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Erschienen in: Drugs 5/2000

01.05.2000 | Review Article

Pancreatic Cancer

A Review of Emerging Therapies

verfasst von: Dr Lawrence Rosenberg

Erschienen in: Drugs | Ausgabe 5/2000

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Abstract

The incidence of adenocarcinoma of the pancreas has risen steadily over the past 4 decades. Since pancreatic cancer is diagnosed at an advanced stage, and because of the lack of effective therapies, the prognosis of such patients is extremely poor. Despite advances in our understanding of the molecular biology of pancreatic cancer, the systemic treatment of this disease remains unsatisfactory. Conventional chemotherapy has not produced dramatic improvements in response rates or patient survival. New treatment strategies are clearly needed. This paper reviews emerging therapies for pancreatic carcinoma. A more profound understanding of the molecular biology of cell growth and proliferation, as well as of neoplastic cell transformation, has led to advances in several areas, including the use of somatostatin analogues and antiandrogens as adjuvant therapy; inhibition of tumour growth and metastasis by inhibitors of matrix metalloproteinases and angiogenesis, and by small molecules such as retinoids, which interfere with progression through the cell cycle; immunotherapy with monoclonal antibodies; disruption of intracellular signal transduction with farnesyltransferase inhibitors; and finally gene therapy with specifically designed vaccines.
Literatur
1.
Zurück zum Zitat Landis S, Taylor M, Bolden S, et al. Cancer statistics, 1998. CA Cancer J Clin 1998; 48: 6–30PubMedCrossRef Landis S, Taylor M, Bolden S, et al. Cancer statistics, 1998. CA Cancer J Clin 1998; 48: 6–30PubMedCrossRef
2.
4.
Zurück zum Zitat Tsuchiya R, Noda T, Harada N, et al. Collective review of small carcinomas of the pancreas. Ann Surg 1986; 203: 77–81PubMedCrossRef Tsuchiya R, Noda T, Harada N, et al. Collective review of small carcinomas of the pancreas. Ann Surg 1986; 203: 77–81PubMedCrossRef
5.
Zurück zum Zitat DiMagno EP, Reber HA, Tempero MA. AGA technical review on the epidemiology, diagnosis and treatment of pancreatic ductal adenocarcinoma. Gastroenterology 1998; 117: 1464–84CrossRef DiMagno EP, Reber HA, Tempero MA. AGA technical review on the epidemiology, diagnosis and treatment of pancreatic ductal adenocarcinoma. Gastroenterology 1998; 117: 1464–84CrossRef
6.
Zurück zum Zitat Kelly DM, Benjamin IS. Pancreatic carcinoma. Ann Oncol 1995; 6: 19–28PubMed Kelly DM, Benjamin IS. Pancreatic carcinoma. Ann Oncol 1995; 6: 19–28PubMed
7.
8.
9.
Zurück zum Zitat Douglass H. Adjuvant therapy for pancreatic cancer. World J Surg 1995; 19: 170–4CrossRef Douglass H. Adjuvant therapy for pancreatic cancer. World J Surg 1995; 19: 170–4CrossRef
10.
Zurück zum Zitat American Cancer Society. Cancer facts and figures-1991. Atlanta (GA): American Cancer Society, 1991 American Cancer Society. Cancer facts and figures-1991. Atlanta (GA): American Cancer Society, 1991
11.
Zurück zum Zitat Connolly M, Dawson P, Michelassi F, et al. Survival in 1001 patients with carcinoma of the pancreas. Ann Surg 1987; 206: 366–73PubMedCrossRef Connolly M, Dawson P, Michelassi F, et al. Survival in 1001 patients with carcinoma of the pancreas. Ann Surg 1987; 206: 366–73PubMedCrossRef
12.
Zurück zum Zitat Singh S, Longmire W, Reber H. Surgical palliation for pancreatic cancer: The UCLA experience. Ann Surg 1990; 212: 132–9PubMedCrossRef Singh S, Longmire W, Reber H. Surgical palliation for pancreatic cancer: The UCLA experience. Ann Surg 1990; 212: 132–9PubMedCrossRef
13.
Zurück zum Zitat Ries LAG, Miller BA, Hankey BF, et al., editors. SEER cancer statistics review, 1973–1991: tables and graphs. NIH pub. no. 94-2789. Bethesda, MD: National Cancer Institute, 1994: 356–68 Ries LAG, Miller BA, Hankey BF, et al., editors. SEER cancer statistics review, 1973–1991: tables and graphs. NIH pub. no. 94-2789. Bethesda, MD: National Cancer Institute, 1994: 356–68
14.
Zurück zum Zitat Blackstock AW, Cox AD, Tepper JE. Treatment of pancreatic cancer: current limitations, future possibilities. Oncology 1996; 10: 301–30PubMed Blackstock AW, Cox AD, Tepper JE. Treatment of pancreatic cancer: current limitations, future possibilities. Oncology 1996; 10: 301–30PubMed
15.
Zurück zum Zitat Flanders TY, Foulkes WD. Pancreatic adenocarcinoma: epidemiology and genetics. J Med Genet 1996; 33: 889–98PubMedCrossRef Flanders TY, Foulkes WD. Pancreatic adenocarcinoma: epidemiology and genetics. J Med Genet 1996; 33: 889–98PubMedCrossRef
16.
Zurück zum Zitat Abruzzese JL. Pancreatic cancer: overview of current and future therapeutic approaches. Educational book of the American Society of Clinical Oncology, 33rd Annual Meeting, 1997: 65-70 Abruzzese JL. Pancreatic cancer: overview of current and future therapeutic approaches. Educational book of the American Society of Clinical Oncology, 33rd Annual Meeting, 1997: 65-70
17.
Zurück zum Zitat Rivenson A, Hoffman D, Prokopczyk B, et al. Induction of lung and exocrine pancreatic tumors in F344 rats by tobacco-specific and Areca-derived N-nitrosamines. Cancer Res 1988; 48: 6912–7PubMed Rivenson A, Hoffman D, Prokopczyk B, et al. Induction of lung and exocrine pancreatic tumors in F344 rats by tobacco-specific and Areca-derived N-nitrosamines. Cancer Res 1988; 48: 6912–7PubMed
18.
Zurück zum Zitat Pour PM, Rivenson A. Induction of a mixed ductal-squamousislet cell carcinoma in a rat treated with a tobacco-specific carcinogen. Am J Pathol 1989; 134: 627–31PubMed Pour PM, Rivenson A. Induction of a mixed ductal-squamousislet cell carcinoma in a rat treated with a tobacco-specific carcinogen. Am J Pathol 1989; 134: 627–31PubMed
19.
Zurück zum Zitat Hoffman D, Rivenson A, Chung FL, et al. Nicotine-derived N-nitrosamines (TSNA) and their relevance in tobacco carcinogenesis. Crit Rev Toxicol 1991; 21: 305–11CrossRef Hoffman D, Rivenson A, Chung FL, et al. Nicotine-derived N-nitrosamines (TSNA) and their relevance in tobacco carcinogenesis. Crit Rev Toxicol 1991; 21: 305–11CrossRef
20.
