al. (2005). Imaging angiogenesis: applications and potential for drug development. Journal of the National Cancer Institute, 97(3), 172–187.PubMed
63.
Zurück zum Zitat Soo, R. A., et al. (2006). Celecoxib reduces microvessel density in patients treated with nasopharyngeal carcinoma and induces changes in gene expression. Annals of Oncology, 17(11), 1625–1630.PubMed Soo, R. A., et al. (2006). Celecoxib reduces microvessel density in patients treated with nasopharyngeal carcinoma and induces changes in gene expression. Annals of Oncology, 17(11), 1625–1630.PubMed
64.
Zurück zum Zitat Zhou, Y., et al. (2007). Effect of celecoxib on E-cadherin, VEGF, Microvessel density and apoptosis in gastric cancer. Cancer Biology & Therapy, 6(2), 269–275. Zhou, Y., et al. (2007). Effect of celecoxib on E-cadherin, VEGF, Microvessel density and apoptosis in gastric cancer. Cancer Biology & Therapy, 6(2), 269–275.
65.
Zurück zum Zitat Ruegg, C., et al. (2003). The quest for surrogate markers of angiogenesis: A paradigm for translational research in tumor angiogenesis and anti-angiogenesis trials. Current Molecular Medicine, 3(8), 673–691.PubMed Ruegg, C., et al. (2003). The quest for surrogate markers of angiogenesis: A paradigm for translational research in tumor angiogenesis and anti-angiogenesis trials. Current Molecular Medicine, 3(8), 673–691.PubMed
66.
Zurück zum Zitat Schor, A. M., et al. (1998). Heterogeneity in microvascular density in lung tumours: Comparison with normal bronchus. British Journal of Cancer, 77(6), 946–951.PubMed Schor, A. M., et al. (1998). Heterogeneity in microvascular density in lung tumours: Comparison with normal bronchus. British Journal of Cancer, 77(6), 946–951.PubMed
67.
Zurück zum Zitat Dales, J. P., et al. (2004). Prognostic significance of angiogenesis evaluated by CD105 expression compared to CD31 in 905 breast carcinomas: Correlation with long-term patient outcome. International Journal of Oncology, 24(5), 1197–1204.PubMed Dales, J. P., et al. (2004). Prognostic significance of angiogenesis evaluated by CD105 expression compared to CD31 in 905 breast carcinomas: Correlation with long-term patient outcome. International Journal of Oncology, 24(5), 1197–1204.PubMed
68.
Zurück zum Zitat Duff, S. E., et al. (2003). CD105 is important for angiogenesis: Evidence and potential applications. The FASEB Journal, 17(9), 984–992.PubMed Duff, S. E., et al. (2003). CD105 is important for angiogenesis: Evidence and potential applications. The FASEB Journal, 17(9), 984–992.PubMed
69.
Zurück zum Zitat Kumar, S., et al. (1999). Breast carcinoma: Vascular density determined using CD105 antibody correlates with tumor prognosis. Cancer Research, 59(4), 856–861.PubMed Kumar, S., et al. (1999). Breast carcinoma: Vascular density determined using CD105 antibody correlates with tumor prognosis. Cancer Research, 59(4), 856–861.PubMed
70.
Zurück zum Zitat Tanaka, F., et al. (2001). Evaluation of angiogenesis in non-small cell lung cancer: Comparison between anti-CD34 antibody and anti-CD105 antibody. Clinical Cancer Research, 7(11), 3410–3415.PubMed Tanaka, F., et al. (2001). Evaluation of angiogenesis in non-small cell lung cancer: Comparison between anti-CD34 antibody and anti-CD105 antibody. Clinical Cancer Research, 7(11), 3410–3415.PubMed
71.
Zurück zum Zitat Sharma, S., Sharma, M. C., & Sarkar, C. (2005). Morphology of angiogenesis in human cancer: A conceptual overview, histoprognostic perspective and significance of neoangiogenesis. Histopathology, 46(5), 481–489.PubMed Sharma, S., Sharma, M. C., & Sarkar, C. (2005). Morphology of angiogenesis in human cancer: A conceptual overview, histoprognostic perspective and significance of neoangiogenesis. Histopathology, 46(5), 481–489.PubMed
72.
Zurück zum Zitat Algire, G. H., Chalkley, H. W., Legallais, F. Y., & Park, H. D. (1945). Vascular reactions of normal and malignant tissues in vivo. I. Vascular reactions of mice to wounds and to normal and neoplastic transplants. Journal of the National Cancer Institute, 6, 73–85. Algire, G. H., Chalkley, H. W., Legallais, F. Y., & Park, H. D. (1945). Vascular reactions of normal and malignant tissues in vivo. I. Vascular reactions of mice to wounds and to normal and neoplastic transplants. Journal of the National Cancer Institute, 6, 73–85.
73.
Zurück zum Zitat Vogel, A. W. (1965). Intratumoral vascular changes with increased size of a mammary adenocarcinoma: New method and results. Journal of the National Cancer Institute, 34, 571–578.PubMed Vogel, A. W. (1965). Intratumoral vascular changes with increased size of a mammary adenocarcinoma: New method and results. Journal of the National Cancer Institute, 34, 571–578.PubMed
74.
Zurück zum Zitat Hilmas, D. E., & Gillette, E. L. (1975). Tumor microvasculature following fractionated x irradiation. Radiology, 116(1), 165–169.PubMed Hilmas, D. E., & Gillette, E. L. (1975). Tumor microvasculature following fractionated x irradiation. Radiology, 116(1), 165–169.PubMed
75.
Zurück zum Zitat Kadambi, A., et al. (2001). Vascular endothelial growth factor (VEGF)-C differentially affects tumor vascular function and leukocyte recruitment: Role of VEGF-receptor 2 and host VEGF-A. Cancer Research, 61(6), 2404–2408.PubMed Kadambi, A., et al. (2001). Vascular endothelial growth factor (VEGF)-C differentially affects tumor vascular function and leukocyte recruitment: Role of VEGF-receptor 2 and host VEGF-A. Cancer Research, 61(6), 2404–2408.PubMed
76.
Zurück zum Zitat Cho, W. C., & Cheng, C. H. (2007). Oncoproteomics: Current trends and future perspectives. Expert Review of Proteomics, 4(3), 401–410.PubMed Cho, W. C., & Cheng, C. H. (2007). Oncoproteomics: Current trends and future perspectives. Expert Review of Proteomics, 4(3), 401–410.PubMed
77.
Zurück zum Zitat Mittal, V., & Nolan, D. J. (2007). Genomics and proteomics approaches in understanding tumor angiogenesis. Expert Review of Molecular Diagnostics, 7(2), 133–147.PubMed Mittal, V., & Nolan, D. J. (2007). Genomics and proteomics approaches in understanding tumor angiogenesis. Expert Review of Molecular Diagnostics, 7(2), 133–147.PubMed
78.
Zurück zum Zitat Petricoin, E. F., & Liotta, L. A. (2004). Proteomic approaches in cancer risk and response assessment. Trends in Molecular Medicine, 10(2), 59–64.PubMed Petricoin, E. F., & Liotta, L. A. (2004). Proteomic approaches in cancer risk and response assessment. Trends in Molecular Medicine, 10(2), 59–64.PubMed
79.
Zurück zum Zitat Alexander, H., et al. (2004). Proteomic analysis to identify breast cancer biomarkers in nipple aspirate fluid. Clinical Cancer Research, 10(22), 7500–7510.PubMed Alexander, H., et al. (2004). Proteomic analysis to identify breast cancer biomarkers in nipple aspirate fluid. Clinical Cancer Research, 10(22), 7500–7510.PubMed
80.
Zurück zum Zitat Bhattacharyya, S., et al. (2004). Diagnosis of pancreatic cancer using serum proteomic profiling. Neoplasia, 6(5), 674–686.PubMed Bhattacharyya, S., et al. (2004). Diagnosis of pancreatic cancer using serum proteomic profiling. Neoplasia, 6(5), 674–686.PubMed
81.
Zurück zum Zitat Petricoin, E. F., et al. (2002). Use of proteomic patterns in serum to identify ovarian cancer. Lancet, 359(9306), 572–577.PubMed Petricoin, E. F., et al. (2002). Use of proteomic patterns in serum to identify ovarian cancer. Lancet, 359(9306), 572–577.PubMed
82.
Zurück zum Zitat Petricoin 3rd, E. F., et al. (2002). Serum proteomic patterns for detection of prostate cancer. Journal of the National Cancer Institute, 94(20), 1576–1578.PubMed Petricoin 3rd, E. F., et al. (2002). Serum proteomic patterns for detection of prostate cancer. Journal of the National Cancer Institute, 94(20), 1576–1578.PubMed
83.
Zurück zum Zitat Conrads, T. P., et al. (2004). Proteomic patterns as a diagnostic tool for early-stage cancer: A review of its progress to a clinically relevant tool. Molecular Diagnosis, 8(2), 77–85.PubMed Conrads, T. P., et al. (2004). Proteomic patterns as a diagnostic tool for early-stage cancer: A review of its progress to a clinically relevant tool. Molecular Diagnosis, 8(2), 77–85.PubMed
84.
Zurück zum Zitat Kuerer, H. M., et al. (2004). Association between ductal fluid proteomic expression profiles and the presence of lymph node metastases in women with breast cancer. Surgery, 136(5), 1061–1069.PubMed Kuerer, H. M., et al. (2004). Association between ductal fluid proteomic expression profiles and the presence of lymph node metastases in women with breast cancer. Surgery, 136(5), 1061–1069.PubMed
85.
Zurück zum Zitat Pusztai, L., et al. (2004). Pharmacoproteomic analysis of prechemotherapy and postchemotherapy plasma samples from patients receiving neoadjuvant or adjuvant chemotherapy for breast carcinoma. Cancer, 100(9), 1814–1822.PubMed Pusztai, L., et al. (2004). Pharmacoproteomic analysis of prechemotherapy and postchemotherapy plasma samples from patients receiving neoadjuvant or adjuvant chemotherapy for breast carcinoma. Cancer, 100(9), 1814–1822.PubMed
86.
Zurück zum Zitat Bouamrani, A., et al. (2006). Direct-tissue SELDI-TOF mass spectrometry analysis: A new application for clinical proteomics. Clinical Chemistry, 52(11), 2103–2106.PubMed Bouamrani, A., et al. (2006). Direct-tissue SELDI-TOF mass spectrometry analysis: A new application for clinical proteomics. Clinical Chemistry, 52(11), 2103–2106.PubMed
87.
Zurück zum Zitat Hwang, S. I., et al. (2007). Direct cancer tissue proteomics: a method to identify candidate cancer biomarkers from formalin-fixed paraffin-embedded archival tissues. Oncogene, 26(1), 65–76.PubMed Hwang, S. I., et al. (2007). Direct cancer tissue proteomics: a method to identify candidate cancer biomarkers from formalin-fixed paraffin-embedded archival tissues. Oncogene, 26(1), 65–76.PubMed
88.
Zurück zum Zitat Irish, J. M., Kotecha, N., & Nolan, G. P. (2006). Mapping normal and cancer cell signalling networks: Towards single-cell proteomics. Nature Reviews. Cancer, 6(2), 146–155.PubMed Irish, J. M., Kotecha, N., & Nolan, G. P. (2006). Mapping normal and cancer cell signalling networks: Towards single-cell proteomics. Nature Reviews. Cancer, 6(2), 146–155.PubMed
89.
Zurück zum Zitat Tarnok, A., Bocsi, J., & Brockhoff, G. (2006). Cytomics—importance of multimodal analysis of cell function and proliferation in oncology. Cell Proliferation, 39(6), 495–505.PubMed Tarnok, A., Bocsi, J., & Brockhoff, G. (2006). Cytomics—importance of multimodal analysis of cell function and proliferation in oncology. Cell Proliferation, 39(6), 495–505.PubMed
90.
Zurück zum Zitat Ornstein, D. K., & Petricoin 3rd, E. F. (2004). Proteomics to diagnose human tumors and provide prognostic information. Oncology (Williston Park), 18(4), 521–529 discussion 529–32. Ornstein, D. K., & Petricoin 3rd, E. F. (2004). Proteomics to diagnose human tumors and provide prognostic information. Oncology (Williston Park), 18(4), 521–529 discussion 529–32.
91.
Zurück zum Zitat Reid, J. D., Parker, C. E., & Borchers, C. H. (2007). Protein arrays for biomarker discovery. Current Opinion in Molecular Therapeutics, 9(3), 216–221.PubMed Reid, J. D., Parker, C. E., & Borchers, C. H. (2007). Protein arrays for biomarker discovery. Current Opinion in Molecular Therapeutics, 9(3), 216–221.PubMed
92.
Zurück zum Zitat Adachi, J., et al. (2006). The human urinary proteome contains more than 1500 proteins, including a large proportion of membrane proteins. Genome Biology, 7(9), R80.PubMed Adachi, J., et al. (2006). The human urinary proteome contains more than 1500 proteins, including a large proportion of membrane proteins. Genome Biology, 7(9), R80.PubMed
93.
