Skip to main content
Erschienen in: Journal of Gastrointestinal Cancer 1/2016

01.03.2016 | Original Research

Bevacizumab in Combination with Chemotherapy for Colorectal Brain Metastasis

verfasst von: Fabian Finkelmeier, Se-Jong You, Oliver Waidmann, Robert Wolff, Stefan Zeuzem, Oliver Bähr, Jörg Trojan

Erschienen in: Journal of Gastrointestinal Cancer | Ausgabe 1/2016

Einloggen, um Zugang zu erhalten

Abstract

Background

Brain metastases are rare in patients with colorectal cancer, but the incidence is expected to rise due to prolonged survival resulting from more effective regimens including anti-EGF-receptor and anti-angiogenic antibodies. Because of the potential fear of intracranial hemorrhage, patients with colorectal brain metastases have been excluded from clinical trials involving bevacizumab or aflibercept.

Patients

Five patients with colorectal brain metastases treated with bevacizumab-containing chemotherapy regimen following either neurosurgery, radiosurgery, or whole-brain radiotherapy were identified between 2009 and 2014. The clinicopathological data and outcomes for these patients were reviewed.

Results

Mean time to disease progression concerning brain metastases was 14.8 months (range 5–25). Overall survival was 26.2 months (range 7–42 months) and overall survival since diagnosis of brain metastases was 20.6 month (7–42). Best response was a partial response in two and a stable disease in three patients. Treatment-related adverse events were mild hypertension (grade 1), diarrhea (grade 1), and fatigue (grade 1). No intracranial hemorrhage was observed.