Zurück zum Zitat Ogawa T, Makino T, Mizumoto K, et al. Promoting effect of truncal vagotomy on pancreatic carcinogenesis initiated with N-nitrosobis-(2-oxopropyl) amine in Syrian golden hamsters. Carcinogenesis 1991; 12: 1227–30PubMedCrossRef Ogawa T, Makino T, Mizumoto K, et al. Promoting effect of truncal vagotomy on pancreatic carcinogenesis initiated with N-nitrosobis-(2-oxopropyl) amine in Syrian golden hamsters. Carcinogenesis 1991; 12: 1227–30PubMedCrossRef
21.
Zurück zum Zitat Corra S, Kazakoff K, Lawson TA, et al. Cholecystokinin inhibits DNA alkylation induced by N-nitrosobis (2-oxopropyl) amine (BOP) in hamster pancreas. Cancer Lett 1992; 62: 251–6PubMedCrossRef Corra S, Kazakoff K, Lawson TA, et al. Cholecystokinin inhibits DNA alkylation induced by N-nitrosobis (2-oxopropyl) amine (BOP) in hamster pancreas. Cancer Lett 1992; 62: 251–6PubMedCrossRef
22.
Zurück zum Zitat Hoffman D, Rivenson A, Abbi R, et al. A study of tobacco carcinogenesis: Effect of the fat content of the diet on the carcinogenic activity of 4 (methylnitros-amino)-1-(3-pyridyl)-1-butanone in F344 rats. Cancer Res 1993; 53: 2758–61 Hoffman D, Rivenson A, Abbi R, et al. A study of tobacco carcinogenesis: Effect of the fat content of the diet on the carcinogenic activity of 4 (methylnitros-amino)-1-(3-pyridyl)-1-butanone in F344 rats. Cancer Res 1993; 53: 2758–61
23.
Zurück zum Zitat Rosenberg L, Brown RA, Duguid WP. Development of experimental cancer in the head of the pancreas by surgical induction of tissue injury. Am J Surg 1984; 147: 146–51PubMedCrossRef Rosenberg L, Brown RA, Duguid WP. Development of experimental cancer in the head of the pancreas by surgical induction of tissue injury. Am J Surg 1984; 147: 146–51PubMedCrossRef
24.
Zurück zum Zitat Silverman DT, Dunn JA, Hoover RN, et al. Cigarette smoking and pancreas cancer: a case-control study based on direct interviews. J Natl Cancer Inst 1994; 86: 1510–6PubMedCrossRef Silverman DT, Dunn JA, Hoover RN, et al. Cigarette smoking and pancreas cancer: a case-control study based on direct interviews. J Natl Cancer Inst 1994; 86: 1510–6PubMedCrossRef
25.
Zurück zum Zitat La Vecchia C, Boyle P, Francesschi S, et al. Smoking and cancer with emphasis on Europe. Eur J Cancer 1991; 27: 94–104PubMedCrossRef La Vecchia C, Boyle P, Francesschi S, et al. Smoking and cancer with emphasis on Europe. Eur J Cancer 1991; 27: 94–104PubMedCrossRef
26.
Zurück zum Zitat Yeo C, Cameron J, Lillemoe K, et al. Pancreaticoduodenectomy for cancer of the head of the pancreas. Ann Surg 1995; 221: 721–33PubMedCrossRef Yeo C, Cameron J, Lillemoe K, et al. Pancreaticoduodenectomy for cancer of the head of the pancreas. Ann Surg 1995; 221: 721–33PubMedCrossRef
27.
Zurück zum Zitat Rothenberg ML. New developments in chemotherapy for patients with advanced pancreatic cancer. Oncology 1996; 10: 18–22PubMed Rothenberg ML. New developments in chemotherapy for patients with advanced pancreatic cancer. Oncology 1996; 10: 18–22PubMed
28.
Zurück zum Zitat Rothenberg ML, Abbruzzese JL, Moore M, et al. A rationale for expanding the endpoints for clinical trials in advanced pancreatic carcinoma. Cancer 1996; 78 (3 Suppl.): 627–32PubMed Rothenberg ML, Abbruzzese JL, Moore M, et al. A rationale for expanding the endpoints for clinical trials in advanced pancreatic carcinoma. Cancer 1996; 78 (3 Suppl.): 627–32PubMed
29.
Zurück zum Zitat Andersen JR, Friss-Mollek A, Hancke S, et al. A controlled trial of combination chemotherapy with 5-FU and BCNU in pancreatic adenocarcinoma. Scand J Gastroenterol 1981; 16: 973PubMedCrossRef Andersen JR, Friss-Mollek A, Hancke S, et al. A controlled trial of combination chemotherapy with 5-FU and BCNU in pancreatic adenocarcinoma. Scand J Gastroenterol 1981; 16: 973PubMedCrossRef
30.
Zurück zum Zitat Frey C, Twomey P, Keehn R, et al. Randomized study of 5-FU and CCNU in pancreatic cancer: report of the Veterans Administration Surgical Adjuvant Cancer Chemotherapy Study Group. Cancer 1981; 47: 27–32PubMedCrossRef Frey C, Twomey P, Keehn R, et al. Randomized study of 5-FU and CCNU in pancreatic cancer: report of the Veterans Administration Surgical Adjuvant Cancer Chemotherapy Study Group. Cancer 1981; 47: 27–32PubMedCrossRef
31.
Zurück zum Zitat Mallinson CN, Rake MO, Cocking JB, et al. Chemotherapy in pancreatic cancer: results of a controlled, prospective, randomised, multicentre trial. BMJ 1980; 281: 1589–91PubMedCrossRef Mallinson CN, Rake MO, Cocking JB, et al. Chemotherapy in pancreatic cancer: results of a controlled, prospective, randomised, multicentre trial. BMJ 1980; 281: 1589–91PubMedCrossRef
32.
Zurück zum Zitat Cullinan S, Moertel CG, Wieand HS, et al. A phase III trial on the therapy of advanced pancreatic cancer: evaluations of the Mallinson regimen and combined 5-fluorouracil, doxorubicin, and cisplatin. Cancer 1990; 65: 2207–12PubMedCrossRef Cullinan S, Moertel CG, Wieand HS, et al. A phase III trial on the therapy of advanced pancreatic cancer: evaluations of the Mallinson regimen and combined 5-fluorouracil, doxorubicin, and cisplatin. Cancer 1990; 65: 2207–12PubMedCrossRef
33.
Zurück zum Zitat Kelsen D. The use of chemotherapy in the treatment of advanced gastric and pancreatic cancer. Semin Oncol 1994; 21: 58–66PubMed Kelsen D. The use of chemotherapy in the treatment of advanced gastric and pancreatic cancer. Semin Oncol 1994; 21: 58–66PubMed
34.
Zurück zum Zitat Bukowski RM. Role of chemotherapy in patients with adenocarcinoma of the pancreas. Adv Oncol 1995; 11: 25 Bukowski RM. Role of chemotherapy in patients with adenocarcinoma of the pancreas. Adv Oncol 1995; 11: 25
35.
Zurück zum Zitat Carter SK. The integration of chemotherapy into a combined modality approach for cancer treatment. VI. Pancreatic adenocarcinoma. Cancer Treat Rev 1975; 3: 193 Carter SK. The integration of chemotherapy into a combined modality approach for cancer treatment. VI. Pancreatic adenocarcinoma. Cancer Treat Rev 1975; 3: 193
36.