Zurück zum Zitat Venable, J. D., et al. (2007). Relative quantification of stable isotope labeled peptides using a linear ion trap-Orbitrap hybrid mass spectrometer. Analytical Chemistry, 79(8), 3056–3064.PubMed Venable, J. D., et al. (2007). Relative quantification of stable isotope labeled peptides using a linear ion trap-Orbitrap hybrid mass spectrometer. Analytical Chemistry, 79(8), 3056–3064.PubMed
94.
Zurück zum Zitat Imami, K., et al. (2007). Simple on-line sample preconcentration technique for peptides based on dynamic pH junction in capillary electrophoresis-mass spectrometry. Journal of Chromatography A, 1148(2), 250–255.PubMed Imami, K., et al. (2007). Simple on-line sample preconcentration technique for peptides based on dynamic pH junction in capillary electrophoresis-mass spectrometry. Journal of Chromatography A, 1148(2), 250–255.PubMed
95.
Zurück zum Zitat Bruneel, A., et al. (2005). Proteomics of human umbilical vein endothelial cells applied to etoposide-induced apoptosis. Proteomics, 5(15), 3876–3884.PubMed Bruneel, A., et al. (2005). Proteomics of human umbilical vein endothelial cells applied to etoposide-induced apoptosis. Proteomics, 5(15), 3876–3884.PubMed
96.
Zurück zum Zitat Chen, R., et al. (2005). Pancreatic cancer proteome: The proteins that underlie invasion, metastasis, and immunologic escape. Gastroenterology, 129(4), 1187–1197.PubMed Chen, R., et al. (2005). Pancreatic cancer proteome: The proteins that underlie invasion, metastasis, and immunologic escape. Gastroenterology, 129(4), 1187–1197.PubMed
97.
Zurück zum Zitat Shen, F., et al. (2006). Functional proteometrics for cell migration. Cytometry A, 69(7), 563–572.PubMed Shen, F., et al. (2006). Functional proteometrics for cell migration. Cytometry A, 69(7), 563–572.PubMed
98.
Zurück zum Zitat Shen, J., et al. (2006). Identification and validation of differences in protein levels in normal, premalignant, and malignant lung cells and tissues using high-throughput western array and immunohistochemistry. Cancer Research, 66(23), 11194–11206.PubMed Shen, J., et al. (2006). Identification and validation of differences in protein levels in normal, premalignant, and malignant lung cells and tissues using high-throughput western array and immunohistochemistry. Cancer Research, 66(23), 11194–11206.PubMed
99.
Zurück zum Zitat Thompson, L. P., & Dong, Y. (2005). Chronic hypoxia decreases endothelial nitric oxide synthase protein expression in fetal guinea pig hearts. Journal of the Society for Gynecologic Investigation, 12(6), 388–395.PubMed Thompson, L. P., & Dong, Y. (2005). Chronic hypoxia decreases endothelial nitric oxide synthase protein expression in fetal guinea pig hearts. Journal of the Society for Gynecologic Investigation, 12(6), 388–395.PubMed
100.
Zurück zum Zitat Oh, P., et al. (2004). Subtractive proteomic mapping of the endothelial surface in lung and solid tumours for tissue-specific therapy. Nature, 429(6992), 629–635.PubMed Oh, P., et al. (2004). Subtractive proteomic mapping of the endothelial surface in lung and solid tumours for tissue-specific therapy. Nature, 429(6992), 629–635.PubMed
101.
Zurück zum Zitat Mustafa, D. A. N., et al. (2007). Identification of glioma neovascularization-related proteins by using MALDI-FTMS and Nano-LC fractionation to microdissected tumor vessels. Molecular & Cellular Proteomics, 6(7), 1147–1157. Mustafa, D. A. N., et al. (2007). Identification of glioma neovascularization-related proteins by using MALDI-FTMS and Nano-LC fractionation to microdissected tumor vessels. Molecular & Cellular Proteomics, 6(7), 1147–1157.
102.
Zurück zum Zitat Christian, S., et al. (2003). Nucleolin expressed at the cell surface is a marker of endothelial cells in angiogenic blood vessels. The Journal of Cell Biology, 163(4), 871–878.PubMed Christian, S., et al. (2003). Nucleolin expressed at the cell surface is a marker of endothelial cells in angiogenic blood vessels. The Journal of Cell Biology, 163(4), 871–878.PubMed
103.
Zurück zum Zitat Hu, J., et al. (2005). Gene expression signature for angiogenic and nonangiogenic non-small-cell lung cancer. Oncogene, 24(7), 1212–1219.PubMed Hu, J., et al. (2005). Gene expression signature for angiogenic and nonangiogenic non-small-cell lung cancer. Oncogene, 24(7), 1212–1219.PubMed
104.
Zurück zum Zitat Croix, B. S., et al. (2000). Genes expressed in human tumor endothelium. Science, 289(5482), 1197–1202. Croix, B. S., et al. (2000). Genes expressed in human tumor endothelium. Science, 289(5482), 1197–1202.
105.
Zurück zum Zitat Seaman, S., et al. (2007). Genes that distinguish physiological and pathological angiogenesis. Cancer Cell, 11(6), 539–554.PubMed Seaman, S., et al. (2007). Genes that distinguish physiological and pathological angiogenesis. Cancer Cell, 11(6), 539–554.PubMed
106.
Zurück zum Zitat Li, J.-L., & Harris, A. L. (2007). The potential of new tumor endothelium-specific markers for the development of antivascular therapy. Cancer Cell, 11(6), 478–481.PubMed Li, J.-L., & Harris, A. L. (2007). The potential of new tumor endothelium-specific markers for the development of antivascular therapy. Cancer Cell, 11(6), 478–481.PubMed
107.
Zurück zum Zitat Nanda, A., & St Croix, B. (2004). Tumor endothelial markers: New targets for cancer therapy. Current Opinion in Oncology, 16(1), 44–49.PubMed Nanda, A., & St Croix, B. (2004). Tumor endothelial markers: New targets for cancer therapy. Current Opinion in Oncology, 16(1), 44–49.PubMed
108.
Zurück zum Zitat Beaty, R., et al. (2007). PLXDC1 (TEM7) is identified in a genome-wide expression screen of glioblastoma endothelium. Journal of Neuro-Oncology, 81(3), 241–248.PubMed Beaty, R., et al. (2007). PLXDC1 (TEM7) is identified in a genome-wide expression screen of glioblastoma endothelium. Journal of Neuro-Oncology, 81(3), 241–248.PubMed
109.
Zurück zum Zitat Madden, S. L., et al. (2004). Vascular gene expression in nonneoplastic and malignant brain. The American Journal of Pathology, 165(2), 601–608.PubMed Madden, S. L., et al. (2004). Vascular gene expression in nonneoplastic and malignant brain. The American Journal of Pathology, 165(2), 601–608.PubMed
110.
Zurück zum Zitat Parker, B. S., et al. (2004). Alterations in vascular gene expression in invasive breast carcinoma. Cancer Research, 64(21), 7857–7866.PubMed Parker, B. S., et al. (2004). Alterations in vascular gene expression in invasive breast carcinoma. Cancer Research, 64(21), 7857–7866.PubMed
111.
Zurück zum Zitat Ho, M., et al. (2003). Identification of endothelial cell genes by combined database mining and microarray analysis. Physiological Genomics, 13(3), 249–262.PubMed Ho, M., et al. (2003). Identification of endothelial cell genes by combined database mining and microarray analysis. Physiological Genomics, 13(3), 249–262.PubMed
112.
Zurück zum Zitat Yang, X., & Sun, X. (2007). Meta-analysis of several gene lists for distinct types of cancer: A simple way to reveal common prognostic markers. BMC Bioinformatics, 8(1), 118.PubMed Yang, X., & Sun, X. (2007). Meta-analysis of several gene lists for distinct types of cancer: A simple way to reveal common prognostic markers. BMC Bioinformatics, 8(1), 118.PubMed
113.
Zurück zum Zitat Costouros, N. G., et al. (2002). Microarray gene expression analysis of murine tumor heterogeneity defined by dynamic contrast-enhanced MRI. Molecular Imaging, 1(3), 301–308.PubMed Costouros, N. G., et al. (2002). Microarray gene expression analysis of murine tumor heterogeneity defined by dynamic contrast-enhanced MRI. Molecular Imaging, 1(3), 301–308.PubMed
114.
Zurück zum Zitat Jackson, A., et al. (2007). Imaging tumor vascular heterogeneity and angiogenesis using dynamic contrast-enhanced magnetic resonance imaging. Clinical Cancer Research, 13(12), 3449–3459.PubMed Jackson, A., et al. (2007). Imaging tumor vascular heterogeneity and angiogenesis using dynamic contrast-enhanced magnetic resonance imaging. Clinical Cancer Research, 13(12), 3449–3459.PubMed
115.
Zurück zum Zitat Menard, C., et al. (2005). An interventional magnetic resonance imaging technique for the molecular characterization of intraprostatic dynamic contrast enhancement. Molecular Imaging, 4(1), 63–66.PubMed Menard, C., et al. (2005). An interventional magnetic resonance imaging technique for the molecular characterization of intraprostatic dynamic contrast enhancement. Molecular Imaging, 4(1), 63–66.PubMed
116.
Zurück zum Zitat Jaeger, J., et al. (2007). Gene expression signatures for tumor progression, tumor subtype, and tumor thickness in laser-microdissected melanoma tissues. Clinical Cancer Research, 13(3), 806–815.PubMed Jaeger, J., et al. (2007). Gene expression signatures for tumor progression, tumor subtype, and tumor thickness in laser-microdissected melanoma tissues. Clinical Cancer Research, 13(3), 806–815.PubMed
117.
Zurück zum Zitat Pen, A., et al. (2007). Molecular markers of extracellular matrix remodeling in glioblastoma vessels: Microarray study of laser-captured glioblastoma vessels. Glia, 55(6), 559–572.PubMed Pen, A., et al. (2007). Molecular markers of extracellular matrix remodeling in glioblastoma vessels: Microarray study of laser-captured glioblastoma vessels. Glia, 55(6), 559–572.PubMed
118.
Zurück zum Zitat Schuetz, C. S., et al. (2006). Progression-specific genes identified by expression profiling of matched ductal carcinomas in situ and invasive breast tumors, combining laser capture microdissection and oligonucleotide microarray analysis. Cancer Research, 66(10), 5278–5286.PubMed Schuetz, C. S., et al. (2006). Progression-specific genes identified by expression profiling of matched ductal carcinomas in situ and invasive breast tumors, combining laser capture microdissection and oligonucleotide microarray analysis. Cancer Research, 66(10), 5278–5286.PubMed
119.
Zurück zum Zitat Yang, F., et al. (2006). Laser microdissection and microarray analysis of breast tumors reveal ER-alpha related genes and pathways. Oncogene, 25(9), 1413–1419.PubMed Yang, F., et al. (2006). Laser microdissection and microarray analysis of breast tumors reveal ER-alpha related genes and pathways. Oncogene, 25(9), 1413–1419.PubMed
120.
Zurück zum Zitat Scappaticci, F. A., et al. (2005). Surgical wound healing complications in metastatic colorectal cancer patients treated with bevacizumab. Journal of Surgical Oncology, 91(3), 173–180.PubMed Scappaticci, F. A., et al. (2005). Surgical wound healing complications in metastatic colorectal cancer patients treated with bevacizumab. Journal of Surgical Oncology, 91(3), 173–180.PubMed
121.
Zurück zum Zitat Drevs, J., & Schneider, V. (2006). The use of vascular biomarkers and imaging studies in the early clinical development of anti-tumour agents targeting angiogenesis. Journal of Internal Medicine, 260(6), 517–529.PubMed Drevs, J., & Schneider, V. (2006). The use of vascular biomarkers and imaging studies in the early clinical development of anti-tumour agents targeting angiogenesis. Journal of Internal Medicine, 260(6), 517–529.PubMed
122.
Zurück zum Zitat Zhang, D., et al. (2007). Effects of a monoclonal anti-avb3 integrin antibody on blood vessels—A pharmacodynamic study. Investigational New Drugs, 25(1), 49–55.PubMed Zhang, D., et al. (2007). Effects of a monoclonal anti-avb3 integrin antibody on blood vessels—A pharmacodynamic study. Investigational New Drugs, 25(1), 49–55.PubMed
123.
Zurück zum Zitat Mundhenke, C., et al. (2001). Tissue examination to monitor antiangiogenic therapy: A phase I clinical trial with endostatin. Clinical Cancer Research, 7(11), 3366–3374.PubMed Mundhenke, C., et al. (2001). Tissue examination to monitor antiangiogenic therapy: A phase I clinical trial with endostatin. Clinical Cancer Research, 7(11), 3366–3374.PubMed
124.
Zurück zum Zitat Lockhart, A. C., et al. (2003). Reduction of wound angiogenesis in patients treated with BMS-275291, a broad spectrum matrix metalloproteinase inhibitor. Clinical Cancer Research, 9(2), 586–593.PubMed Lockhart, A. C., et al. (2003). Reduction of wound angiogenesis in patients treated with BMS-275291, a broad spectrum matrix metalloproteinase inhibitor. Clinical Cancer Research, 9(2), 586–593.PubMed
125.