Conclusion

Bevacizumab in combination with chemotherapy is a feasible option for palliative treatment of patients with colorectal brain metastasis with a good safety profile.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
1.
Zurück zum Zitat Ferlay J, Shin HR, et al. Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer. 2008;127(12):2893–917.CrossRef Ferlay J, Shin HR, et al. Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer. 2008;127(12):2893–917.CrossRef
2.
Zurück zum Zitat Van der Pool AE, Damhuis RA, et al. Trends in incidence, treatment and survival of patients with stage IV colorectal cancer: a population based series. Color Dis. 2012;14(1):56–61.CrossRef Van der Pool AE, Damhuis RA, et al. Trends in incidence, treatment and survival of patients with stage IV colorectal cancer: a population based series. Color Dis. 2012;14(1):56–61.CrossRef
3.
Zurück zum Zitat Kopetz S, Chang GJ, et al. Improved survival in metastatic colorectal cancer is associated with adoption of hepatic resection and improved chemotherapy. J Clin Oncol. 2009;27(22):3677–83.PubMedCentralCrossRefPubMed Kopetz S, Chang GJ, et al. Improved survival in metastatic colorectal cancer is associated with adoption of hepatic resection and improved chemotherapy. J Clin Oncol. 2009;27(22):3677–83.PubMedCentralCrossRefPubMed
4.
Zurück zum Zitat Heinemann V, Fischer von Weikersthal L, Decker T, et al. Randomized comparison of FOLFIRI plus cetuximab versus FOLFIRI plus bevacizumab as first-line treatment of KRAS wild-type metastatic colorectal cancer: German AIO study KRK-0306 (FIRE-3). J Clin Oncol. 2013;31:2013 (suppl; abstr LBA3506). Heinemann V, Fischer von Weikersthal L, Decker T, et al. Randomized comparison of FOLFIRI plus cetuximab versus FOLFIRI plus bevacizumab as first-line treatment of KRAS wild-type metastatic colorectal cancer: German AIO study KRK-0306 (FIRE-3). J Clin Oncol. 2013;31:2013 (suppl; abstr LBA3506).
5.
Zurück zum Zitat Van Cutsem E, Peeters M, Siena S, Humblet Y, Hendlisz A, et al. 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. J Clin Oncol. 2007;25(13):1658–64.CrossRefPubMed Van Cutsem E, Peeters M, Siena S, Humblet Y, Hendlisz A, et al. 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. J Clin Oncol. 2007;25(13):1658–64.CrossRefPubMed
6.
Zurück zum Zitat Van Cutsem E, Tabernero J, Lakomy R, et al. Addition of aflibercept to fluorouracil, leucovorin, and irinotecan improves survival in a phase III randomized trial in patients with metastatic colorectal cancer previously treated with an oxaliplatin-based regimen. J Clin Oncol. 2012;30:3499–506.CrossRefPubMed Van Cutsem E, Tabernero J, Lakomy R, et al. Addition of aflibercept to fluorouracil, leucovorin, and irinotecan improves survival in a phase III randomized trial in patients with metastatic colorectal cancer previously treated with an oxaliplatin-based regimen. J Clin Oncol. 2012;30:3499–506.CrossRefPubMed
7.
Zurück zum Zitat Cunningham D, Atkin W, Lenz HJ, Lynch HT, et al. Colorectal cancer. Lancet. 2010;375:1030–47.CrossRefPubMed Cunningham D, Atkin W, Lenz HJ, Lynch HT, et al. Colorectal cancer. Lancet. 2010;375:1030–47.CrossRefPubMed
8.
Zurück zum Zitat Schouten LJ, Rutten J, Huveneers HA, et al. Incidence of brain metastases in a cohort of patients with carcinoma of the breast, colon, kidney, and lung and melanoma. Cancer. 2002;94:2698–705.CrossRefPubMed Schouten LJ, Rutten J, Huveneers HA, et al. Incidence of brain metastases in a cohort of patients with carcinoma of the breast, colon, kidney, and lung and melanoma. Cancer. 2002;94:2698–705.CrossRefPubMed
9.
Zurück zum Zitat Jung M, Ahn JB, Chang JH, Suh CO, Hong S, et al. Brain metastases from colorectal carcinoma: prognostic factors and outcome. J Neuro-Oncol. 2011;101(1):49–55.CrossRef Jung M, Ahn JB, Chang JH, Suh CO, Hong S, et al. Brain metastases from colorectal carcinoma: prognostic factors and outcome. J Neuro-Oncol. 2011;101(1):49–55.CrossRef