Zurück zum Zitat Hubbard KP, Pazdur R, Ajani JA, et al. Phase II evaluation of iproplatin in patients with advanced gastric and pancreatic cancer. Am J Clin Oncol 1992; 15: 524–7PubMed Hubbard KP, Pazdur R, Ajani JA, et al. Phase II evaluation of iproplatin in patients with advanced gastric and pancreatic cancer. Am J Clin Oncol 1992; 15: 524–7PubMed
37.
Zurück zum Zitat Carlson RW, Doroshow JH, Odujinrin OO, et al. Trimetrexate in locally advanced or metastatic adenocarcinoma of the pancreas: a phase II study of the Northern California Oncology Group. Invest New Drugs 1990; 8: 387–9PubMedCrossRef Carlson RW, Doroshow JH, Odujinrin OO, et al. Trimetrexate in locally advanced or metastatic adenocarcinoma of the pancreas: a phase II study of the Northern California Oncology Group. Invest New Drugs 1990; 8: 387–9PubMedCrossRef
38.
Zurück zum Zitat Casper ES, Schwartz GK, Johnson B, et al. Phase II trial of edatrexate in patients with advanced pancreatic cancer. Invest New Drugs 1992; 10: 313–6PubMedCrossRef Casper ES, Schwartz GK, Johnson B, et al. Phase II trial of edatrexate in patients with advanced pancreatic cancer. Invest New Drugs 1992; 10: 313–6PubMedCrossRef
39.
Zurück zum Zitat Casper ES, Schwartz GK, Kelsen DP. Phase II trial of fazarabine (arabinofuranosyl-5-azacytidine) in patients with advanced pancreatic adenocarcinoma. Invest New Drugs 1992; 10: 205–9PubMedCrossRef Casper ES, Schwartz GK, Kelsen DP. Phase II trial of fazarabine (arabinofuranosyl-5-azacytidine) in patients with advanced pancreatic adenocarcinoma. Invest New Drugs 1992; 10: 205–9PubMedCrossRef
40.
Zurück zum Zitat Bukowski RM, Fleming TR, MacDonald JS, et al. Evaluation of combination chemotherapy and phase II agents in pancreatic adenocarcinoma: an Oncology Group study. Cancer 1993; 71: 322–5PubMedCrossRef Bukowski RM, Fleming TR, MacDonald JS, et al. Evaluation of combination chemotherapy and phase II agents in pancreatic adenocarcinoma: an Oncology Group study. Cancer 1993; 71: 322–5PubMedCrossRef
41.
Zurück zum Zitat Linke K, Pazdur R, Abbruzzese J, et al. Phase II study of amonafide in advanced pancreatic adenocarcinoma. Invest New Drugs 1991; 9: 353–6PubMedCrossRef Linke K, Pazdur R, Abbruzzese J, et al. Phase II study of amonafide in advanced pancreatic adenocarcinoma. Invest New Drugs 1991; 9: 353–6PubMedCrossRef
42.
Zurück zum Zitat Hertel LW, Boder GB, Kroin JS, et al. Evaluation of the antitumor activity of gemcitabine (2′,2′-difluoro-2′-deoxycytidine). Cancer Res 1990; 50: 4417–22PubMed Hertel LW, Boder GB, Kroin JS, et al. Evaluation of the antitumor activity of gemcitabine (2′,2′-difluoro-2′-deoxycytidine). Cancer Res 1990; 50: 4417–22PubMed
43.
Zurück zum Zitat Heinemann V, Hertel LW, Grindley GB, et al. Comparison of the cellular pharmacokinetics and toxicity of 2′,2′-difluoro-2′-deoxycytidine and 1-β-D arabinofuranosylcytosine. Cancer 1988; 48: 4024–31 Heinemann V, Hertel LW, Grindley GB, et al. Comparison of the cellular pharmacokinetics and toxicity of 2′,2′-difluoro-2′-deoxycytidine and 1-β-D arabinofuranosylcytosine. Cancer 1988; 48: 4024–31
44.
Zurück zum Zitat Abbruzzese JL, Grunewald R, Weeks EA, et al. A phase I clinical, plasma and cellular pharmacology study of gemcitabine. J Clin Oncol 1991; 9: 491–8PubMed Abbruzzese JL, Grunewald R, Weeks EA, et al. A phase I clinical, plasma and cellular pharmacology study of gemcitabine. J Clin Oncol 1991; 9: 491–8PubMed
45.
Zurück zum Zitat Casper ES, Green MR, Kelsen DP, et al. Phase II trial of gemcitabine (2′,2′-difluoro-2′-deoxycytidine) in patients with adenocarcinoma of the pancreas. Invest New Drugs 1994; 12: 29–34PubMedCrossRef Casper ES, Green MR, Kelsen DP, et al. Phase II trial of gemcitabine (2′,2′-difluoro-2′-deoxycytidine) in patients with adenocarcinoma of the pancreas. Invest New Drugs 1994; 12: 29–34PubMedCrossRef
46.
Zurück zum Zitat Burris III HA, Moore MJ, Andersen J, et al. Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: a randomized trial. J Clin Oncol 1997; 15: 2403–13PubMed Burris III HA, Moore MJ, Andersen J, et al. Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: a randomized trial. J Clin Oncol 1997; 15: 2403–13PubMed
47.
Zurück zum Zitat Rothenberg ML, Moore MJ, Cripps MC, et al. A phase II trial of gemcitabine in patients with 5-FU-refractory pancreas cancer. Ann Oncol 1996; 7: 347–53PubMedCrossRef Rothenberg ML, Moore MJ, Cripps MC, et al. A phase II trial of gemcitabine in patients with 5-FU-refractory pancreas cancer. Ann Oncol 1996; 7: 347–53PubMedCrossRef
48.
Zurück zum Zitat Gelber RD. Gemcitabine for pancreatic cancer: how hard to look for clinical benefit? An American perspective. Ann Oncol 1996; 7: 335–7PubMedCrossRef Gelber RD. Gemcitabine for pancreatic cancer: how hard to look for clinical benefit? An American perspective. Ann Oncol 1996; 7: 335–7PubMedCrossRef
49.
Zurück zum Zitat Lawrence TS, Chang EY, Hahn T, et al. Radiosensitization of pancreatic cancer cells by 2′,2′-difluoro-2′deoxycytidine. Int J Radiat Oncol Biol Phys 1996; 34: 867–72PubMedCrossRef Lawrence TS, Chang EY, Hahn T, et al. Radiosensitization of pancreatic cancer cells by 2′,2′-difluoro-2′deoxycytidine. Int J Radiat Oncol Biol Phys 1996; 34: 867–72PubMedCrossRef
50.
Zurück zum Zitat Hoffman JP, McGinn CJ, Szarka C, et al. A phase I study of preoperative gemcitabine with radiation therapy followed by postoperative gemcitabine for patients with localized, resectable pancreatic adenocarcinoma. Proc Am Soc Clin Oncol 1998; 17: 283 Hoffman JP, McGinn CJ, Szarka C, et al. A phase I study of preoperative gemcitabine with radiation therapy followed by postoperative gemcitabine for patients with localized, resectable pancreatic adenocarcinoma. Proc Am Soc Clin Oncol 1998; 17: 283
51.