Zurück zum Zitat Alvarez Secord, A., et al. (2004). The relationship between serum vascular endothelial growth factor, persistent disease, and survival at second-look laparotomy in ovarian cancer. Gynecologic Oncology, 94(1), 74–79.PubMed Alvarez Secord, A., et al. (2004). The relationship between serum vascular endothelial growth factor, persistent disease, and survival at second-look laparotomy in ovarian cancer. Gynecologic Oncology, 94(1), 74–79.PubMed
126.
Zurück zum Zitat Braybrooke, J. P., et al. (2000). A phase II study of razoxane, an antiangiogenic topoisomerase II inhibitor, in renal cell cancer with assessment of potential surrogate markers of angiogenesis. Clinical Cancer Research, 6(12), 4697–4704.PubMed Braybrooke, J. P., et al. (2000). A phase II study of razoxane, an antiangiogenic topoisomerase II inhibitor, in renal cell cancer with assessment of potential surrogate markers of angiogenesis. Clinical Cancer Research, 6(12), 4697–4704.PubMed
127.
Zurück zum Zitat Chan, L. W., et al. (2004). Urinary VEGF and MMP levels as predictive markers of 1-year progression-free survival in cancer patients treated with radiation therapy: A longitudinal study of protein kinetics throughout tumor progression and therapy. Journal of Clinical Oncology, 22(3), 499–506.PubMed Chan, L. W., et al. (2004). Urinary VEGF and MMP levels as predictive markers of 1-year progression-free survival in cancer patients treated with radiation therapy: A longitudinal study of protein kinetics throughout tumor progression and therapy. Journal of Clinical Oncology, 22(3), 499–506.PubMed
128.
Zurück zum Zitat Coskun, U., et al. (2003). Significance of serum vascular endothelial growth factor, insulin-like growth factor-I levels and nitric oxide activity in breast cancer patients. Breast, 12(2), 104–110.PubMed Coskun, U., et al. (2003). Significance of serum vascular endothelial growth factor, insulin-like growth factor-I levels and nitric oxide activity in breast cancer patients. Breast, 12(2), 104–110.PubMed
129.
Zurück zum Zitat Duque, J. L., et al. (2006). Measurement of plasma levels of vascular endothelial growth factor in prostate cancer patients: Relationship with clinical stage, Gleason score, prostate volume, and serum prostate-specific antigen. Clinics, 61(5), 401–408.PubMed Duque, J. L., et al. (2006). Measurement of plasma levels of vascular endothelial growth factor in prostate cancer patients: Relationship with clinical stage, Gleason score, prostate volume, and serum prostate-specific antigen. Clinics, 61(5), 401–408.PubMed
130.
Zurück zum Zitat Fine, H. A., et al. (2000). Phase II trial of the antiangiogenic agent thalidomide in patients with recurrent high-grade gliomas. Journal of Clinical Oncology, 18(4), 708–715.PubMed Fine, H. A., et al. (2000). Phase II trial of the antiangiogenic agent thalidomide in patients with recurrent high-grade gliomas. Journal of Clinical Oncology, 18(4), 708–715.PubMed
131.
Zurück zum Zitat Kaya, A., et al. (2004). The prognostic significance of vascular endothelial growth factor levels in sera of non-small cell lung cancer patients. Respiratory Medicine, 98(7), 632–636.PubMed Kaya, A., et al. (2004). The prognostic significance of vascular endothelial growth factor levels in sera of non-small cell lung cancer patients. Respiratory Medicine, 98(7), 632–636.PubMed
132.
Zurück zum Zitat Krzystek-Korpacka, M., et al. (2007). Up-regulation of VEGF-C secreted by cancer cells and not VEGF-A correlates with clinical evaluation of lymph node metastasis in esophageal squamous cell carcinoma (ESCC). Cancer Letters, 249(2), 171–177.PubMed Krzystek-Korpacka, M., et al. (2007). Up-regulation of VEGF-C secreted by cancer cells and not VEGF-A correlates with clinical evaluation of lymph node metastasis in esophageal squamous cell carcinoma (ESCC). Cancer Letters, 249(2), 171–177.PubMed
133.
Zurück zum Zitat Li, L., et al. (2004). Correlation of serum VEGF levels with clinical stage, therapy efficacy, tumor metastasis and patient survival in ovarian cancer. Anticancer Research, 24(3b), 1973–1979.PubMed Li, L., et al. (2004). Correlation of serum VEGF levels with clinical stage, therapy efficacy, tumor metastasis and patient survival in ovarian cancer. Anticancer Research, 24(3b), 1973–1979.PubMed
134.
Zurück zum Zitat Poon, R. T., et al. (2004). Prognostic significance of serum vascular endothelial growth factor and endostatin in patients with hepatocellular carcinoma. The British Journal of Surgery, 91(10), 1354–1360.PubMed Poon, R. T., et al. (2004). Prognostic significance of serum vascular endothelial growth factor and endostatin in patients with hepatocellular carcinoma. The British Journal of Surgery, 91(10), 1354–1360.PubMed
135.
Zurück zum Zitat Poon, R. T.-P., et al. (2003). Quantitative correlation of serum levels and tumor expression of vascular endothelial growth factor in patients with hepatocellular carcinoma. Cancer Research, 63(12), 3121–3126.PubMed Poon, R. T.-P., et al. (2003). Quantitative correlation of serum levels and tumor expression of vascular endothelial growth factor in patients with hepatocellular carcinoma. Cancer Research, 63(12), 3121–3126.PubMed
136.
Zurück zum Zitat Shariat, S. F., et al. (2004). Association of preoperative plasma levels of vascular endothelial growth factor and soluble vascular cell adhesion molecule-1 with lymph node status and biochemical progression after radical prostatectomy. Journal of Clinical Oncology, 22(9), 1655–1663.PubMed Shariat, S. F., et al. (2004). Association of preoperative plasma levels of vascular endothelial growth factor and soluble vascular cell adhesion molecule-1 with lymph node status and biochemical progression after radical prostatectomy. Journal of Clinical Oncology, 22(9), 1655–1663.PubMed
137.
Zurück zum Zitat Shariat, S. F., et al. (2004). Association of pre- and postoperative plasma levels of transforming growth factor beta(1) and interleukin 6 and its soluble receptor with prostate cancer progression. Clinical Cancer Research, 10(6), 1992–1999.PubMed Shariat, S. F., et al. (2004). Association of pre- and postoperative plasma levels of transforming growth factor beta(1) and interleukin 6 and its soluble receptor with prostate cancer progression. Clinical Cancer Research, 10(6), 1992–1999.PubMed
138.
Zurück zum Zitat Sliutz, G., et al. (1995). Serum evaluation of basic FGF in breast cancer patients. Anticancer Research, 15(6B), 2675–2677.PubMed Sliutz, G., et al. (1995). Serum evaluation of basic FGF in breast cancer patients. Anticancer Research, 15(6B), 2675–2677.PubMed
139.
Zurück zum Zitat Tamura, M., et al. (2004). Chest CT and serum vascular endothelial growth factor-C level to diagnose lymph node metastasis in patients with primary non-small cell lung cancer. Chest, 126(2), 342–346.PubMed Tamura, M., et al. (2004). Chest CT and serum vascular endothelial growth factor-C level to diagnose lymph node metastasis in patients with primary non-small cell lung cancer. Chest, 126(2), 342–346.PubMed
140.
Zurück zum Zitat Gonzalez, F. J., et al. (2007). Prognostic value of serum angiogenic activity in colorectal cancer patients. Journal of Cellular and Molecular Medicine, 11(1), 120–128.PubMed Gonzalez, F. J., et al. (2007). Prognostic value of serum angiogenic activity in colorectal cancer patients. Journal of Cellular and Molecular Medicine, 11(1), 120–128.PubMed
141.
Zurück zum Zitat Negrier, S., et al. (2004). Interleukin-6, interleukin-10, and vascular endothelial growth factor in metastatic renal cell carcinoma: Prognostic value of interleukin-6-from the Groupe Francais d’Immunotherapie. Journal of Clinical Oncology, 22(12), 2371–2378.PubMed Negrier, S., et al. (2004). Interleukin-6, interleukin-10, and vascular endothelial growth factor in metastatic renal cell carcinoma: Prognostic value of interleukin-6-from the Groupe Francais d’Immunotherapie. Journal of Clinical Oncology, 22(12), 2371–2378.PubMed
142.
Zurück zum Zitat Tas, F., et al. (2006). Serum vascular endothelial growth factor (VEGF) and bcl-2 levels in advanced stage non-small cell lung cancer. Cancer Investigation, 24(6), 576–580.PubMed Tas, F., et al. (2006). Serum vascular endothelial growth factor (VEGF) and bcl-2 levels in advanced stage non-small cell lung cancer. Cancer Investigation, 24(6), 576–580.PubMed
143.
Zurück zum Zitat Brostjan, C., et al. (2003). Monitoring of circulating angiogenic factors in dendritic cell-based cancer immunotherapy. Cancer, 98(10), 2291–2301.PubMed Brostjan, C., et al. (2003). Monitoring of circulating angiogenic factors in dendritic cell-based cancer immunotherapy. Cancer, 98(10), 2291–2301.PubMed
144.
Zurück zum Zitat Norden-Zfoni, A., et al. (2007). Blood-based biomarkers of SU11248 activity and clinical outcome in patients with metastatic imatinib-resistant gastrointestinal stromal tumor. Clinical Cancer Research, 13(9), 2643–2650.PubMed Norden-Zfoni, A., et al. (2007). Blood-based biomarkers of SU11248 activity and clinical outcome in patients with metastatic imatinib-resistant gastrointestinal stromal tumor. Clinical Cancer Research, 13(9), 2643–2650.PubMed
145.
Zurück zum Zitat Drevs, J., et al. (2007). Phase I clinical study of AZD2171, an oral vascular endothelial growth factor signaling inhibitor, in patients with advanced solid tumors. Journal of Clinical Oncology, 25(21), 3045–3054.PubMed Drevs, J., et al. (2007). Phase I clinical study of AZD2171, an oral vascular endothelial growth factor signaling inhibitor, in patients with advanced solid tumors. Journal of Clinical Oncology, 25(21), 3045–3054.PubMed
146.
Zurück zum Zitat Drevs, J. (2003). Soluble markers for the detection of hypoxia under antiangiogenic treatment. Anticancer Research, 23(2A), 1159–1161.PubMed Drevs, J. (2003). Soluble markers for the detection of hypoxia under antiangiogenic treatment. Anticancer Research, 23(2A), 1159–1161.PubMed
147.
Zurück zum Zitat Vincenzi, B., et al. (2007). Circulating VEGF reduction, response and outcome in advanced colorectal cancer patients treated with cetuximab plus irinotecan. Pharmacogenomics, 8(4), 319–327.PubMed Vincenzi, B., et al. (2007). Circulating VEGF reduction, response and outcome in advanced colorectal cancer patients treated with cetuximab plus irinotecan. Pharmacogenomics, 8(4), 319–327.PubMed
148.
Zurück zum Zitat Ria, R., et al. (2004). Serum levels of angiogenic cytokines decrease after antineoplastic radiotherapy. Cancer Letters, 216(1), 103–107.PubMed Ria, R., et al. (2004). Serum levels of angiogenic cytokines decrease after antineoplastic radiotherapy. Cancer Letters, 216(1), 103–107.PubMed
149.
Zurück zum Zitat Shimada, H., et al. (2002). Expression of angiogenic factors predicts response to chemoradiotherapy and prognosis of oesophageal squamous cell carcinoma. British Journal of Cancer, 86(4), 552–557.PubMed Shimada, H., et al. (2002). Expression of angiogenic factors predicts response to chemoradiotherapy and prognosis of oesophageal squamous cell carcinoma. British Journal of Cancer, 86(4), 552–557.PubMed
150.
Zurück zum Zitat Shimada, H., et al. (2001). Clinical significance of serum vascular endothelial growth factor in esophageal squamous cell carcinoma. Cancer, 92(3), 663–669.PubMed Shimada, H., et al. (2001). Clinical significance of serum vascular endothelial growth factor in esophageal squamous cell carcinoma. Cancer, 92(3), 663–669.PubMed
151.
Zurück zum Zitat Bewick, M., et al. (2004). Evaluation of sICAM-1, sVCAM-1, and sE-selectin levels in patients with metastatic breast cancer receiving high-dose chemotherapy. Stem Cells and Development, 13(3), 281–294.PubMed Bewick, M., et al. (2004). Evaluation of sICAM-1, sVCAM-1, and sE-selectin levels in patients with metastatic breast cancer receiving high-dose chemotherapy. Stem Cells and Development, 13(3), 281–294.PubMed
152.
Zurück zum Zitat Ding, Y. B., et al. (2003). Association of VCAM-1 overexpression with oncogenesis, tumor angiogenesis and metastasis of gastric carcinoma. World Journal of Gastroenterology, 9(7), 1409–1414.PubMed Ding, Y. B., et al. (2003). Association of VCAM-1 overexpression with oncogenesis, tumor angiogenesis and metastasis of gastric carcinoma. World Journal of Gastroenterology, 9(7), 1409–1414.PubMed
153.