10.
Zurück zum Zitat Ferrara N, Davis-Smyth T. The biology of vascular endothelial growth factor. Endocr Rev. 1997;18:4–25.CrossRefPubMed Ferrara N, Davis-Smyth T. The biology of vascular endothelial growth factor. Endocr Rev. 1997;18:4–25.CrossRefPubMed
11.
Zurück zum Zitat Gerber HP, Dixit V, Ferrara N, et al. Vascular endothelial growth factor induces expression of the antiapoptotic proteins Bcl-2 and A1 in vascular endothelial cells. J Biol Chem. 1998;273:13313–6.CrossRefPubMed Gerber HP, Dixit V, Ferrara N, et al. Vascular endothelial growth factor induces expression of the antiapoptotic proteins Bcl-2 and A1 in vascular endothelial cells. J Biol Chem. 1998;273:13313–6.CrossRefPubMed
12.
Zurück zum Zitat Dvorak HF, Brown LF, Detmar M, Dvorak AM, et al. Vascular permeability factor/vascular endothelial growth factor, microvascular hyperpermeability, and angiogenesis. Am J Pathol. 1995;146:1029–39.PubMedCentralPubMed Dvorak HF, Brown LF, Detmar M, Dvorak AM, et al. Vascular permeability factor/vascular endothelial growth factor, microvascular hyperpermeability, and angiogenesis. Am J Pathol. 1995;146:1029–39.PubMedCentralPubMed
13.
Zurück zum Zitat Senger DR, Galli SJ, Dvorak AM, Perruzzi CA, Harvey VS, Dvorak HF. Tumor cells secrete a vascular permeability factor that promotes accumulation of ascites fluid. Science. 1983;219:983–5.CrossRefPubMed Senger DR, Galli SJ, Dvorak AM, Perruzzi CA, Harvey VS, Dvorak HF. Tumor cells secrete a vascular permeability factor that promotes accumulation of ascites fluid. Science. 1983;219:983–5.CrossRefPubMed
14.
15.
Zurück zum Zitat Hurwitz H, Fehrenbacher L, Novotny W, et al. Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer. NEJM. 2004;350:2335–42.CrossRefPubMed Hurwitz H, Fehrenbacher L, Novotny W, et al. Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer. NEJM. 2004;350:2335–42.CrossRefPubMed
16.
Zurück zum Zitat Saltz LB, Clarke S, Diaz-Rubio E, Scheithauer A, Figer R, et al. Bevacizumab in combination with oxaliplatin-based chemotherapy as first-line therapy in metastatic colorectal cancer: a randomized phase III study. J Clin Oncol. 2008;26(12):2013–9.CrossRefPubMed Saltz LB, Clarke S, Diaz-Rubio E, Scheithauer A, Figer R, et al. Bevacizumab in combination with oxaliplatin-based chemotherapy as first-line therapy in metastatic colorectal cancer: a randomized phase III study. J Clin Oncol. 2008;26(12):2013–9.CrossRefPubMed
17.
Zurück zum Zitat Giantano BJ, Catalano PJ, Meropol NJ, O’Dwyer PJ, et al. Bevacizumab in combination with oxaliplatin, fluorouracil, and leucovorin (FOLFOX4) for previously treated metastatic colorectal cancer, results from the Eastern Cooperative Oncology Group Study E3200. J Clin Oncol. 2007;25(12):1539–44.CrossRef Giantano BJ, Catalano PJ, Meropol NJ, O’Dwyer PJ, et al. Bevacizumab in combination with oxaliplatin, fluorouracil, and leucovorin (FOLFOX4) for previously treated metastatic colorectal cancer, results from the Eastern Cooperative Oncology Group Study E3200. J Clin Oncol. 2007;25(12):1539–44.CrossRef
18.
Zurück zum Zitat Bennouna J, Sastre J, Arnold D, Österlund P, et al. Continuation of bevacizumab after first progression in metastatic colorectal cancer (ML18147): a randomised phase 3 trial. Lancet Oncol. 2013;14(1):29–37.CrossRefPubMed Bennouna J, Sastre J, Arnold D, Österlund P, et al. Continuation of bevacizumab after first progression in metastatic colorectal cancer (ML18147): a randomised phase 3 trial. Lancet Oncol. 2013;14(1):29–37.CrossRefPubMed
19.
Zurück zum Zitat Gordon MS, Margolin K, Talpaz M, et al. Phase I safety and pharmacokinetic study of recombinant human anti-vascular endothelial growth factor in patients with advanced cancer. J Clin Oncol. 2001;19:843–50.PubMed Gordon MS, Margolin K, Talpaz M, et al. Phase I safety and pharmacokinetic study of recombinant human anti-vascular endothelial growth factor in patients with advanced cancer. J Clin Oncol. 2001;19:843–50.PubMed