Zurück zum Zitat Wolff RA, Evans DB, Gravel DM, et al. Phase I trial of gemcitabine combined with radiation for the treatment of locally advanced pancreatic adenocarcinoma. Proc Am Soc Clin Oncol 1998; 17: 283 Wolff RA, Evans DB, Gravel DM, et al. Phase I trial of gemcitabine combined with radiation for the treatment of locally advanced pancreatic adenocarcinoma. Proc Am Soc Clin Oncol 1998; 17: 283
52.
Zurück zum Zitat Abbruzzese JL, Levin B, Ajani JA, et al. A phase I trial of recombinant human interferon-gamma and recombinant human tumor necrosis factor in patients with gastrointestinal cancer. Cancer Res 1989; 49: 4057–61PubMed Abbruzzese JL, Levin B, Ajani JA, et al. A phase I trial of recombinant human interferon-gamma and recombinant human tumor necrosis factor in patients with gastrointestinal cancer. Cancer Res 1989; 49: 4057–61PubMed
53.
Zurück zum Zitat Abbruzzese JL, Levin B, Ajani JA, et al. A pilot phase II trial of recombinant human interferon-gamma and recombinant human tumor necrosis factor in patients with gastrointestinal malignancies: results of a trial terminated by excessive toxicity. J Biol Response Modif 1992; 9: 522–7 Abbruzzese JL, Levin B, Ajani JA, et al. A pilot phase II trial of recombinant human interferon-gamma and recombinant human tumor necrosis factor in patients with gastrointestinal malignancies: results of a trial terminated by excessive toxicity. J Biol Response Modif 1992; 9: 522–7
54.
Zurück zum Zitat Andren-Sanderg A, Borg S, Dawiskiba I, et al. Estrogen receptors and estrogen binding protein in pancreatic cancer. Digestion 1982; 25: 12 Andren-Sanderg A, Borg S, Dawiskiba I, et al. Estrogen receptors and estrogen binding protein in pancreatic cancer. Digestion 1982; 25: 12
55.
Zurück zum Zitat Berz C, Hollander C, Miller B. Endocrine responsive pancreatic carcinoma steroid binding and cytotoxicity studies in human tumor cell lines. Cancer Res 1986; 46: 2276–81 Berz C, Hollander C, Miller B. Endocrine responsive pancreatic carcinoma steroid binding and cytotoxicity studies in human tumor cell lines. Cancer Res 1986; 46: 2276–81
56.
Zurück zum Zitat Greenway B, Iqbal MJ, Johnson PJ, et al. Oestrogen receptor proteins in malignant and fetal pancreas. BMJ 1981; 283: 751–3PubMedCrossRef Greenway B, Iqbal MJ, Johnson PJ, et al. Oestrogen receptor proteins in malignant and fetal pancreas. BMJ 1981; 283: 751–3PubMedCrossRef
57.
Zurück zum Zitat Satake K, Yoshimoto T, Mukai R, et al. Estrogen receptors in 7,12-dimethylbenz (a) anthracene (DMBA) induced pancreatic carcinoma in rats and in human pancreatic carcinoma. Clin Oncol 1982; 8: 49–54PubMed Satake K, Yoshimoto T, Mukai R, et al. Estrogen receptors in 7,12-dimethylbenz (a) anthracene (DMBA) induced pancreatic carcinoma in rats and in human pancreatic carcinoma. Clin Oncol 1982; 8: 49–54PubMed
58.
Zurück zum Zitat Sandberg AA, Rosenthal HE. Steroid receptors in exocrine glands: the pancreas and prostate. J Steroid Biochem 1979; 11: 293–9PubMedCrossRef Sandberg AA, Rosenthal HE. Steroid receptors in exocrine glands: the pancreas and prostate. J Steroid Biochem 1979; 11: 293–9PubMedCrossRef
59.
Zurück zum Zitat Pousette A, Carlstrom K, Skoldefors H, et al. Purification and partial characterization of a 17β-estradiol-binding macromolecule in the human pancreas. Cancer Res 1982; 42: 633–7PubMed Pousette A, Carlstrom K, Skoldefors H, et al. Purification and partial characterization of a 17β-estradiol-binding macromolecule in the human pancreas. Cancer Res 1982; 42: 633–7PubMed
60.
Zurück zum Zitat Theve NO, Pousette A, Carlstrom K. Adenocarcinoma of the pancreas — a hormone sensitive tumor? A preliminary report on Nolvadex treatment. Clin Oncol 1983; 9: 193–7PubMed Theve NO, Pousette A, Carlstrom K. Adenocarcinoma of the pancreas — a hormone sensitive tumor? A preliminary report on Nolvadex treatment. Clin Oncol 1983; 9: 193–7PubMed
61.
Zurück zum Zitat Wong A, Chan A. Survival benefit of tamoxifen therapy in adenocarcinoma of pancreas.A case-control study. Cancer 1993; 71: 2200–3PubMedCrossRef Wong A, Chan A. Survival benefit of tamoxifen therapy in adenocarcinoma of pancreas.A case-control study. Cancer 1993; 71: 2200–3PubMedCrossRef
62.
63.
Zurück zum Zitat Lamberts SWJ, Krenning EP, Reubi JC. The role of somatostatin and its analogs in the diagnosis and treatment of tumors. Endocr Rev 1991; 12: 450–8PubMedCrossRef Lamberts SWJ, Krenning EP, Reubi JC. The role of somatostatin and its analogs in the diagnosis and treatment of tumors. Endocr Rev 1991; 12: 450–8PubMedCrossRef
64.
Zurück zum Zitat Arnold R, Benning R, Neuhaus R, et al. Gastroenteropancreatic endocrine tumors: effect of sandostatin on tumor growth. Digestion 1993; 54 Suppl. 1: 72–5CrossRef Arnold R, Benning R, Neuhaus R, et al. Gastroenteropancreatic endocrine tumors: effect of sandostatin on tumor growth. Digestion 1993; 54 Suppl. 1: 72–5CrossRef
65.
Zurück zum Zitat Schally AV. Oncological applications of somatostatin analogues. Cancer Res 1988; 48: 6977–85PubMed Schally AV. Oncological applications of somatostatin analogues. Cancer Res 1988; 48: 6977–85PubMed
66.
Zurück zum Zitat Johnson LR. Effects of gastrointestinal hormones on pancreatic growth. Cancer 1981; 47: 1640–5PubMedCrossRef Johnson LR. Effects of gastrointestinal hormones on pancreatic growth. Cancer 1981; 47: 1640–5PubMedCrossRef
67.
Zurück zum Zitat Comaru-Schally M, Schally AV. LH-RH agonists as adjuncts to somatostatin analogs in the treatment of pancreatic cancer. In: Lunefield B, Vickery B, editors. International symposium on Gn-RH analogues in cancer and human reproduction. Boston: Kluwer Academic Publishers, 1990: 203–10CrossRef Comaru-Schally M, Schally AV. LH-RH agonists as adjuncts to somatostatin analogs in the treatment of pancreatic cancer. In: Lunefield B, Vickery B, editors. International symposium on Gn-RH analogues in cancer and human reproduction. Boston: Kluwer Academic Publishers, 1990: 203–10CrossRef
68.