Zurück zum Zitat Kumar, H., et al. (2002). Soluble FLT-1 is detectable in the sera of colorectal and breast cancer patients. Anticancer Research, 22(3), 1877–1880.PubMed Kumar, H., et al. (2002). Soluble FLT-1 is detectable in the sera of colorectal and breast cancer patients. Anticancer Research, 22(3), 1877–1880.PubMed
154.
Zurück zum Zitat Opala, T., et al. (2003). Evaluation of soluble intracellular adhesion molecule-1 (sICAM-1) in benign and malignant ovarian masses. European Journal of Gynaecological Oncology, 24(3–4), 255–257.PubMed Opala, T., et al. (2003). Evaluation of soluble intracellular adhesion molecule-1 (sICAM-1) in benign and malignant ovarian masses. European Journal of Gynaecological Oncology, 24(3–4), 255–257.PubMed
155.
Zurück zum Zitat Pasieka, Z., et al. (2004). Soluble intracellular adhesion molecules (sICAM-1, sVCAM-1) in peripheral blood of patients with thyroid cancer. Neoplasma, 51(1), 34–37.PubMed Pasieka, Z., et al. (2004). Soluble intracellular adhesion molecules (sICAM-1, sVCAM-1) in peripheral blood of patients with thyroid cancer. Neoplasma, 51(1), 34–37.PubMed
156.
Zurück zum Zitat Pasieka, Z., et al. (2003). Evaluation of the levels of bFGF, VEGF, sICAM-1, and sVCAM-1 in serum of patients with thyroid cancer. Recent Results in Cancer Research, 162, 189–194.PubMed Pasieka, Z., et al. (2003). Evaluation of the levels of bFGF, VEGF, sICAM-1, and sVCAM-1 in serum of patients with thyroid cancer. Recent Results in Cancer Research, 162, 189–194.PubMed
157.
Zurück zum Zitat Ishii, Y., & Kitamura, S. (1999). Soluble intercellular adhesion molecule-1 as an early detection marker for radiation pneumonitis. The European Respiratory Journal, 13(4), 733–738.PubMed Ishii, Y., & Kitamura, S. (1999). Soluble intercellular adhesion molecule-1 as an early detection marker for radiation pneumonitis. The European Respiratory Journal, 13(4), 733–738.PubMed
158.
Zurück zum Zitat Nordal, R. A., & Wong, C. S. (2004). Intercellular adhesion molecule-1 and blood-spinal cord barrier disruption in central nervous system radiation injury. Journal of Neuropathology and Experimental Neurology, 63(5), 474–483.PubMed Nordal, R. A., & Wong, C. S. (2004). Intercellular adhesion molecule-1 and blood-spinal cord barrier disruption in central nervous system radiation injury. Journal of Neuropathology and Experimental Neurology, 63(5), 474–483.PubMed
159.
Zurück zum Zitat Religa, P., et al. (2005). Presence of bone marrow-derived circulating progenitor endothelial cells in the newly formed lymphatic vessels. Blood, 106(13), 4184–4190.PubMed Religa, P., et al. (2005). Presence of bone marrow-derived circulating progenitor endothelial cells in the newly formed lymphatic vessels. Blood, 106(13), 4184–4190.PubMed
160.
Zurück zum Zitat Jansen, M., et al. (2004). Current perspectives on antiangiogenesis strategies in the treatment of malignant gliomas. Brain Research. Brain Research Reviews, 45(3), 143–163.PubMed Jansen, M., et al. (2004). Current perspectives on antiangiogenesis strategies in the treatment of malignant gliomas. Brain Research. Brain Research Reviews, 45(3), 143–163.PubMed
161.
Zurück zum Zitat Lyden, D., et al. (2001). Impaired recruitment of bone-marrow-derived endothelial and hematopoietic precursor cells blocks tumor angiogenesis and growth. Nature Medicine, 7(11), 1194–1201.PubMed Lyden, D., et al. (2001). Impaired recruitment of bone-marrow-derived endothelial and hematopoietic precursor cells blocks tumor angiogenesis and growth. Nature Medicine, 7(11), 1194–1201.PubMed
162.
Zurück zum Zitat Capillo, M., et al. (2003). Continuous infusion of endostatin inhibits differentiation, mobilization, and clonogenic potential of endothelial cell progenitors. Clinical Cancer Research, 9(1), 377–382.PubMed Capillo, M., et al. (2003). Continuous infusion of endostatin inhibits differentiation, mobilization, and clonogenic potential of endothelial cell progenitors. Clinical Cancer Research, 9(1), 377–382.PubMed
163.
Zurück zum Zitat Shaked, Y., et al. (2005). Genetic heterogeneity of the vasculogenic phenotype parallels angiogenesis: Implications for cellular surrogate marker analysis of antiangiogenesis. Cancer Cell, 7(1), 101–111.PubMed Shaked, Y., et al. (2005). Genetic heterogeneity of the vasculogenic phenotype parallels angiogenesis: Implications for cellular surrogate marker analysis of antiangiogenesis. Cancer Cell, 7(1), 101–111.PubMed
164.
Zurück zum Zitat Gill, M., et al. (2001). Vascular trauma induces rapid but transient mobilization of VEGFR2(+)AC133(+) endothelial precursor cells. Circulation Research, 88(2), 167–174.PubMed Gill, M., et al. (2001). Vascular trauma induces rapid but transient mobilization of VEGFR2(+)AC133(+) endothelial precursor cells. Circulation Research, 88(2), 167–174.PubMed
165.
Zurück zum Zitat Shintani, S., et al. (2001). Mobilization of endothelial progenitor cells in patients with acute myocardial infarction. Circulation, 103(23), 2776–2779.PubMed Shintani, S., et al. (2001). Mobilization of endothelial progenitor cells in patients with acute myocardial infarction. Circulation, 103(23), 2776–2779.PubMed
166.
Zurück zum Zitat Rabascio, C., et al. (2004). Assessing tumor angiogenesis: increased circulating VE-cadherin RNA in patients with cancer indicates viability of circulating endothelial cells. Cancer Research, 64(12), 4373–4377.PubMed Rabascio, C., et al. (2004). Assessing tumor angiogenesis: increased circulating VE-cadherin RNA in patients with cancer indicates viability of circulating endothelial cells. Cancer Research, 64(12), 4373–4377.PubMed
167.
Zurück zum Zitat Furstenberger, G., et al. (2006). Circulating endothelial cells and angiogenic serum factors during neoadjuvant chemotherapy of primary breast cancer. British Journal of Cancer, 94(4), 524–531.PubMed Furstenberger, G., et al. (2006). Circulating endothelial cells and angiogenic serum factors during neoadjuvant chemotherapy of primary breast cancer. British Journal of Cancer, 94(4), 524–531.PubMed
168.
Zurück zum Zitat Ocak, I., et al. (2007). The biologic basis of in vivo angiogenesis imaging. Frontiers in Bioscience, 12, 3601–3616.PubMed Ocak, I., et al. (2007). The biologic basis of in vivo angiogenesis imaging. Frontiers in Bioscience, 12, 3601–3616.PubMed
169.
Zurück zum Zitat Provenzale, J. M. (2007). Imaging of angiogenesis: Clinical techniques and novel imaging methods. AJR. American Journal of Roentgenology, 188(1), 11–23.PubMed Provenzale, J. M. (2007). Imaging of angiogenesis: Clinical techniques and novel imaging methods. AJR. American Journal of Roentgenology, 188(1), 11–23.PubMed
170.
Zurück zum Zitat Schirner, M., et al. (2004). Molecular imaging of tumor angiogenesis. Annals of the New York Academy of Sciences, 1014(1), 67–75.PubMed Schirner, M., et al. (2004). Molecular imaging of tumor angiogenesis. Annals of the New York Academy of Sciences, 1014(1), 67–75.PubMed
171.
Zurück zum Zitat Herbst, R. S., et al. (2002). Development of biologic markers of response and assessment of antiangiogenic activity in a clinical trial of human recombinant endostatin. Journal of Clinical Oncology, 20(18), 3804–3814.PubMed Herbst, R. S., et al. (2002). Development of biologic markers of response and assessment of antiangiogenic activity in a clinical trial of human recombinant endostatin. Journal of Clinical Oncology, 20(18), 3804–3814.PubMed
172.
Zurück zum Zitat Jennens, R., et al. (2004). Complete radiological and metabolic response of metastatic renal cell carcinoma to SU5416 (semaxanib) in a patient with probable von Hippel–Lindau syndrome. Urologic Oncology, 22(3), 193–196.PubMed Jennens, R., et al. (2004). Complete radiological and metabolic response of metastatic renal cell carcinoma to SU5416 (semaxanib) in a patient with probable von Hippel–Lindau syndrome. Urologic Oncology, 22(3), 193–196.PubMed
173.
Zurück zum Zitat Mullamitha, S. A., et al. (2007). Phase I evaluation of a fully human anti-{alpha}v integrin monoclonal antibody (CNTO 95) in patients with advanced solid tumors. Clinical Cancer Research, 13(7), 2128–2135.PubMed Mullamitha, S. A., et al. (2007). Phase I evaluation of a fully human anti-{alpha}v integrin monoclonal antibody (CNTO 95) in patients with advanced solid tumors. Clinical Cancer Research, 13(7), 2128–2135.PubMed
174.
Zurück zum Zitat Turner, C. D., et al. (2007). Phase II study of thalidomide and radiation in children with newly diagnosed brain stem gliomas and glioblastoma multiforme. Journal of Neurooncology, 82(1), 95–101. Turner, C. D., et al. (2007). Phase II study of thalidomide and radiation in children with newly diagnosed brain stem gliomas and glioblastoma multiforme. Journal of Neurooncology, 82(1), 95–101.
175.
Zurück zum Zitat Willett, C. G., et al. (2007). Complete pathological response to bevacizumab and chemoradiation in advanced rectal cancer. Nature Clinical Practice. Oncology, 4(5), 316–321.PubMed Willett, C. G., et al. (2007). Complete pathological response to bevacizumab and chemoradiation in advanced rectal cancer. Nature Clinical Practice. Oncology, 4(5), 316–321.PubMed
176.
Zurück zum Zitat Clavo, A., Brown, R., & Wahl, R. (1995). Fluorodeoxyglucose uptake in human cancer cell lines is increased by hypoxia. Journal of Nuclear Medicine, 36(9), 1625–1632.PubMed Clavo, A., Brown, R., & Wahl, R. (1995). Fluorodeoxyglucose uptake in human cancer cell lines is increased by hypoxia. Journal of Nuclear Medicine, 36(9), 1625–1632.PubMed
177.
Zurück zum Zitat Sivitz, W. I., et al. (1992). Pretranslational regulation of two cardiac glucose transporters in rats exposed to hypobaric hypoxia. American Journal of Physiology: Endocrinology and Metabolism, 263(3), E562–E569. Sivitz, W. I., et al. (1992). Pretranslational regulation of two cardiac glucose transporters in rats exposed to hypobaric hypoxia. American Journal of Physiology: Endocrinology and Metabolism, 263(3), E562–E569.
178.
Zurück zum Zitat McDonald, D. M., & Choyke, P. L. (2003). Imaging of angiogenesis: From microscope to clinic. Nature Medicine, 9(6), 713–725.PubMed McDonald, D. M., & Choyke, P. L. (2003). Imaging of angiogenesis: From microscope to clinic. Nature Medicine, 9(6), 713–725.PubMed
179.
Zurück zum Zitat Eschmann, S. M., et al. (2005). Prognostic impact of hypoxia imaging with 18F-misonidazole PET in non-small cell lung cancer and head and neck cancer before radiotherapy. Journal of Nuclear Medicine, 46(2), 253–260.PubMed Eschmann, S. M., et al. (2005). Prognostic impact of hypoxia imaging with 18F-misonidazole PET in non-small cell lung cancer and head and neck cancer before radiotherapy. Journal of Nuclear Medicine, 46(2), 253–260.PubMed
180.
Zurück zum Zitat Gagel, B., et al. (2006). [18F] fluoromisonidazole and [18F] fluorodeoxyglucose positron emission tomography in response evaluation after chemo-/radiotherapy of non-small-cell lung cancer: a feasibility study. BMC Cancer, 6, 51.PubMed Gagel, B., et al. (2006). [18F] fluoromisonidazole and [18F] fluorodeoxyglucose positron emission tomography in response evaluation after chemo-/radiotherapy of non-small-cell lung cancer: a feasibility study. BMC Cancer, 6, 51.PubMed
181.
Zurück zum Zitat Laking, G. R., & Price, P. M. (2003). Positron emission tomographic imaging of angiogenesis and vascular function. British Journal of Radiology, 76(suppl_1), S50–S59.PubMed Laking, G. R., & Price, P. M. (2003). Positron emission tomographic imaging of angiogenesis and vascular function. British Journal of Radiology, 76(suppl_1), S50–S59.PubMed
182.
Zurück zum Zitat Thorwarth, D., et al. (2005). A kinetic model for dynamic [18F]-Fmiso PET data to analyse tumour hypoxia. Physics in Medicine & Biology, 50(10), 2209–2224. Thorwarth, D., et al. (2005). A kinetic model for dynamic [18F]-Fmiso PET data to analyse tumour hypoxia. Physics in Medicine & Biology, 50(10), 2209–2224.