20.
Zurück zum Zitat Sandler A, Gray R, Perry MC, et al. Paclitaxel–carboplatin alone or with bevacizumab for non–small-cell lung cancer. NEJM. 2006;355:2542–50.CrossRefPubMed Sandler A, Gray R, Perry MC, et al. Paclitaxel–carboplatin alone or with bevacizumab for non–small-cell lung cancer. NEJM. 2006;355:2542–50.CrossRefPubMed
21.
Zurück zum Zitat Escudier B, Pluzanska A, Koralewski P, et al. Bevacizumab plus interferon alfa-2a for treatment of metastatic renal cell carcinoma: a randomised, double-blind phase III trial. Lancet. 2007;370:2103–11.CrossRefPubMed Escudier B, Pluzanska A, Koralewski P, et al. Bevacizumab plus interferon alfa-2a for treatment of metastatic renal cell carcinoma: a randomised, double-blind phase III trial. Lancet. 2007;370:2103–11.CrossRefPubMed
22.
Zurück zum Zitat Socinski MA, Langer CJ, Huang JE, et al. Safety of bevacizumab in patients with non-small-cell lung cancer and brain metastases. J Clin Oncol. 2009;27:5255–61.CrossRefPubMed Socinski MA, Langer CJ, Huang JE, et al. Safety of bevacizumab in patients with non-small-cell lung cancer and brain metastases. J Clin Oncol. 2009;27:5255–61.CrossRefPubMed
23.
Zurück zum Zitat Archer V, Reck M, Sandler AB, et al. Risk of symptomatic central nervous system (CNS) progression and secondary hemorrhage in patients with non-squamous non-small cell lung cancer (NSCLC) receiving bevacizumab (BV)-based first-line therapy. J Clin Oncol. 2008;26:15. abstr 8114. Archer V, Reck M, Sandler AB, et al. Risk of symptomatic central nervous system (CNS) progression and secondary hemorrhage in patients with non-squamous non-small cell lung cancer (NSCLC) receiving bevacizumab (BV)-based first-line therapy. J Clin Oncol. 2008;26:15. abstr 8114.
24.
Zurück zum Zitat Therasse P, Arbuck SG, et al. New guidelines to evaluate the response to treatment in solid tumors. J Natl Cancer Inst. 2000;92(3):205–16.CrossRefPubMed Therasse P, Arbuck SG, et al. New guidelines to evaluate the response to treatment in solid tumors. J Natl Cancer Inst. 2000;92(3):205–16.CrossRefPubMed
25.
Zurück zum Zitat Eisenhauer EA, Therasse P, Bogaerts J, et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer. 2009;45(2):228–47.CrossRefPubMed Eisenhauer EA, Therasse P, Bogaerts J, et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer. 2009;45(2):228–47.CrossRefPubMed
26.
Zurück zum Zitat Besse B, Lasserre SF, Compton P, Huang J, Augustus S, Rohr UP, et al. Bevacizumab safety in patients with central nervous system metastases. Clin Cancer Res. 2010;16(1):269–78.CrossRefPubMed Besse B, Lasserre SF, Compton P, Huang J, Augustus S, Rohr UP, et al. Bevacizumab safety in patients with central nervous system metastases. Clin Cancer Res. 2010;16(1):269–78.CrossRefPubMed
27.
Zurück zum Zitat Crinò L, Dansin E, Garrido P, et al. Safety and efficacy of first-line bevacizumab-based therapy in advanced non-squamous non-small-cell lung cancer (SAiL, MO19390): a phase 4 study. Lancet. 2010;11:733–40.CrossRefPubMed Crinò L, Dansin E, Garrido P, et al. Safety and efficacy of first-line bevacizumab-based therapy in advanced non-squamous non-small-cell lung cancer (SAiL, MO19390): a phase 4 study. Lancet. 2010;11:733–40.CrossRefPubMed
28.
29.
Zurück zum Zitat Besse B, Le Moulec S, Senellart H, et al. Final overall survival (OS) results of a non comparative phase II study of bevacizumab (B) plus first-line chemotherapy or second-line erlotinib (E) in nonsquamous NSCLC patients with asymptomatic untreated brain metastases (BM)(BRAIN). J Clin Oncol. 2013; 31, (suppl; abstr 8059); ASCO Anual Meeting 2013; Abstract Number: 8059. Besse B, Le Moulec S, Senellart H, et al. Final overall survival (OS) results of a non comparative phase II study of bevacizumab (B) plus first-line chemotherapy or second-line erlotinib (E) in nonsquamous NSCLC patients with asymptomatic untreated brain metastases (BM)(BRAIN). J Clin Oncol. 2013; 31, (suppl; abstr 8059); ASCO Anual Meeting 2013; Abstract Number: 8059.