Zurück zum Zitat Konturek SJ, Bilski J, Jaworek J, et al. Comparison of somatostatin and its highly potent hexa- and octapeptide analogs on exocrine and endocrine pancreatic secretion. Proc Soc Exp Biol Med 1988; 187: 241–9PubMed Konturek SJ, Bilski J, Jaworek J, et al. Comparison of somatostatin and its highly potent hexa- and octapeptide analogs on exocrine and endocrine pancreatic secretion. Proc Soc Exp Biol Med 1988; 187: 241–9PubMed
69.
Zurück zum Zitat Stoscheck CM, King Jr LE. Role of epidermal growth factor in carcinogenesis. Cancer Res 1986; 46: 1030–7PubMed Stoscheck CM, King Jr LE. Role of epidermal growth factor in carcinogenesis. Cancer Res 1986; 46: 1030–7PubMed
70.
Zurück zum Zitat Goustin AS, Leof EB, Shipley GS, et al. Growth factors and cancer. Cancer Res 1986; 46: 1015–29PubMed Goustin AS, Leof EB, Shipley GS, et al. Growth factors and cancer. Cancer Res 1986; 46: 1015–29PubMed
71.
Zurück zum Zitat Korc M, Magnum BE. Recycling of epidermal growth factor in a human pancreatic carcinoma cell line. Proc Natl Acad Sci U S A 1985; 82: 6172–5PubMedCrossRef Korc M, Magnum BE. Recycling of epidermal growth factor in a human pancreatic carcinoma cell line. Proc Natl Acad Sci U S A 1985; 82: 6172–5PubMedCrossRef
72.
Zurück zum Zitat Lamberts SWJ, Koper JW, Reubi JC. Potential role of somatostatin analogues in the treatment of cancer. Eur J Clin Invest 1987; 17: 281–7PubMedCrossRef Lamberts SWJ, Koper JW, Reubi JC. Potential role of somatostatin analogues in the treatment of cancer. Eur J Clin Invest 1987; 17: 281–7PubMedCrossRef
73.
Zurück zum Zitat Pollak M, Constantino J, Polychronakos C, et al. Effect of tamoxifen on serum insulinlike growth factor I levels in stage 1 breast cancer patients. J Natl Cancer Inst 1990; 82: 1693–7PubMedCrossRef Pollak M, Constantino J, Polychronakos C, et al. Effect of tamoxifen on serum insulinlike growth factor I levels in stage 1 breast cancer patients. J Natl Cancer Inst 1990; 82: 1693–7PubMedCrossRef
74.
Zurück zum Zitat Pollak M, Polychronakos C, Guyda H. Somatostatin analogue SMS 201–995 reduces serum IGF levels in patients with neoplasms potentially dependent on IGF-1. Anticancer Res 1989; 9: 889–91PubMed Pollak M, Polychronakos C, Guyda H. Somatostatin analogue SMS 201–995 reduces serum IGF levels in patients with neoplasms potentially dependent on IGF-1. Anticancer Res 1989; 9: 889–91PubMed
75.
Zurück zum Zitat Huynh H, Pollak M. Enhancement of tamoxifen-induced suppression of insulin-like growth factor I gene expression and serum level by a somatostatin analogue. Biochem Biophys Res Commun 1994; 203(1): 253–9PubMedCrossRef Huynh H, Pollak M. Enhancement of tamoxifen-induced suppression of insulin-like growth factor I gene expression and serum level by a somatostatin analogue. Biochem Biophys Res Commun 1994; 203(1): 253–9PubMedCrossRef
76.
Zurück zum Zitat Poston GJ, Townsend Jr CM, Rajaraman S, et al. Effect of somatostatin and tamoxifen on the growth of human pancreatic cancers in nude mice. Pancreas 1990; 5: 151–7PubMedCrossRef Poston GJ, Townsend Jr CM, Rajaraman S, et al. Effect of somatostatin and tamoxifen on the growth of human pancreatic cancers in nude mice. Pancreas 1990; 5: 151–7PubMedCrossRef
77.
Zurück zum Zitat Klijn JGM, Hoff AM, Th AS, et al. Treatment of patients with metastatic pancreatic and gastrointestinal tumors with the somatostatin analogue Sandostatin: a phase II study including endocrine effects. Br J Cancer 1990; 62: 627–30PubMedCrossRef Klijn JGM, Hoff AM, Th AS, et al. Treatment of patients with metastatic pancreatic and gastrointestinal tumors with the somatostatin analogue Sandostatin: a phase II study including endocrine effects. Br J Cancer 1990; 62: 627–30PubMedCrossRef
78.
Zurück zum Zitat Yamada Y, Post SR, Wang K, et al. Cloning and functional characterization of a family of human and mouse somatostatin receptors expressed in brain, gastrointestinal tract, and kidney. Proc Natl Acad Sci U S A 1992; 89: 251–5PubMedCrossRef Yamada Y, Post SR, Wang K, et al. Cloning and functional characterization of a family of human and mouse somatostatin receptors expressed in brain, gastrointestinal tract, and kidney. Proc Natl Acad Sci U S A 1992; 89: 251–5PubMedCrossRef
79.
Zurück zum Zitat Yamada Y, Reisine T, Law S, et al. Somatosustin receptors, an expanding gene family cloning and functional characterization of human SSTR3, a protein coupled to adenylyl cyclase. Mol Endocrinol 1992; 6: 2136–42PubMedCrossRef Yamada Y, Reisine T, Law S, et al. Somatosustin receptors, an expanding gene family cloning and functional characterization of human SSTR3, a protein coupled to adenylyl cyclase. Mol Endocrinol 1992; 6: 2136–42PubMedCrossRef
80.
Zurück zum Zitat Xu Y, Song J, Bruno JF, et al. Molecular cloning and sequencing of a human somatostatin receptor, hSSTR4. Biochem Biophys Res Commun 1993; 193: 648–52PubMedCrossRef Xu Y, Song J, Bruno JF, et al. Molecular cloning and sequencing of a human somatostatin receptor, hSSTR4. Biochem Biophys Res Commun 1993; 193: 648–52PubMedCrossRef
81.
Zurück zum Zitat Yamada Y, Kagimoto S, Kubota A, et al. Cloning, functional expression and pharmacological characterization of a fourth (hSSTR4) and fifth (hSSThS) human somatostatin receptor subtype. Biochem Biophys Res Commun 1993; 195: 844–52PubMedCrossRef Yamada Y, Kagimoto S, Kubota A, et al. Cloning, functional expression and pharmacological characterization of a fourth (hSSTR4) and fifth (hSSThS) human somatostatin receptor subtype. Biochem Biophys Res Commun 1993; 195: 844–52PubMedCrossRef
82.
Zurück zum Zitat Bell GI, Reisine T. Molecular biology of somatostatin receptors. Trends Neurosci 1993; 16: 34–8PubMedCrossRef Bell GI, Reisine T. Molecular biology of somatostatin receptors. Trends Neurosci 1993; 16: 34–8PubMedCrossRef
83.
Zurück zum Zitat Hoyar D, Bell GI, Berelowitz M, et al. Classification and nomenclature of somatostatin receptors. Trends Pharmacol Sci 1995; 16: 86–8CrossRef Hoyar D, Bell GI, Berelowitz M, et al. Classification and nomenclature of somatostatin receptors. Trends Pharmacol Sci 1995; 16: 86–8CrossRef
84.