183.
Zurück zum Zitat Thorwarth, D., et al. (2005). Kinetic analysis of dynamic 18F-fluoromisonidazole PET correlates with radiation treatment outcome in head-and-neck cancer. BMC Cancer, 5, 152.PubMed Thorwarth, D., et al. (2005). Kinetic analysis of dynamic 18F-fluoromisonidazole PET correlates with radiation treatment outcome in head-and-neck cancer. BMC Cancer, 5, 152.PubMed
184.
Zurück zum Zitat Cher, L. M., et al. (2006). Correlation of hypoxic cell fraction and angiogenesis with glucose metabolic rate in gliomas using 18F-fluoromisonidazole, 18F-FDG PET, and Immunohistochemical Studies. Journal of Nuclear Medicine, 47(3), 410–418.PubMed Cher, L. M., et al. (2006). Correlation of hypoxic cell fraction and angiogenesis with glucose metabolic rate in gliomas using 18F-fluoromisonidazole, 18F-FDG PET, and Immunohistochemical Studies. Journal of Nuclear Medicine, 47(3), 410–418.PubMed
185.
Zurück zum Zitat Hicks, R. J., et al. (2005). Utility of FMISO PET in advanced head and neck cancer treated with chemoradiation incorporating a hypoxia-targeting chemotherapy agent. European Journal of Nuclear Medicine and Molecular Imaging, 32(12), 1384–1391.PubMed Hicks, R. J., et al. (2005). Utility of FMISO PET in advanced head and neck cancer treated with chemoradiation incorporating a hypoxia-targeting chemotherapy agent. European Journal of Nuclear Medicine and Molecular Imaging, 32(12), 1384–1391.PubMed
186.
Zurück zum Zitat Rischin, D., et al. (2006). Prognostic significance of [18F]-misonidazole positron emission tomography-detected tumor hypoxia in patients with advanced head and neck cancer randomly assigned to chemoradiation with or without tirapazamine: A substudy of Trans-Tasman Radiation Oncology Group Study 98.02. Journal of Clinical Oncology, 24(13), 2098–2104.PubMed Rischin, D., et al. (2006). Prognostic significance of [18F]-misonidazole positron emission tomography-detected tumor hypoxia in patients with advanced head and neck cancer randomly assigned to chemoradiation with or without tirapazamine: A substudy of Trans-Tasman Radiation Oncology Group Study 98.02. Journal of Clinical Oncology, 24(13), 2098–2104.PubMed
187.
Zurück zum Zitat Rischin, D., et al. (2001). Phase I trial of concurrent tirapazamine, cisplatin, and radiotherapy in patients with advanced head and neck cancer. Journal of Clinical Oncology, 19(2), 535–542.PubMed Rischin, D., et al. (2001). Phase I trial of concurrent tirapazamine, cisplatin, and radiotherapy in patients with advanced head and neck cancer. Journal of Clinical Oncology, 19(2), 535–542.PubMed
188.
Zurück zum Zitat Pal, A., et al. (2006). Molecular imaging of EGFR kinase activity in tumors with 124I-labeled small molecular tracer and positron emission tomography. Molecular Imaging and Biology, 8(5), 262–277.PubMed Pal, A., et al. (2006). Molecular imaging of EGFR kinase activity in tumors with 124I-labeled small molecular tracer and positron emission tomography. Molecular Imaging and Biology, 8(5), 262–277.PubMed
189.
Zurück zum Zitat Schmidt, K., et al. (2006). Angiostatin overexpression in Morris hepatoma results in decreased tumor growth but increased perfusion and vascularization. Journal of Nuclear Medicine, 47(3), 543–551.PubMed Schmidt, K., et al. (2006). Angiostatin overexpression in Morris hepatoma results in decreased tumor growth but increased perfusion and vascularization. Journal of Nuclear Medicine, 47(3), 543–551.PubMed
190.
Zurück zum Zitat Anderson, H., et al. (2003). Measurement of renal tumour and normal tissue perfusion using positron emission tomography in a phase II clinical trial of razoxane. British Journal of Cancer, 89(2), 262–267.PubMed Anderson, H., et al. (2003). Measurement of renal tumour and normal tissue perfusion using positron emission tomography in a phase II clinical trial of razoxane. British Journal of Cancer, 89(2), 262–267.PubMed
191.
Zurück zum Zitat Lehtio, K., et al. (2004). Imaging perfusion and hypoxia with PET to predict radiotherapy response in head-and-neck cancer. International Journal of Radiation Oncology, Biology, Physics, 59(4), 971–982.PubMed Lehtio, K., et al. (2004). Imaging perfusion and hypoxia with PET to predict radiotherapy response in head-and-neck cancer. International Journal of Radiation Oncology, Biology, Physics, 59(4), 971–982.PubMed
192.
Zurück zum Zitat Mullani, N., et al. (2000). First pass FDG measured blood flow in tumors: A comparison with O-15 labeled water measured blood flow. Clinical Positron Imaging, 3(4), 153.PubMed Mullani, N., et al. (2000). First pass FDG measured blood flow in tumors: A comparison with O-15 labeled water measured blood flow. Clinical Positron Imaging, 3(4), 153.PubMed
193.
Zurück zum Zitat Tseng, J., et al. (2004). 18F-FDG kinetics in locally advanced breast cancer: Correlation with tumor blood flow and changes in response to neoadjuvant chemotherapy. Journal of Nuclear Medicine, 45(11), 1829–1837.PubMed Tseng, J., et al. (2004). 18F-FDG kinetics in locally advanced breast cancer: Correlation with tumor blood flow and changes in response to neoadjuvant chemotherapy. Journal of Nuclear Medicine, 45(11), 1829–1837.PubMed
194.
Zurück zum Zitat Wells, P., et al. (2002). Assessment of proliferation in vivo using 2-[11C]thymidine positron emission tomography in advanced intra-abdominal malignancies. Cancer Research, 62(20), 5698–5702.PubMed Wells, P., et al. (2002). Assessment of proliferation in vivo using 2-[11C]thymidine positron emission tomography in advanced intra-abdominal malignancies. Cancer Research, 62(20), 5698–5702.PubMed
195.
Zurück zum Zitat Chen, X., et al. (2004). Pegylated Arg-Gly-Asp peptide: 64Cu labeling and PET imaging of brain tumor {alpha}v{beta}3-integrin expression. Journal of Nuclear Medicine, 45(10), 1776–1783.PubMed Chen, X., et al. (2004). Pegylated Arg-Gly-Asp peptide: 64Cu labeling and PET imaging of brain tumor {alpha}v{beta}3-integrin expression. Journal of Nuclear Medicine, 45(10), 1776–1783.PubMed
196.
Zurück zum Zitat Chen, X., et al. (2004). MicroPET imaging of breast cancer alphav-integrin expression with 64Cu-labeled dimeric RGD peptides. Molecular Imaging and Biology, 6(5), 350–359.PubMed Chen, X., et al. (2004). MicroPET imaging of breast cancer alphav-integrin expression with 64Cu-labeled dimeric RGD peptides. Molecular Imaging and Biology, 6(5), 350–359.PubMed
197.
Zurück zum Zitat Chen, X., et al. (2004). MicroPET imaging of brain tumor angiogenesis with 18F-labeled PEGylated RGD peptide. European Journal of Nuclear Medicine and Molecular Imaging, 31(8), 1081–1089.PubMed Chen, X., et al. (2004). MicroPET imaging of brain tumor angiogenesis with 18F-labeled PEGylated RGD peptide. European Journal of Nuclear Medicine and Molecular Imaging, 31(8), 1081–1089.PubMed
198.
Zurück zum Zitat Collingridge, D. R., et al. (2002). The Development of [124I]Iodinated-VG76e: A novel tracer for imaging vascular endothelial growth factor in vivo using positron emission tomography. Cancer Research, 62(20), 5912–5919.PubMed Collingridge, D. R., et al. (2002). The Development of [124I]Iodinated-VG76e: A novel tracer for imaging vascular endothelial growth factor in vivo using positron emission tomography. Cancer Research, 62(20), 5912–5919.PubMed
199.
Zurück zum Zitat Furumoto, S., et al. (2003). Tumor detection using 18F-labeled matrix metalloproteinase-2 inhibitor. Nuclear Medicine and Biology, 30(2), 119–125.PubMed Furumoto, S., et al. (2003). Tumor detection using 18F-labeled matrix metalloproteinase-2 inhibitor. Nuclear Medicine and Biology, 30(2), 119–125.PubMed
200.
Zurück zum Zitat Haubner, R., et al. (2001). Glycosylated RGD-containing peptides: Tracer for tumor targeting and angiogenesis imaging with improved biokinetics. Journal of Nuclear Medicine, 42(2), 326–336.PubMed Haubner, R., et al. (2001). Glycosylated RGD-containing peptides: Tracer for tumor targeting and angiogenesis imaging with improved biokinetics. Journal of Nuclear Medicine, 42(2), 326–336.PubMed
201.
Zurück zum Zitat Kobayashi, H., et al. (2004). Application of a macromolecular contrast agent for detection of alterations of tumor vessel permeability induced by radiation. Clinical Cancer Research, 10(22), 7712–7720.PubMed Kobayashi, H., et al. (2004). Application of a macromolecular contrast agent for detection of alterations of tumor vessel permeability induced by radiation. Clinical Cancer Research, 10(22), 7712–7720.PubMed
202.
Zurück zum Zitat Zheng, Q., et al. (2003). Synthesis, biodistribution and micro-PET imaging of a potential cancer biomarker carbon-11 labeled MMP inhibitor (2R)-2-[[4-(6-fluorohex-1-ynyl)phenyl]sulfonylamino]-3-methylbutyric acid [11C]methyl ester. Nuclear Medicine and Biology, 30(7), 753–760.PubMed Zheng, Q., et al. (2003). Synthesis, biodistribution and micro-PET imaging of a potential cancer biomarker carbon-11 labeled MMP inhibitor (2R)-2-[[4-(6-fluorohex-1-ynyl)phenyl]sulfonylamino]-3-methylbutyric acid [11C]methyl ester. Nuclear Medicine and Biology, 30(7), 753–760.PubMed
203.
Zurück zum Zitat Zinn, K., et al. (2000). Imaging Tc-99m-labeled FGF-1 targeting in rats. Nuclear Medicine and Biology, 27(4), 407–414.PubMed Zinn, K., et al. (2000). Imaging Tc-99m-labeled FGF-1 targeting in rats. Nuclear Medicine and Biology, 27(4), 407–414.PubMed
204.
Zurück zum Zitat Cai, W., et al. (2006). PET of vascular endothelial growth factor receptor expression. Journal of Nuclear Medicine, 47(12), 2048–2056.PubMed Cai, W., et al. (2006). PET of vascular endothelial growth factor receptor expression. Journal of Nuclear Medicine, 47(12), 2048–2056.PubMed
205.
Zurück zum Zitat Wang, H., et al. (2007). A new PET tracer specific for vascular endothelial growth factor receptor 2. European Journal of Nuclear Medicine and Molecular Imaging, 34(12), 2001–2010.PubMed Wang, H., et al. (2007). A new PET tracer specific for vascular endothelial growth factor receptor 2. European Journal of Nuclear Medicine and Molecular Imaging, 34(12), 2001–2010.PubMed
206.
Zurück zum Zitat Beer, A. J., et al. (2005). Biodistribution and pharmacokinetics of the {alpha}v{beta}3-selective tracer 18F-Galacto-RGD in cancer patients. Journal of Nuclear Medicine, 46(8), 1333–1341.PubMed Beer, A. J., et al. (2005). Biodistribution and pharmacokinetics of the {alpha}v{beta}3-selective tracer 18F-Galacto-RGD in cancer patients. Journal of Nuclear Medicine, 46(8), 1333–1341.PubMed
207.
Zurück zum Zitat Wu, Z., et al. (2007). MicroPET of tumor integrin {alpha}v{beta}3 expression using 18F-labeled PEGylated tetrameric RGD peptide (18F-FPRGD4). Journal of Nuclear Medicine, 48(9), 1536–1544.PubMed Wu, Z., et al. (2007). MicroPET of tumor integrin {alpha}v{beta}3 expression using 18F-labeled PEGylated tetrameric RGD peptide (18F-FPRGD4). Journal of Nuclear Medicine, 48(9), 1536–1544.PubMed
208.
Zurück zum Zitat Kamel, E., et al. (2002). CT vs 68Ge attenuation correction in a combined PET/CT system: evaluation of the effect of lowering the CT tube current. European Journal of Nuclear Medicine and Molecular Imaging, 29(3), 346–350.PubMed Kamel, E., et al. (2002). CT vs 68Ge attenuation correction in a combined PET/CT system: evaluation of the effect of lowering the CT tube current. European Journal of Nuclear Medicine and Molecular Imaging, 29(3), 346–350.PubMed
209.