30.
Zurück zum Zitat Go PH, Klaassen Z, Meadows MC, Chamberlain R, et al. Gastrointestinal cancer and brain metastasis—a rare and omnious sign. Cancer. 2011;117(16):3630–40.CrossRefPubMed Go PH, Klaassen Z, Meadows MC, Chamberlain R, et al. Gastrointestinal cancer and brain metastasis—a rare and omnious sign. Cancer. 2011;117(16):3630–40.CrossRefPubMed
31.
Zurück zum Zitat Cascino TL, Leavengood JM, Kemeny N, Posner JB. Brain metastases from colon cancer. J Neuro-Oncol. 1983;1:203–9.CrossRef Cascino TL, Leavengood JM, Kemeny N, Posner JB. Brain metastases from colon cancer. J Neuro-Oncol. 1983;1:203–9.CrossRef
32.
Zurück zum Zitat Wronski M, Arbit E. Resection of brain metastases from colorectal carcinoma in 73 patients. Cancer. 1998;85:1677–85.CrossRef Wronski M, Arbit E. Resection of brain metastases from colorectal carcinoma in 73 patients. Cancer. 1998;85:1677–85.CrossRef
33.
Zurück zum Zitat Bartelt S, Momm F, Weissenberger C, Lutterbach J, et al. Patients with brain metastases from gastrointestinal tract cancer treated with whole brain radiation therapy: prognostic factors and survival. World J Gastroenterol. 2004;10:3345–8.PubMedCentralCrossRefPubMed Bartelt S, Momm F, Weissenberger C, Lutterbach J, et al. Patients with brain metastases from gastrointestinal tract cancer treated with whole brain radiation therapy: prognostic factors and survival. World J Gastroenterol. 2004;10:3345–8.PubMedCentralCrossRefPubMed
34.
Zurück zum Zitat Farnell GF, Buckner JC, Cascino TL, O’Connell MJ, et al. Brain metastases from colorectal carcinoma. The long term survivors. Cancer. 1996;78:711–6.CrossRefPubMed Farnell GF, Buckner JC, Cascino TL, O’Connell MJ, et al. Brain metastases from colorectal carcinoma. The long term survivors. Cancer. 1996;78:711–6.CrossRefPubMed
35.
Zurück zum Zitat Hammoud MA, McCutcheon IE, Elsouki R, Schoppa D, et al. Colorectal carcinoma and brain metastasis: distribution, treatment, and survival. Ann Surg Oncol. 1996;3:453–63.CrossRefPubMed Hammoud MA, McCutcheon IE, Elsouki R, Schoppa D, et al. Colorectal carcinoma and brain metastasis: distribution, treatment, and survival. Ann Surg Oncol. 1996;3:453–63.CrossRefPubMed
36.
Zurück zum Zitat Suzuki Y, Yamaguchi T, Matsumoto H, Nakano D, et al. Prognostic factors and treatment effects in patients with curatively resected brain metastasis from colorectal cancer. Dis Colon Rectum. 2014;57(1):56–63.CrossRefPubMed Suzuki Y, Yamaguchi T, Matsumoto H, Nakano D, et al. Prognostic factors and treatment effects in patients with curatively resected brain metastasis from colorectal cancer. Dis Colon Rectum. 2014;57(1):56–63.CrossRefPubMed
37.
Zurück zum Zitat Tsao MN, Lloyd N, Wong RK, Chow E, Rakovitch E, Laperriere N. Whole brain radiotherapy for the treatment of newly diagnosed multiple brain metastases. Cochrane Database Syst Rev. 2012; 4:CD003869. doi:10.1002/14651858.CD003869.pub3. Tsao MN, Lloyd N, Wong RK, Chow E, Rakovitch E, Laperriere N. Whole brain radiotherapy for the treatment of newly diagnosed multiple brain metastases. Cochrane Database Syst Rev. 2012; 4:CD003869. doi:10.​1002/​14651858.​CD003869.​pub3.
38.
Zurück zum Zitat Patil CG, Pricola K, Sarmiento JM, Garg SK, Bryant A, Black Kl, et al. Whole brain radiation therapy (WBRt) alone versus WBRt and radiosurgery for the treatment of brain metastases. Cochrane Database Syst Rev. 2012; 9. Patil CG, Pricola K, Sarmiento JM, Garg SK, Bryant A, Black Kl, et al. Whole brain radiation therapy (WBRt) alone versus WBRt and radiosurgery for the treatment of brain metastases. Cochrane Database Syst Rev. 2012; 9.
39.