Zurück zum Zitat Buscail L, Delesque N, Esteve J–P, et al. Stimulation of tyrosine phosphatase and inhibition of cell proliferation by somatostatin analogues: mediation by human receptor subtypes SSTR1 and SSTR2. Proc Natl Acad Sci U S A 1994: 91: 2315–9PubMedCrossRef Buscail L, Delesque N, Esteve J–P, et al. Stimulation of tyrosine phosphatase and inhibition of cell proliferation by somatostatin analogues: mediation by human receptor subtypes SSTR1 and SSTR2. Proc Natl Acad Sci U S A 1994: 91: 2315–9PubMedCrossRef
85.
Zurück zum Zitat Buscail L, Esteve J–P, Saint-Laurent N, et al. Inhibition of cell proliferation by the somatostatin analogue RC-160 is mediated by somatostatin receptor subtypes SSTR@ and SSSTR5 through different mechanisms. Proc Natl Acad Sci U S A 1995; 92: 1580–4PubMedCrossRef Buscail L, Esteve J–P, Saint-Laurent N, et al. Inhibition of cell proliferation by the somatostatin analogue RC-160 is mediated by somatostatin receptor subtypes SSTR@ and SSSTR5 through different mechanisms. Proc Natl Acad Sci U S A 1995; 92: 1580–4PubMedCrossRef
86.
Zurück zum Zitat Raynor K, Murphy WA, Coy DH, et al. Cloned somatostatin receptors: identification of subtype selective peptides and demonstration of high affinity linear peptides. Mol Pharmacol 1993; 43: 838–44PubMed Raynor K, Murphy WA, Coy DH, et al. Cloned somatostatin receptors: identification of subtype selective peptides and demonstration of high affinity linear peptides. Mol Pharmacol 1993; 43: 838–44PubMed
87.
Zurück zum Zitat O’Carroll A–M, Raynor K, Lolait SJ, et al. Characterization of cloned human somatostatin receptor SSTR5. Mol Pharmacol 1994; 46: 291–8PubMed O’Carroll A–M, Raynor K, Lolait SJ, et al. Characterization of cloned human somatostatin receptor SSTR5. Mol Pharmacol 1994; 46: 291–8PubMed
88.
Zurück zum Zitat Patel YC, Srikant CB. Subtype selectivity of peptide analogsfor all five cloned human somatostatin receptors (hsstr 1–5). Endocrinology 1994; 135; 2814–7PubMedCrossRef Patel YC, Srikant CB. Subtype selectivity of peptide analogsfor all five cloned human somatostatin receptors (hsstr 1–5). Endocrinology 1994; 135; 2814–7PubMedCrossRef
89.
Zurück zum Zitat Upp JR, Olson D, Poison FJ, et al. Inhibition of growth of two human pancreatic adenocarcinomas in vivo by somatostatin analog SMS 201–995. Am J Surg 1988; 155: 29–35PubMedCrossRef Upp JR, Olson D, Poison FJ, et al. Inhibition of growth of two human pancreatic adenocarcinomas in vivo by somatostatin analog SMS 201–995. Am J Surg 1988; 155: 29–35PubMedCrossRef
90.
Zurück zum Zitat Liebow C, Reilly C, Serrano M, et al. Somatostatin analogs inhibit growth of pancreatic cancer by stimulating tyrosine phosphatase. Proc Natl Acad Sci U S A 1989; 86: 2003–7PubMedCrossRef Liebow C, Reilly C, Serrano M, et al. Somatostatin analogs inhibit growth of pancreatic cancer by stimulating tyrosine phosphatase. Proc Natl Acad Sci U S A 1989; 86: 2003–7PubMedCrossRef
91.
Zurück zum Zitat Fisher WE, Boros LG, O’Dorisio MS, et al. Somatostatin receptor status of pancreatic adenocarcinoma predicts response to somatostatin therapy in vitro and in vivo. Surg Forum 1995; 46: 137–40 Fisher WE, Boros LG, O’Dorisio MS, et al. Somatostatin receptor status of pancreatic adenocarcinoma predicts response to somatostatin therapy in vitro and in vivo. Surg Forum 1995; 46: 137–40
92.
Zurück zum Zitat Fisher WE, Muscarella P, O’Dorisio TP, et al. Expression of the somatostatin receptor subtype-2 gene predicts response of human pancreatic cancer to octreotide. Surgery 1996; 120: 234–40PubMedCrossRef Fisher WE, Muscarella P, O’Dorisio TP, et al. Expression of the somatostatin receptor subtype-2 gene predicts response of human pancreatic cancer to octreotide. Surgery 1996; 120: 234–40PubMedCrossRef
93.
Zurück zum Zitat Vidal C, Rauly I, Zeggari M, et al. Up-regulation of somatostatin receptors by epidermal growth factor and gastrin in pancreatic cells. Mol Pharmacol 1994; 45: 97–104 Vidal C, Rauly I, Zeggari M, et al. Up-regulation of somatostatin receptors by epidermal growth factor and gastrin in pancreatic cells. Mol Pharmacol 1994; 45: 97–104
94.
Zurück zum Zitat Lamberts SWJ, von Koetsveld P, Hofland LJ. The interrelationship between the antimitotic action of the somatostatin analog octreotide and that of cytostatic drugs and suramin. Int J Cancer 1991; 48: 938–41PubMedCrossRef Lamberts SWJ, von Koetsveld P, Hofland LJ. The interrelationship between the antimitotic action of the somatostatin analog octreotide and that of cytostatic drugs and suramin. Int J Cancer 1991; 48: 938–41PubMedCrossRef
95.
Zurück zum Zitat Weckbecker G, Raulf F, Tolcsvai L, et al. Potentiation of the anti-proliferative effects of anti-cancer drugs by octreotide in vitro and in vivo. Digestion 1996; 57 Suppl. 1: 22–8CrossRef Weckbecker G, Raulf F, Tolcsvai L, et al. Potentiation of the anti-proliferative effects of anti-cancer drugs by octreotide in vitro and in vivo. Digestion 1996; 57 Suppl. 1: 22–8CrossRef
96.
Zurück zum Zitat Radulovic S, Nagy A, Szoke B, et al. Cytotoxic analog of somatostatin containing methotrexate inhibits growth of MIA PaCa-2 human pancreatic xenografts in nude mice. Cancer Lett 1992; 62: 263–71PubMedCrossRef Radulovic S, Nagy A, Szoke B, et al. Cytotoxic analog of somatostatin containing methotrexate inhibits growth of MIA PaCa-2 human pancreatic xenografts in nude mice. Cancer Lett 1992; 62: 263–71PubMedCrossRef
97.
Zurück zum Zitat Vennin PH, Peyret JP, Bonneterre J. Effect of the long-acting somatostatin analogue SMS 201–995 in advanced breast cancer. Anticancer Res 1989; 9: 153–6PubMed Vennin PH, Peyret JP, Bonneterre J. Effect of the long-acting somatostatin analogue SMS 201–995 in advanced breast cancer. Anticancer Res 1989; 9: 153–6PubMed
98.