Zurück zum Zitat Antoch, G., et al. (2004). Accuracy of whole-body dual-modality fluorine-18–2-Fluoro-2-Deoxy-D-Glucose Positron Emission Tomography and Computed Tomography (FDG-PET/CT) for tumor staging in solid tumors: Comparison with CT and PET. Journal of Clinical Oncology, 22(21), 4357–4368.PubMed Antoch, G., et al. (2004). Accuracy of whole-body dual-modality fluorine-18–2-Fluoro-2-Deoxy-D-Glucose Positron Emission Tomography and Computed Tomography (FDG-PET/CT) for tumor staging in solid tumors: Comparison with CT and PET. Journal of Clinical Oncology, 22(21), 4357–4368.PubMed
210.
Zurück zum Zitat Gorres, G., Steinert, H., & Schulthess, G. v. (2004). PET and functional anatomic fusion imaging in lung and breast cancers. The Cancer Journal, 10(4), 251–261.PubMed Gorres, G., Steinert, H., & Schulthess, G. v. (2004). PET and functional anatomic fusion imaging in lung and breast cancers. The Cancer Journal, 10(4), 251–261.PubMed
211.
Zurück zum Zitat Barrett, T., et al. (2007). MRI of tumor angiogenesis. Journal of Magnetic Resonance Imaging, 26(2), 235–249.PubMed Barrett, T., et al. (2007). MRI of tumor angiogenesis. Journal of Magnetic Resonance Imaging, 26(2), 235–249.PubMed
212.
Zurück zum Zitat Hylton, N. (2006). Dynamic contrast-enhanced magnetic resonance imaging as an imaging biomarker. Journal of Clinical Oncology, 24(20), 3293–3298.PubMed Hylton, N. (2006). Dynamic contrast-enhanced magnetic resonance imaging as an imaging biomarker. Journal of Clinical Oncology, 24(20), 3293–3298.PubMed
213.
Zurück zum Zitat Choyke, P., Dwyer, A., & Knopp, M. (2003). Functional tumor imaging with dynamic contrast-enhanced magnetic resonance imaging. Journal of Magnetic Resonance Imaging, 17(5), 509–520.PubMed Choyke, P., Dwyer, A., & Knopp, M. (2003). Functional tumor imaging with dynamic contrast-enhanced magnetic resonance imaging. Journal of Magnetic Resonance Imaging, 17(5), 509–520.PubMed
214.
Zurück zum Zitat Padhani, A., & Dzik-Jurasz, A. (2004). Perfusion MR imaging of extracranial tumor angiogenesis. Topics in Magnetic Resonance Imaging, 15(1), 41–57.PubMed Padhani, A., & Dzik-Jurasz, A. (2004). Perfusion MR imaging of extracranial tumor angiogenesis. Topics in Magnetic Resonance Imaging, 15(1), 41–57.PubMed
215.
Zurück zum Zitat Kiessling, F., Morgenstern, B., & Zhang, C. (2007). Contrast agents and applications to assess tumor angiogenesis in vivo by magnetic resonance imaging. Current Medicinal Chemistry, 14(1), 77–91.PubMed Kiessling, F., Morgenstern, B., & Zhang, C. (2007). Contrast agents and applications to assess tumor angiogenesis in vivo by magnetic resonance imaging. Current Medicinal Chemistry, 14(1), 77–91.PubMed
216.
Zurück zum Zitat Daldrup, H. E., et al. (1998). Quantification of the extraction fraction for gadopentetate across breast cancer capillaries. Magnetic Resonance in Medicine, 40(4), 537–543.PubMed Daldrup, H. E., et al. (1998). Quantification of the extraction fraction for gadopentetate across breast cancer capillaries. Magnetic Resonance in Medicine, 40(4), 537–543.PubMed
217.
Zurück zum Zitat Padhani, A. (2002). Dynamic contrast-enhanced MRI in clinical oncology: Current status and future directions. Journal of Magnetic Resonance Imaging, 16(4), 407–422.PubMed Padhani, A. (2002). Dynamic contrast-enhanced MRI in clinical oncology: Current status and future directions. Journal of Magnetic Resonance Imaging, 16(4), 407–422.PubMed
218.
Zurück zum Zitat Wikstrom, M., et al. (1989). Contrast-enhanced MRI of tumors. Comparison of Gd-DTPA and a macromolecular agent. Investigative Radiology, 24(8), 609–615.PubMed Wikstrom, M., et al. (1989). Contrast-enhanced MRI of tumors. Comparison of Gd-DTPA and a macromolecular agent. Investigative Radiology, 24(8), 609–615.PubMed
219.
Zurück zum Zitat Kang, H., et al. (2002). Magnetic resonance imaging of inducible E-selectin expression in human endothelial cell culture. Bioconjugate Chemistry, 13(1), 122–127.PubMed Kang, H., et al. (2002). Magnetic resonance imaging of inducible E-selectin expression in human endothelial cell culture. Bioconjugate Chemistry, 13(1), 122–127.PubMed
220.
Zurück zum Zitat McCarthy, J. R., et al. (2007). Targeted delivery of multifunctional magnetic nanoparticles. Nanomed, 2(2), 153–167.PubMed McCarthy, J. R., et al. (2007). Targeted delivery of multifunctional magnetic nanoparticles. Nanomed, 2(2), 153–167.PubMed
221.
Zurück zum Zitat Sancey, L., et al. (2007). In vivo imaging of tumour angiogenesis in mice with the alpha(v)beta (3) integrin-targeted tracer (99m)Tc-RAFT-RGD. European Journal of Nuclear Medicine and Molecular Imaging, 34, 2037–2047.PubMed Sancey, L., et al. (2007). In vivo imaging of tumour angiogenesis in mice with the alpha(v)beta (3) integrin-targeted tracer (99m)Tc-RAFT-RGD. European Journal of Nuclear Medicine and Molecular Imaging, 34, 2037–2047.PubMed
222.
Zurück zum Zitat Sipkins, D., et al. (1998). Detection of tumor angiogenesis in vivo by alphaVbeta3-targeted magnetic resonance imaging. Nature Medicine, 4(5), 623–626.PubMed Sipkins, D., et al. (1998). Detection of tumor angiogenesis in vivo by alphaVbeta3-targeted magnetic resonance imaging. Nature Medicine, 4(5), 623–626.PubMed
223.
Zurück zum Zitat Winter, P. M., et al. (2003). Molecular imaging of angiogenesis in nascent Vx-2 rabbit tumors using a novel {alpha}{nu}{beta}3-targeted nanoparticle and 1.5 tesla magnetic resonance imaging. Cancer Research, 63(18), 5838–5843.PubMed Winter, P. M., et al. (2003). Molecular imaging of angiogenesis in nascent Vx-2 rabbit tumors using a novel {alpha}{nu}{beta}3-targeted nanoparticle and 1.5 tesla magnetic resonance imaging. Cancer Research, 63(18), 5838–5843.PubMed
224.
Zurück zum Zitat Nunn, A., Linder, K., & Tweedle, M. (1997). Can receptors be imaged with MRI agents? The Quarterly Journal of Nuclear Medicine, 41(2), 155–162.PubMed Nunn, A., Linder, K., & Tweedle, M. (1997). Can receptors be imaged with MRI agents? The Quarterly Journal of Nuclear Medicine, 41(2), 155–162.PubMed
225.
Zurück zum Zitat O'Donnell, A., et al. (2005). A Phase I study of the angiogenesis inhibitor SU5416 (semaxanib) in solid tumours, incorporating dynamic contrast MR pharmacodynamic end points. British Journal of Cancer, 93(8), 876–883.PubMed O'Donnell, A., et al. (2005). A Phase I study of the angiogenesis inhibitor SU5416 (semaxanib) in solid tumours, incorporating dynamic contrast MR pharmacodynamic end points. British Journal of Cancer, 93(8), 876–883.PubMed
226.
Zurück zum Zitat Kothari, M., et al. (2003). Imaging in antiangiogenesis trial: a clinical trials radiology perspective. British Journal of Radiology, 76(suppl_1), S92–96.PubMed Kothari, M., et al. (2003). Imaging in antiangiogenesis trial: a clinical trials radiology perspective. British Journal of Radiology, 76(suppl_1), S92–96.PubMed
227.
Zurück zum Zitat Jain, R. K. (2001). Normalizing tumor vasculature with anti-angiogenic therapy: A new paradigm for combination therapy. Nature Medicine, 7(9), 987–989.PubMed Jain, R. K. (2001). Normalizing tumor vasculature with anti-angiogenic therapy: A new paradigm for combination therapy. Nature Medicine, 7(9), 987–989.PubMed
228.
Zurück zum Zitat Tatum, J. L., & Hoffman, J. M. (2000). Role of imaging in clinical trials of antiangiogenesis therapy in oncology. Academic Radiology, 7(10), 798–799.PubMed Tatum, J. L., & Hoffman, J. M. (2000). Role of imaging in clinical trials of antiangiogenesis therapy in oncology. Academic Radiology, 7(10), 798–799.PubMed
229.
Zurück zum Zitat Medved, M., et al. (2004). Semiquantitative analysis of dynamic contrast enhanced MRI in cancer patients: Variability and changes in tumor tissue over time. Journal of Magnetic Resonance Imaging, 20(1), 122–128.PubMed Medved, M., et al. (2004). Semiquantitative analysis of dynamic contrast enhanced MRI in cancer patients: Variability and changes in tumor tissue over time. Journal of Magnetic Resonance Imaging, 20(1), 122–128.PubMed
230.
Zurück zum Zitat Morgan, B., et al. (2003). Dynamic contrast-enhanced magnetic resonance imaging as a biomarker for the pharmacological response of PTK787/ZK 222584, an inhibitor of the vascular endothelial growth factor receptor tyrosine kinases, in patients with advanced colorectal cancer and liver metastases: Results from two Phase I studies. Journal of Clinical Oncology, 21(21), 3955–3964.PubMed Morgan, B., et al. (2003). Dynamic contrast-enhanced magnetic resonance imaging as a biomarker for the pharmacological response of PTK787/ZK 222584, an inhibitor of the vascular endothelial growth factor receptor tyrosine kinases, in patients with advanced colorectal cancer and liver metastases: Results from two Phase I studies. Journal of Clinical Oncology, 21(21), 3955–3964.PubMed
231.
Zurück zum Zitat Xiong, H. Q., et al. (2004). A phase I surrogate endpoint study of SU6668 in patients with solid tumors. Investigational New Drugs, 22(4), 459–466.PubMed Xiong, H. Q., et al. (2004). A phase I surrogate endpoint study of SU6668 in patients with solid tumors. Investigational New Drugs, 22(4), 459–466.PubMed
232.
Zurück zum Zitat Robinson, S. P., et al. (2007). Susceptibility contrast magnetic resonance imaging determination of fractional tumor blood volume: A noninvasive imaging biomarker of response to the vascular disrupting agent ZD6126. International Journal of Radiation Oncology, Biology, Physics, 69(3), 872–879.PubMed Robinson, S. P., et al. (2007). Susceptibility contrast magnetic resonance imaging determination of fractional tumor blood volume: A noninvasive imaging biomarker of response to the vascular disrupting agent ZD6126. International Journal of Radiation Oncology, Biology, Physics, 69(3), 872–879.PubMed
233.
Zurück zum Zitat Liu, G., et al. (2005). Dynamic contrast-enhanced magnetic resonance imaging as a pharmacodynamic measure of response after acute dosing of AG-013736, an oral angiogenesis inhibitor, in patients with advanced solid tumors: Results from a Phase I study. Journal of Clinical Oncology, 23(24), 5464–5473.PubMed Liu, G., et al. (2005). Dynamic contrast-enhanced magnetic resonance imaging as a pharmacodynamic measure of response after acute dosing of AG-013736, an oral angiogenesis inhibitor, in patients with advanced solid tumors: Results from a Phase I study. Journal of Clinical Oncology, 23(24), 5464–5473.PubMed
234.
Zurück zum Zitat Akella, N. S., et al. (2004). Assessment of brain tumor angiogenesis inhibitors using perfusion magnetic resonance imaging: Quality and analysis results of a phase I trial. Journal of Magnetic Resonance Imaging, 20(6), 913–922.PubMed Akella, N. S., et al. (2004). Assessment of brain tumor angiogenesis inhibitors using perfusion magnetic resonance imaging: Quality and analysis results of a phase I trial. Journal of Magnetic Resonance Imaging, 20(6), 913–922.PubMed
235.
Zurück zum Zitat Nabors, L. B., et al. (2007). Phase I and correlative biology study of cilengitide in patients with recurrent malignant glioma. Journal of Clinical Oncology, 25(13), 1651–1657.PubMed Nabors, L. B., et al. (2007). Phase I and correlative biology study of cilengitide in patients with recurrent malignant glioma. Journal of Clinical Oncology, 25(13), 1651–1657.PubMed
236.
Zurück zum Zitat Thomas, A. L., et al. (2005). Phase I study of the safety, tolerability, pharmacokinetics, and pharmacodynamics of PTK787/ZK 222584 administered twice daily in patients with advanced cancer. Journal of Clinical Oncology, 23(18), 4162–4171.PubMed Thomas, A. L., et al. (2005). Phase I study of the safety, tolerability, pharmacokinetics, and pharmacodynamics of PTK787/ZK 222584 administered twice daily in patients with advanced cancer. Journal of Clinical Oncology, 23(18), 4162–4171.PubMed
237.