Zurück zum Zitat O’Neill BP, Iturria NJ, Link MJ, Pollock BE, Ballman KV, O’Fallon JR, et al. A comparison of surgical resection and stereotactic radiosurgery in the treatment of solitary brain metastases. Int J Radiat Oncol Biol Phys. 2003;55:1169–76.CrossRefPubMed O’Neill BP, Iturria NJ, Link MJ, Pollock BE, Ballman KV, O’Fallon JR, et al. A comparison of surgical resection and stereotactic radiosurgery in the treatment of solitary brain metastases. Int J Radiat Oncol Biol Phys. 2003;55:1169–76.CrossRefPubMed
40.
Zurück zum Zitat Kondziolka D, Patel A, Lunsford LD, Kassam A, Flickinger JC, et al. Stereotactic radiosurgery plus whole brain radiotherapy versus radiotherapy alone for patients with multiple brain metastases. Int J Radiat Oncol Biol Phys. 1999;45:427–34.CrossRefPubMed Kondziolka D, Patel A, Lunsford LD, Kassam A, Flickinger JC, et al. Stereotactic radiosurgery plus whole brain radiotherapy versus radiotherapy alone for patients with multiple brain metastases. Int J Radiat Oncol Biol Phys. 1999;45:427–34.CrossRefPubMed
41.
Zurück zum Zitat Poulsen NHS, Grunnet K, Sorensen M, Olsen P, et al. Bevacizumab plus irinotecan in the treatment patients with progressive recurrent malignant brain tumours. Acta Oncol. 2009;48:52–8.CrossRefPubMed Poulsen NHS, Grunnet K, Sorensen M, Olsen P, et al. Bevacizumab plus irinotecan in the treatment patients with progressive recurrent malignant brain tumours. Acta Oncol. 2009;48:52–8.CrossRefPubMed
42.
Zurück zum Zitat Vredenburg JJ, Desjardins A, Hernon JE, Dowell JM, et al. Phase II trial of bevacizumab and irinotecan in recurrent malignant glioma. Clin Cancer Res. 2007;13:1253–9.CrossRef Vredenburg JJ, Desjardins A, Hernon JE, Dowell JM, et al. Phase II trial of bevacizumab and irinotecan in recurrent malignant glioma. Clin Cancer Res. 2007;13:1253–9.CrossRef
43.
Zurück zum Zitat Friedman HS, Prados MD, Wen PY, Mikkelsen T, Schiff D, Abrey LE, et al. Bevacizumab alone and in combination with irinotecan in recurrent glioblastoma. J Clin Oncol. 2009;27(28):4733–40.CrossRefPubMed Friedman HS, Prados MD, Wen PY, Mikkelsen T, Schiff D, Abrey LE, et al. Bevacizumab alone and in combination with irinotecan in recurrent glioblastoma. J Clin Oncol. 2009;27(28):4733–40.CrossRefPubMed
44.
Zurück zum Zitat Gilbert MR, Dignam JJ, Armstrong TS, Wefel JS, Blumenthal DT, et al. A randomized trial of bevacizumab for newly diagnosed glioblastoma. NEJM. 2014;370(8):699–708.PubMedCentralCrossRefPubMed Gilbert MR, Dignam JJ, Armstrong TS, Wefel JS, Blumenthal DT, et al. A randomized trial of bevacizumab for newly diagnosed glioblastoma. NEJM. 2014;370(8):699–708.PubMedCentralCrossRefPubMed
45.
Zurück zum Zitat Chinot OL, Wick W, Mason W, Henriksson R, Saran F, et al. Bevacizumab plus radiotherapy-temozolomide for newly diagnosed glioblastoma. NEJM. 2014;370(8):709–22.CrossRefPubMed Chinot OL, Wick W, Mason W, Henriksson R, Saran F, et al. Bevacizumab plus radiotherapy-temozolomide for newly diagnosed glioblastoma. NEJM. 2014;370(8):709–22.CrossRefPubMed
46.
Zurück zum Zitat Paez-Ribes M, Allen E, Hudock J, Takeda T, Okuyama H, et al. Antiangiogenic therapy elicits malignant progression of tumors to increased local invasion and distant metastasis. Cancer Cell. 2009;15:220–31.PubMedCentralCrossRefPubMed Paez-Ribes M, Allen E, Hudock J, Takeda T, Okuyama H, et al. Antiangiogenic therapy elicits malignant progression of tumors to increased local invasion and distant metastasis. Cancer Cell. 2009;15:220–31.PubMedCentralCrossRefPubMed
Metadaten
Titel
Bevacizumab in Combination with Chemotherapy for Colorectal Brain Metastasis
verfasst von
Fabian Finkelmeier
Se-Jong You
Oliver Waidmann
Robert Wolff
Stefan Zeuzem
Oliver Bähr
Jörg Trojan
Publikationsdatum
01.03.2016
Verlag
Springer US
Erschienen in
Journal of Gastrointestinal Cancer / Ausgabe 1/2016
Print ISSN: 1941-6628
Elektronische ISSN: 1941-6636
DOI
https://doi.org/10.1007/s12029-015-9795-z