Zurück zum Zitat Guliana JM, Guillausseau PJ, Caron J, et al. Effects of short-term subcutaneous administration of SMS 201–995 on calcitonin plasma levels in patients suffering from medullary thyroid carcinoma. Horm Metab Res 1989; 21: 584–6PubMedCrossRef Guliana JM, Guillausseau PJ, Caron J, et al. Effects of short-term subcutaneous administration of SMS 201–995 on calcitonin plasma levels in patients suffering from medullary thyroid carcinoma. Horm Metab Res 1989; 21: 584–6PubMedCrossRef
99.
Zurück zum Zitat Kraenzlin ME, Ch’ng JC, Wood SM, et al. Long-term treatment of a VlPoma with somatostatin analogue resulting in remission of symptoms and possible shrinkage of metastases. Gastroenterology 1985; 88: 185–7PubMed Kraenzlin ME, Ch’ng JC, Wood SM, et al. Long-term treatment of a VlPoma with somatostatin analogue resulting in remission of symptoms and possible shrinkage of metastases. Gastroenterology 1985; 88: 185–7PubMed
100.
Zurück zum Zitat Parmar H, Bogden A, Mollard M, et al. Somatostatin and somatostatin analogues in oncology. Cancer Treat Rev 1989; 16: 95–115PubMedCrossRef Parmar H, Bogden A, Mollard M, et al. Somatostatin and somatostatin analogues in oncology. Cancer Treat Rev 1989; 16: 95–115PubMedCrossRef
101.
Zurück zum Zitat Morisset J, Genik P, Lord A, et al. Effects of chronic administration of somatostatin on rat exocrine pancreas. Regul Pept 1982; 4: 49–58PubMedCrossRef Morisset J, Genik P, Lord A, et al. Effects of chronic administration of somatostatin on rat exocrine pancreas. Regul Pept 1982; 4: 49–58PubMedCrossRef
102.
Zurück zum Zitat Fekete M, Zalatnai A, Comura-Schally AM, et al. Membrane receptors for peptides in experimental and human pancreatic cancers. Pancreas 1989; 4: 521–8PubMedCrossRef Fekete M, Zalatnai A, Comura-Schally AM, et al. Membrane receptors for peptides in experimental and human pancreatic cancers. Pancreas 1989; 4: 521–8PubMedCrossRef
103.
Zurück zum Zitat Davies NM, Kapur P, Gillespie J, et al. Inhibitory effect of somatostatin analog RC-160 on EGF- and transforming growth factor alpha (TGF-α)-stimulated pancreatic cancer growth in vivo. Br J Cancer 1991; 64 Suppl. 15: 4 Davies NM, Kapur P, Gillespie J, et al. Inhibitory effect of somatostatin analog RC-160 on EGF- and transforming growth factor alpha (TGF-α)-stimulated pancreatic cancer growth in vivo. Br J Cancer 1991; 64 Suppl. 15: 4
104.
Zurück zum Zitat Schally AV, Srkalovic G, Szende B, et al. Anti-tumor effects of analogs of LH-RH and somatostatin: experimental and clinical studies. J Steroid Biochem Mol Biol 1990; 37: 1061–7PubMedCrossRef Schally AV, Srkalovic G, Szende B, et al. Anti-tumor effects of analogs of LH-RH and somatostatin: experimental and clinical studies. J Steroid Biochem Mol Biol 1990; 37: 1061–7PubMedCrossRef
105.
Zurück zum Zitat Szende B, Srkalovic G, Schally AV, et al. Inhibitory effects of analogs of luteinizing hormone-releasing hormone and somatostatin on pancreatic cancers in hamsters. Cancer 1990; 65: 2279–90PubMedCrossRef Szende B, Srkalovic G, Schally AV, et al. Inhibitory effects of analogs of luteinizing hormone-releasing hormone and somatostatin on pancreatic cancers in hamsters. Cancer 1990; 65: 2279–90PubMedCrossRef
106.
Zurück zum Zitat Paz-Bouza JR, Redding TW, Schally AV. Treatment of nitrosamine-induced pancreatic tumors in hamsters with analogues of somatostatin and luteinizing hormone-releasing hormone. Proc Natl Acad Sci U S A 1987; 84: 1112–6PubMedCrossRef Paz-Bouza JR, Redding TW, Schally AV. Treatment of nitrosamine-induced pancreatic tumors in hamsters with analogues of somatostatin and luteinizing hormone-releasing hormone. Proc Natl Acad Sci U S A 1987; 84: 1112–6PubMedCrossRef
107.
108.
Zurück zum Zitat Szende B, Zalatnai A, Schally AV. Programmed cell death (apoptosis) in pancreatic cancer of hamsters after administration of analogs of luteinizing hormone releasing hormone and somatostatin. Proc Natl Acad Sci U S A 1989; 86: 1643–7PubMedCrossRef Szende B, Zalatnai A, Schally AV. Programmed cell death (apoptosis) in pancreatic cancer of hamsters after administration of analogs of luteinizing hormone releasing hormone and somatostatin. Proc Natl Acad Sci U S A 1989; 86: 1643–7PubMedCrossRef
109.
Zurück zum Zitat Klijn JGM, Setyono-Han B, Bakker GH, et al. Effects of somatostatin analog (sandostatin) treatment in experimental and human cancer. In: Klijn JGM, Paridaens R, Foekens JA, editors. Hormonal manipulation of cancer: peptides, growth factors and new (anti) steroidal agents. EORTC monograph series, Vol. 19. New York (NY): Raven Press, 1987: 459–68 Klijn JGM, Setyono-Han B, Bakker GH, et al. Effects of somatostatin analog (sandostatin) treatment in experimental and human cancer. In: Klijn JGM, Paridaens R, Foekens JA, editors. Hormonal manipulation of cancer: peptides, growth factors and new (anti) steroidal agents. EORTC monograph series, Vol. 19. New York (NY): Raven Press, 1987: 459–68
110.
Zurück zum Zitat Friess H, Buchler M, Beglinger Ch, et al. Low dose octreotide treatment is not effective in patients with advanced pancreatic cancer. Pancreas 1993; 8: 540–5PubMedCrossRef Friess H, Buchler M, Beglinger Ch, et al. Low dose octreotide treatment is not effective in patients with advanced pancreatic cancer. Pancreas 1993; 8: 540–5PubMedCrossRef
111.
Zurück zum Zitat Frieβ H, Buchler M, Ebert M, et al. Treatment of advanced pancreatic cancer with high dose octreotide. Int J Pancreatol 1993; 14: 290–1 Frieβ H, Buchler M, Ebert M, et al. Treatment of advanced pancreatic cancer with high dose octreotide. Int J Pancreatol 1993; 14: 290–1
112.
Zurück zum Zitat Ebert M, Frieβ H, Beger H, et al. Role of octreotide in the treatment of pancreatic cancer. Digestion 1994; 55 Suppl. 1: 48–51CrossRef Ebert M, Frieβ H, Beger H, et al. Role of octreotide in the treatment of pancreatic cancer. Digestion 1994; 55 Suppl. 1: 48–51CrossRef
113.