Zurück zum Zitat Cuenod, C. A., et al. (2006). Tumor angiogenesis: Pathophysiology and implications for contrast-enhanced MRI and CT assessment. Abdominal Imaging, 31(2), 188–193.PubMed Cuenod, C. A., et al. (2006). Tumor angiogenesis: Pathophysiology and implications for contrast-enhanced MRI and CT assessment. Abdominal Imaging, 31(2), 188–193.PubMed
238.
Zurück zum Zitat Lee, T. Y., Purdie, T. G., & Stewart, E. (2003). CT imaging of angiogenesis. The Quarterly Journal of Nuclear Medicine, 47(3), 171–187.PubMed Lee, T. Y., Purdie, T. G., & Stewart, E. (2003). CT imaging of angiogenesis. The Quarterly Journal of Nuclear Medicine, 47(3), 171–187.PubMed
239.
Zurück zum Zitat Miles, K. A. (2003). Functional CT imaging in oncology. European Radiology, 13(Suppl 5), M134–M138.PubMed Miles, K. A. (2003). Functional CT imaging in oncology. European Radiology, 13(Suppl 5), M134–M138.PubMed
240.
Zurück zum Zitat Tateishi, U., et al. (2002). Contrast-enhanced dynamic computed tomography for the evaluation of tumor angiogenesis in patients with lung carcinoma. Cancer, 95(4), 835–842.PubMed Tateishi, U., et al. (2002). Contrast-enhanced dynamic computed tomography for the evaluation of tumor angiogenesis in patients with lung carcinoma. Cancer, 95(4), 835–842.PubMed
241.
Zurück zum Zitat Tateishi, U., et al. (2001). Tumor angiogenesis and dynamic CT in lung adenocarcinoma: radiologic–pathologic correlation. Journal of Computer Assisted Tomography, 25(1), 23–27.PubMed Tateishi, U., et al. (2001). Tumor angiogenesis and dynamic CT in lung adenocarcinoma: radiologic–pathologic correlation. Journal of Computer Assisted Tomography, 25(1), 23–27.PubMed
242.
Zurück zum Zitat Yi, C. A., et al. (2004). Solitary pulmonary nodules: Dynamic enhanced multi-detector row CT study and comparison with vascular endothelial growth factor and microvessel density. Radiology, 233(1), 191–199.PubMed Yi, C. A., et al. (2004). Solitary pulmonary nodules: Dynamic enhanced multi-detector row CT study and comparison with vascular endothelial growth factor and microvessel density. Radiology, 233(1), 191–199.PubMed
243.
Zurück zum Zitat Ma, S.-H., et al. (2007). Peripheral lung cancer: Relationship between multi-slice spiral CT perfusion imaging and tumor angiogenesis and cyclin D1 expression. Clinical Imaging, 31(3), 165–177.PubMed Ma, S.-H., et al. (2007). Peripheral lung cancer: Relationship between multi-slice spiral CT perfusion imaging and tumor angiogenesis and cyclin D1 expression. Clinical Imaging, 31(3), 165–177.PubMed
244.
Zurück zum Zitat Faria, S. C., et al. (2007). CT quantification of effects of thalidomide in patients with metastatic renal cell carcinoma. American Journal of Roentgenology, 189(2), 378–385.PubMed Faria, S. C., et al. (2007). CT quantification of effects of thalidomide in patients with metastatic renal cell carcinoma. American Journal of Roentgenology, 189(2), 378–385.PubMed
245.
Zurück zum Zitat McNeel, D. G., et al. (2005). Phase I trial of a monoclonal antibody specific for alphavbeta3 integrin (MEDI-522) in patients with advanced malignancies, including an assessment of effect on tumor perfusion. Clinical Cancer Research, 11(21), 7851–7860.PubMed McNeel, D. G., et al. (2005). Phase I trial of a monoclonal antibody specific for alphavbeta3 integrin (MEDI-522) in patients with advanced malignancies, including an assessment of effect on tumor perfusion. Clinical Cancer Research, 11(21), 7851–7860.PubMed
246.
Zurück zum Zitat Ng, Q.-S., et al. (2007). Effect of nitric-oxide synthesis on tumour blood volume and vascular activity: A phase I study. The Lancet Oncology, 8(2), 111–118.PubMed Ng, Q.-S., et al. (2007). Effect of nitric-oxide synthesis on tumour blood volume and vascular activity: A phase I study. The Lancet Oncology, 8(2), 111–118.PubMed
247.
Zurück zum Zitat Xiong, H. Q., et al. (2004). A phase I surrogate endpoint study of SU6668 in patients with solid tumors. Investigational New Drugs, 22(4), 459–466.PubMed Xiong, H. Q., et al. (2004). A phase I surrogate endpoint study of SU6668 in patients with solid tumors. Investigational New Drugs, 22(4), 459–466.PubMed
248.
Zurück zum Zitat Kim, J., et al. (2004). Solitary pulmonary nodules: A comparative study evaluated with contrast-enhanced dynamic MR imaging and CT. Journal of Computer Assisted Tomography, 28(6), 766–775.PubMed Kim, J., et al. (2004). Solitary pulmonary nodules: A comparative study evaluated with contrast-enhanced dynamic MR imaging and CT. Journal of Computer Assisted Tomography, 28(6), 766–775.PubMed
249.
Zurück zum Zitat Korst, R., & Altorki, N. (2004). Imaging for esophageal tumors. Thoracic Surgery Clinics, 14(1), 61–69.PubMed Korst, R., & Altorki, N. (2004). Imaging for esophageal tumors. Thoracic Surgery Clinics, 14(1), 61–69.PubMed
250.
Zurück zum Zitat Kramer, H., et al. (2004). Oesophageal endoscopic ultrasound with fine needle aspiration improves and simplifies the staging of lung cancer. Thorax, 59(7), 596–601.PubMed Kramer, H., et al. (2004). Oesophageal endoscopic ultrasound with fine needle aspiration improves and simplifies the staging of lung cancer. Thorax, 59(7), 596–601.PubMed
251.
Zurück zum Zitat Massari, M., et al. (1998). Value and limits of endorectal ultrasonography for preoperative staging of rectal carcinoma. Surgical Laparoscopy & Endoscopy, 8(6), 438–444. Massari, M., et al. (1998). Value and limits of endorectal ultrasonography for preoperative staging of rectal carcinoma. Surgical Laparoscopy & Endoscopy, 8(6), 438–444.
252.
Zurück zum Zitat Saga, Y., et al. (2004). Comparative study of novel endoluminal ultrasonography and conventional transurethral ultrasonography in staging of bladder cancer. International Journal of Urology, 11(8), 597–601.PubMed Saga, Y., et al. (2004). Comparative study of novel endoluminal ultrasonography and conventional transurethral ultrasonography in staging of bladder cancer. International Journal of Urology, 11(8), 597–601.PubMed
253.
Zurück zum Zitat Tarantino, D., & Bernstein, M. (2002). Endoanal ultrasound in the staging and management of squamous-cell carcinoma of the anal canal: Potential implications of a new ultrasound staging system. Diseases of the Colon & Rectum, 45(1), 16–22. Tarantino, D., & Bernstein, M. (2002). Endoanal ultrasound in the staging and management of squamous-cell carcinoma of the anal canal: Potential implications of a new ultrasound staging system. Diseases of the Colon & Rectum, 45(1), 16–22.
254.
Zurück zum Zitat Yanai, H., et al. (2003). Prognostic value and interobserver agreement of endoscopic ultrasonography for superficial squamous cell carcinoma of the esophagus: A prospective study. International Journal of Gastrointestinal Cancer, 34(1), 1–8.PubMed Yanai, H., et al. (2003). Prognostic value and interobserver agreement of endoscopic ultrasonography for superficial squamous cell carcinoma of the esophagus: A prospective study. International Journal of Gastrointestinal Cancer, 34(1), 1–8.PubMed
255.
Zurück zum Zitat Cosgrove, D. (2003). Angiogenesis imaging—ultrasound. British Journal of Radiology, 76(suppl_1), S43–S49.PubMed Cosgrove, D. (2003). Angiogenesis imaging—ultrasound. British Journal of Radiology, 76(suppl_1), S43–S49.PubMed
256.
Zurück zum Zitat Huber, S., et al. (1994). Breast tumors: computer-assisted quantitative assessment with color Doppler US. Radiology, 192(3), 797–801.PubMed Huber, S., et al. (1994). Breast tumors: computer-assisted quantitative assessment with color Doppler US. Radiology, 192(3), 797–801.PubMed
257.
Zurück zum Zitat Fanelli, M., et al. (1999). Assessment of tumor vascularization: Immunohistochemical and non-invasive methods. The International Journal of Biological Markers, 14(4), 218–231.PubMed Fanelli, M., et al. (1999). Assessment of tumor vascularization: Immunohistochemical and non-invasive methods. The International Journal of Biological Markers, 14(4), 218–231.PubMed
258.
Zurück zum Zitat Dayton, P., et al. (2004). Ultrasonic analysis of peptide- and antibody-targeted microbubble contrast agents for molecular imaging of alphavbeta3-expressing cells. Molecular Imaging and Biology, 3(2), 125–134. Dayton, P., et al. (2004). Ultrasonic analysis of peptide- and antibody-targeted microbubble contrast agents for molecular imaging of alphavbeta3-expressing cells. Molecular Imaging and Biology, 3(2), 125–134.
259.
Zurück zum Zitat Harrer, J., et al. (2004). Perfusion imaging of high-grade gliomas: A comparison between contrast harmonic and magnetic resonance imaging. Technical note. Journal of Neurosurgery, 101(4), 700–703.PubMed Harrer, J., et al. (2004). Perfusion imaging of high-grade gliomas: A comparison between contrast harmonic and magnetic resonance imaging. Technical note. Journal of Neurosurgery, 101(4), 700–703.PubMed
260.
Zurück zum Zitat Kiessling, F., et al. (2003). Comparing dynamic parameters of tumor vascularization in nude mice revealed by magnetic resonance imaging and contrast-enhanced intermittent power Doppler sonography. Investigative Radiology, 38(8), 516–524.PubMed Kiessling, F., et al. (2003). Comparing dynamic parameters of tumor vascularization in nude mice revealed by magnetic resonance imaging and contrast-enhanced intermittent power Doppler sonography. Investigative Radiology, 38(8), 516–524.PubMed
261.
Zurück zum Zitat Abdollahi, A., et al. (2003). Combined therapy with direct and indirect angiogenesis inhibition results in enhanced antiangiogenic and antitumor effects. Cancer Research, 63(24), 8890–8898.PubMed Abdollahi, A., et al. (2003). Combined therapy with direct and indirect angiogenesis inhibition results in enhanced antiangiogenic and antitumor effects. Cancer Research, 63(24), 8890–8898.PubMed
262.
Zurück zum Zitat Forsberg, F., et al. (2004). Assessment of angiogenesis: Implications for ultrasound imaging. Ultrasonics, 42(1–9), 325–330.PubMed Forsberg, F., et al. (2004). Assessment of angiogenesis: Implications for ultrasound imaging. Ultrasonics, 42(1–9), 325–330.PubMed
263.
Zurück zum Zitat Fury, M., et al. (2007). A Phase II study of SU5416 in patients with advanced or recurrent head and neck cancers. Investigational New Drugs, 25(2), 165–172.PubMed Fury, M., et al. (2007). A Phase II study of SU5416 in patients with advanced or recurrent head and neck cancers. Investigational New Drugs, 25(2), 165–172.PubMed
264.
Zurück zum Zitat Mross, K., et al. (2005). Phase I clinical and pharmacokinetic study of PTK/ZK, a multiple VEGF receptor inhibitor, in patients with liver metastases from solid tumours. European Journal of Cancer, 41(9), 1291–1299.PubMed Mross, K., et al. (2005). Phase I clinical and pharmacokinetic study of PTK/ZK, a multiple VEGF receptor inhibitor, in patients with liver metastases from solid tumours. European Journal of Cancer, 41(9), 1291–1299.PubMed
265.
Zurück zum Zitat Mross, K., Fuxius, S., & Drevs, J. (2002). Serial measurements of pharmacokinetics, DCE-MRI, blood flow, PET and biomarkers in serum/plasma—what is a useful tool in clinical studies of anti-angiogenic drugs? International Journal of Clinical Pharmacology and Therapeutics, 40(12), 573–574.PubMed Mross, K., Fuxius, S., & Drevs, J. (2002). Serial measurements of pharmacokinetics, DCE-MRI, blood flow, PET and biomarkers in serum/plasma—what is a useful tool in clinical studies of anti-angiogenic drugs? International Journal of Clinical Pharmacology and Therapeutics, 40(12), 573–574.PubMed
266.
Zurück zum Zitat Gibson, A. P., Hebden, J. C., & Arridge, S. R. (2005). Recent advances in diffuse optical imaging. Physics in Medicine & Biology, 50(4), R1–R43. Gibson, A. P., Hebden, J. C., & Arridge, S. R. (2005). Recent advances in diffuse optical imaging. Physics in Medicine & Biology, 50(4), R1–R43.
267.
Zurück zum Zitat Cai, W., & Chen, X. (2007). Multimodality imaging of vascular endothelial growth factor and vascular endothelial growth factor receptor expression. Frontiers in Bioscience, 12, 4267–4279.PubMed Cai, W., & Chen, X. (2007). Multimodality imaging of vascular endothelial growth factor and vascular endothelial growth factor receptor expression. Frontiers in Bioscience, 12, 4267–4279.PubMed
268.