Weitere Artikel der Ausgabe 1/2016

Journal of Gastrointestinal Cancer 1/2016 Zur Ausgabe

„Überwältigende“ Evidenz für Tripeltherapie beim metastasierten Prostata-Ca.

22.05.2024 Prostatakarzinom Nachrichten

Patienten mit metastasiertem hormonsensitivem Prostatakarzinom sollten nicht mehr mit einer alleinigen Androgendeprivationstherapie (ADT) behandelt werden, mahnt ein US-Team nach Sichtung der aktuellen Datenlage. Mit einer Tripeltherapie haben die Betroffenen offenbar die besten Überlebenschancen.

So sicher sind Tattoos: Neue Daten zur Risikobewertung

22.05.2024 Melanom Nachrichten

Das größte medizinische Problem bei Tattoos bleiben allergische Reaktionen. Melanome werden dadurch offensichtlich nicht gefördert, die Farbpigmente könnten aber andere Tumoren begünstigen.

CAR-M-Zellen: Warten auf das große Fressen

22.05.2024 Onkologische Immuntherapie Nachrichten

Auch myeloide Immunzellen lassen sich mit chimären Antigenrezeptoren gegen Tumoren ausstatten. Solche CAR-Fresszell-Therapien werden jetzt für solide Tumoren entwickelt. Künftig soll dieser Prozess nicht mehr ex vivo, sondern per mRNA im Körper der Betroffenen erfolgen.

Blutdrucksenkung könnte Uterusmyome verhindern

Frauen mit unbehandelter oder neu auftretender Hypertonie haben ein deutlich erhöhtes Risiko für Uterusmyome. Eine Therapie mit Antihypertensiva geht hingegen mit einer verringerten Inzidenz der gutartigen Tumoren einher.

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.