Zurück zum Zitat Chance, B., et al. (2005). Breast cancer detection based on incremental biochemical and physiological properties of breast cancers: A six-year, two-site Study1. Academic Radiology, 12(8), 925–933.PubMed Chance, B., et al. (2005). Breast cancer detection based on incremental biochemical and physiological properties of breast cancers: A six-year, two-site Study1. Academic Radiology, 12(8), 925–933.PubMed
269.
Zurück zum Zitat Zhu, Q., et al. (2005). Benign versus malignant breast masses: Optical differentiation with US-guided optical imaging reconstruction. Radiology, 237(1), 57–66.PubMed Zhu, Q., et al. (2005). Benign versus malignant breast masses: Optical differentiation with US-guided optical imaging reconstruction. Radiology, 237(1), 57–66.PubMed
270.
Zurück zum Zitat Ntziachristos, V., & Chance, B. (2001). Probing physiology and molecular function using optical imaging: applications to breast cancer. Breast Cancer Research, 3(1), 41–46.PubMed Ntziachristos, V., & Chance, B. (2001). Probing physiology and molecular function using optical imaging: applications to breast cancer. Breast Cancer Research, 3(1), 41–46.PubMed
271.
Zurück zum Zitat Escudier, B., et al. (2007). Sorafenib in advanced clear-cell renal-cell carcinoma. The New England Journal of Medicine, 356(2), 125–134.PubMed Escudier, B., et al. (2007). Sorafenib in advanced clear-cell renal-cell carcinoma. The New England Journal of Medicine, 356(2), 125–134.PubMed
272.
Zurück zum Zitat Giantonio, B. J., et al. (2007). Bevacizumab in combination with oxaliplatin, fluorouracil, and leucovorin (FOLFOX4) for previously treated metastatic colorectal cancer: Results from the Eastern Cooperative Oncology Group Study E3200. Journal of Clinical Oncology, 25(12), 1539–1544.PubMed Giantonio, B. J., et al. (2007). Bevacizumab in combination with oxaliplatin, fluorouracil, and leucovorin (FOLFOX4) for previously treated metastatic colorectal cancer: Results from the Eastern Cooperative Oncology Group Study E3200. Journal of Clinical Oncology, 25(12), 1539–1544.PubMed
273.
Zurück zum Zitat Hurwitz, H., et al. (2004). Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer. The New England Journal of Medicine, 350(23), 2335–2342.PubMed Hurwitz, H., et al. (2004). Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer. The New England Journal of Medicine, 350(23), 2335–2342.PubMed
274.
Zurück zum Zitat Sandler, A., et al. (2006). Paclitaxel–carboplatin alone or with bevacizumab for non-small-cell lung cancer. The New England Journal of Medicine, 355(24), 2542–2550.PubMed Sandler, A., et al. (2006). Paclitaxel–carboplatin alone or with bevacizumab for non-small-cell lung cancer. The New England Journal of Medicine, 355(24), 2542–2550.PubMed
275.
Zurück zum Zitat Bonner, J. A., et al. (2006). Radiotherapy plus cetuximab for squamous-cell carcinoma of the head and neck. The New England Journal of Medicine, 354(6), 567–578.PubMed Bonner, J. A., et al. (2006). Radiotherapy plus cetuximab for squamous-cell carcinoma of the head and neck. The New England Journal of Medicine, 354(6), 567–578.PubMed
276.
Zurück zum Zitat Cunningham, D., et al. (2004). Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer. The New England Journal of Medicine, 351(4), 337–345.PubMed Cunningham, D., et al. (2004). Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer. The New England Journal of Medicine, 351(4), 337–345.PubMed
277.
Zurück zum Zitat Gibson, T. B., Ranganathan, A., & Grothey, A. (2006). Randomized phase III trial results of panitumumab, a fully human anti-epidermal growth factor receptor monoclonal antibody, in metastatic colorectal cancer. Clinical Colorectal Cancer, 6(1), 29–31.PubMed Gibson, T. B., Ranganathan, A., & Grothey, A. (2006). Randomized phase III trial results of panitumumab, a fully human anti-epidermal growth factor receptor monoclonal antibody, in metastatic colorectal cancer. Clinical Colorectal Cancer, 6(1), 29–31.PubMed
278.
Zurück zum Zitat Van Cutsem, E., et al. (2007). Open-label Phase III trial of panitumumab plus best supportive care compared with best supportive care alone in patients with chemotherapy-refractory metastatic colorectal cancer. Journal of Clinical Oncology, 25(13), 1658–1664.PubMed Van Cutsem, E., et al. (2007). Open-label Phase III trial of panitumumab plus best supportive care compared with best supportive care alone in patients with chemotherapy-refractory metastatic colorectal cancer. Journal of Clinical Oncology, 25(13), 1658–1664.PubMed
279.
Zurück zum Zitat Piccart-Gebhart, M. J., et al. (2005). Trastuzumab after adjuvant chemotherapy in HER2-positive breast cancer. The New England Journal of Medicine, 353(16), 1659–1672.PubMed Piccart-Gebhart, M. J., et al. (2005). Trastuzumab after adjuvant chemotherapy in HER2-positive breast cancer. The New England Journal of Medicine, 353(16), 1659–1672.PubMed
280.
Zurück zum Zitat Moore, M. J., et al. (2007). Erlotinib plus gemcitabine compared with gemcitabine alone in patients with advanced pancreatic cancer: A Phase III trial of the National Cancer Institute of Canada Clinical Trials Group. Journal of Clinical Oncology, 25(15), 1960–1966.PubMed Moore, M. J., et al. (2007). Erlotinib plus gemcitabine compared with gemcitabine alone in patients with advanced pancreatic cancer: A Phase III trial of the National Cancer Institute of Canada Clinical Trials Group. Journal of Clinical Oncology, 25(15), 1960–1966.PubMed
281.
Zurück zum Zitat Shepherd, F. A., et al. (2005). Erlotinib in previously treated non-small-cell lung cancer. The New England Journal of Medicine, 353(2), 123–132.PubMed Shepherd, F. A., et al. (2005). Erlotinib in previously treated non-small-cell lung cancer. The New England Journal of Medicine, 353(2), 123–132.PubMed
282.
Zurück zum Zitat Thatcher, N., et al. (2005). Gefitinib plus best supportive care in previously treated patients with refractory advanced non-small-cell lung cancer: Results from a randomised, placebo-controlled, multicentre study (Iressa Survival Evaluation in Lung Cancer). Lancet, 366(9496), 1527–1537.PubMed Thatcher, N., et al. (2005). Gefitinib plus best supportive care in previously treated patients with refractory advanced non-small-cell lung cancer: Results from a randomised, placebo-controlled, multicentre study (Iressa Survival Evaluation in Lung Cancer). Lancet, 366(9496), 1527–1537.PubMed
283.
Zurück zum Zitat Dagher, R., et al. (2002). Approval summary: Imatinib mesylate in the treatment of metastatic and/or unresectable malignant gastrointestinal stromal tumors. Clinical Cancer Research, 8(10), 3034–3038.PubMed Dagher, R., et al. (2002). Approval summary: Imatinib mesylate in the treatment of metastatic and/or unresectable malignant gastrointestinal stromal tumors. Clinical Cancer Research, 8(10), 3034–3038.PubMed
284.
Zurück zum Zitat Druker, B. J., et al. (2006). Five-year follow-up of patients receiving imatinib for chronic myeloid leukemia. The New England Journal of Medicine, 355(23), 2408–2417.PubMed Druker, B. J., et al. (2006). Five-year follow-up of patients receiving imatinib for chronic myeloid leukemia. The New England Journal of Medicine, 355(23), 2408–2417.PubMed
285.
Zurück zum Zitat Geyer, C. E., et al. (2006). Lapatinib plus capecitabine for HER2-positive advanced breast cancer. The New England Journal of Medicine, 355(26), 2733–2743.PubMed Geyer, C. E., et al. (2006). Lapatinib plus capecitabine for HER2-positive advanced breast cancer. The New England Journal of Medicine, 355(26), 2733–2743.PubMed
286.
Zurück zum Zitat Casali, P. G., et al. (2006). Updated results from a phase III trial of sunitinib in GIST patients (pts) for whom imatinib (IM) therapy has failed due to resistance or intolerance. Journal of Clinical Oncology (Meeting Abstracts), 24(18_suppl), 9513. Casali, P. G., et al. (2006). Updated results from a phase III trial of sunitinib in GIST patients (pts) for whom imatinib (IM) therapy has failed due to resistance or intolerance. Journal of Clinical Oncology (Meeting Abstracts), 24(18_suppl), 9513.
287.
Zurück zum Zitat Motzer, R. J., et al. (2007). Sunitinib versus interferon alfa in metastatic renal-cell carcinoma. The New England Journal of Medicine, 356(2), 115–124.PubMed Motzer, R. J., et al. (2007). Sunitinib versus interferon alfa in metastatic renal-cell carcinoma. The New England Journal of Medicine, 356(2), 115–124.PubMed
288.
Zurück zum Zitat Orlowski, R. Z., et al. (2007). Randomized phase III study of pegylated liposomal doxorubicin plus bortezomib compared with bortezomib alone in relapsed or refractory multiple myeloma: Combination therapy improves time to progression. Journal of Clinical Oncology, 25(25), 3892–901.PubMed Orlowski, R. Z., et al. (2007). Randomized phase III study of pegylated liposomal doxorubicin plus bortezomib compared with bortezomib alone in relapsed or refractory multiple myeloma: Combination therapy improves time to progression. Journal of Clinical Oncology, 25(25), 3892–901.PubMed
289.
Zurück zum Zitat Richardson, P. G., et al. (2005). Bortezomib or high-dose dexamethasone for relapsed multiple myeloma. The New England Journal of Medicine, 352(24), 2487–2498.PubMed Richardson, P. G., et al. (2005). Bortezomib or high-dose dexamethasone for relapsed multiple myeloma. The New England Journal of Medicine, 352(24), 2487–2498.PubMed
290.
Zurück zum Zitat Guilhot, F., et al. (1997). Interferon alfa-2b combined with cytarabine versus interferon alone in chronic myelogenous leukemia. French Chronic Myeloid Leukemia Study Group. The New England Journal of Medicine, 337(4), 223–229.PubMed Guilhot, F., et al. (1997). Interferon alfa-2b combined with cytarabine versus interferon alone in chronic myelogenous leukemia. French Chronic Myeloid Leukemia Study Group. The New England Journal of Medicine, 337(4), 223–229.PubMed
291.
Zurück zum Zitat Hauschild, A., et al. (2003). Prospective randomized trial of interferon Alfa-2b and Interleukin-2 as adjuvant treatment for resected intermediate- and high-risk primary melanoma without clinically detectable node metastasis. Journal of Clinical Oncology, 21(15), 2883–2888.PubMed Hauschild, A., et al. (2003). Prospective randomized trial of interferon Alfa-2b and Interleukin-2 as adjuvant treatment for resected intermediate- and high-risk primary melanoma without clinically detectable node metastasis. Journal of Clinical Oncology, 21(15), 2883–2888.PubMed
292.
Zurück zum Zitat Hudes, G., et al. (2007). Temsirolimus, interferon alfa, or both for advanced renal-cell carcinoma. The New England Journal of Medicine, 356(22), 2271–2281.PubMed Hudes, G., et al. (2007). Temsirolimus, interferon alfa, or both for advanced renal-cell carcinoma. The New England Journal of Medicine, 356(22), 2271–2281.PubMed
293.
Zurück zum Zitat Barlogie, B., et al. (2006). Thalidomide and hematopoietic-cell transplantation for multiple myeloma. The New England Journal of Medicine, 354(10), 1021–1030.PubMed Barlogie, B., et al. (2006). Thalidomide and hematopoietic-cell transplantation for multiple myeloma. The New England Journal of Medicine, 354(10), 1021–1030.PubMed
294.
Zurück zum Zitat Weber, D. M., et al. (2006). Lenalidomide plus high-dose dexamethasone provides improved overall survival compared to high-dose dexamethasone alone for relapsed or refractory multiple myeloma (MM): Results of a North American phase III study (MM-009). Journal of Clinical Oncology (Meeting Abstracts), 24(18_suppl), 7521. Weber, D. M., et al. (2006). Lenalidomide plus high-dose dexamethasone provides improved overall survival compared to high-dose dexamethasone alone for relapsed or refractory multiple myeloma (MM): Results of a North American phase III study (MM-009). Journal of Clinical Oncology (Meeting Abstracts), 24(18_suppl), 7521.
Metadaten
Titel
Clinical biomarkers of angiogenesis inhibition
verfasst von
Aaron P. Brown
Deborah E. Citrin
Kevin A. Camphausen
Publikationsdatum
01.09.2008
Verlag
Springer US
Erschienen in
Cancer and Metastasis Reviews / Ausgabe 3/2008
Print ISSN: 0167-7659
Elektronische ISSN: 1573-7233
DOI
https://doi.org/10.1007/s10555-008-9143-x

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