Zurück zum Zitat Scambia G, Benedetti BP, Baiochhi G, et al. Antiproliferative effects of somatostatin analog SMS 201–995 on three human breast cancer cell lines. J Cancer Res Clin Oncol 1988; 144: 106–8 Scambia G, Benedetti BP, Baiochhi G, et al. Antiproliferative effects of somatostatin analog SMS 201–995 on three human breast cancer cell lines. J Cancer Res Clin Oncol 1988; 144: 106–8
114.
Zurück zum Zitat Cascinu S, Del Ferro E, Catalano G. A randomized trial of octreotide vs best supportive care only in advanced cancer patients refractory to chemotherapy. Br J Cancer 1995; 71: 97–101PubMedCrossRef Cascinu S, Del Ferro E, Catalano G. A randomized trial of octreotide vs best supportive care only in advanced cancer patients refractory to chemotherapy. Br J Cancer 1995; 71: 97–101PubMedCrossRef
115.
Zurück zum Zitat Canobbio L, Boccardo F, Cannata D, et al. Treatment of advanced pancreatic cancer with the somatostatin analogue BIM 23014. Cancer 1992; 69: 648–50PubMedCrossRef Canobbio L, Boccardo F, Cannata D, et al. Treatment of advanced pancreatic cancer with the somatostatin analogue BIM 23014. Cancer 1992; 69: 648–50PubMedCrossRef
116.
Zurück zum Zitat Huguier M, Samama G, Testart J,, et al. Treatment of adenocarcinoma of the pancreas with somatostatin and gonadoliberin (luteinizing hormone-releasing hormone). Am J Surg 1992; 164: 348–53PubMedCrossRef Huguier M, Samama G, Testart J,, et al. Treatment of adenocarcinoma of the pancreas with somatostatin and gonadoliberin (luteinizing hormone-releasing hormone). Am J Surg 1992; 164: 348–53PubMedCrossRef
117.
Zurück zum Zitat Weckbecker G, Tolcsvai L, Stolz B, et al. Somatostatin analogue octreotide enhances the antineoplastic effects of tamoxifen and ovariectomy on 7,12-dimethylbenz(a)anthracene-induced rat mammary carcinomas. Cancer Res 54: 6334-7 Weckbecker G, Tolcsvai L, Stolz B, et al. Somatostatin analogue octreotide enhances the antineoplastic effects of tamoxifen and ovariectomy on 7,12-dimethylbenz(a)anthracene-induced rat mammary carcinomas. Cancer Res 54: 6334-7
118.
Zurück zum Zitat Rosenberg L, Barkun AN, Denis MH, et al. Low-dose octreotide and tamoxifen in the treatment of adenocarcinoma of the pancreas. Cancer 1995; 75: 23–8PubMedCrossRef Rosenberg L, Barkun AN, Denis MH, et al. Low-dose octreotide and tamoxifen in the treatment of adenocarcinoma of the pancreas. Cancer 1995; 75: 23–8PubMedCrossRef
119.
Zurück zum Zitat Fazeny B, Baur M, Prohaska M, et al. Octreotide combined with goserelin in the therapy of advanced pancreatic cancer: results of a pilot study and review of the literature. J Cancer Res Clin Oncol 1997; 123: 45–52PubMedCrossRef Fazeny B, Baur M, Prohaska M, et al. Octreotide combined with goserelin in the therapy of advanced pancreatic cancer: results of a pilot study and review of the literature. J Cancer Res Clin Oncol 1997; 123: 45–52PubMedCrossRef
120.
Zurück zum Zitat Corbishley TP, Iqbal MJ, Wilkinson ML, et al. Androgen receptor in human normal and malignant pancreatic tissue and cell lines. Cancer 1986; 57: 1992–5PubMedCrossRef Corbishley TP, Iqbal MJ, Wilkinson ML, et al. Androgen receptor in human normal and malignant pancreatic tissue and cell lines. Cancer 1986; 57: 1992–5PubMedCrossRef
121.
Zurück zum Zitat Iqbal MJ, Greenway BA, Wilkinson WL, et al. Sex steroid enzymes, aromatase and 5α reductase in the pancreas: a comparison of normal adult, foetal and malignant tissue. Clin Sci 1983; 65: 71–5PubMed Iqbal MJ, Greenway BA, Wilkinson WL, et al. Sex steroid enzymes, aromatase and 5α reductase in the pancreas: a comparison of normal adult, foetal and malignant tissue. Clin Sci 1983; 65: 71–5PubMed
122.
Zurück zum Zitat Greenway BA, Duke D, Pym B, et al. The control of human pancreatic adenocarcinoma xenografts in nude mice by hormone therapy. Br J Surg 1982; 69: 595–7PubMedCrossRef Greenway BA, Duke D, Pym B, et al. The control of human pancreatic adenocarcinoma xenografts in nude mice by hormone therapy. Br J Surg 1982; 69: 595–7PubMedCrossRef
123.
Zurück zum Zitat Greenway BA. Effect of flutamide on survival in patients with pancreatic cancer: results of a prospective, randomised, double blind, placebo controlled trial. BMJ 1998; 316: 1935–8PubMedCrossRef Greenway BA. Effect of flutamide on survival in patients with pancreatic cancer: results of a prospective, randomised, double blind, placebo controlled trial. BMJ 1998; 316: 1935–8PubMedCrossRef
124.
Zurück zum Zitat Ryan DP, Fuchs C. Chemotherapy for pancreatic cancer. Adv Oncol 1998; 14: 11–9 Ryan DP, Fuchs C. Chemotherapy for pancreatic cancer. Adv Oncol 1998; 14: 11–9
125.
Zurück zum Zitat Gibbs JB, Oliff A, Kohl NE. Farnesyltransferase inhibitors: ras research yields a potential cancer therapeutic. Cell 1994; 77: 175–8PubMedCrossRef Gibbs JB, Oliff A, Kohl NE. Farnesyltransferase inhibitors: ras research yields a potential cancer therapeutic. Cell 1994; 77: 175–8PubMedCrossRef
126.
Zurück zum Zitat Kawa S, Nikaido T, Aoki Y, et al. Arotinoid mofarotene (R040-8757) up-regulates p21 and p27 during growth inhibition of pancreatic cancer cell lines. Int J Cancer 1997; 72: 906–11PubMedCrossRef Kawa S, Nikaido T, Aoki Y, et al. Arotinoid mofarotene (R040-8757) up-regulates p21 and p27 during growth inhibition of pancreatic cancer cell lines. Int J Cancer 1997; 72: 906–11PubMedCrossRef
127.
Zurück zum Zitat Joshhi US, Dergham ST, Chen YQ, et al. Inhibition of pancreatic tumour cell growth in culture by p21 WAF1 recombinant adenovirus. Pancreas 1998; 16: 107–13CrossRef Joshhi US, Dergham ST, Chen YQ, et al. Inhibition of pancreatic tumour cell growth in culture by p21 WAF1 recombinant adenovirus. Pancreas 1998; 16: 107–13CrossRef
128.
Zurück zum Zitat Dergham ST, Dugan MC, Joshi US, et al. The clinical significance of p21WAF1/CIP-1 and p53 expression in pancreatic adenocarcinoma. Cancer 1997; 80: 372–81PubMedCrossRef Dergham ST, Dugan MC, Joshi US, et al. The clinical significance of p21WAF1/CIP-1 and p53 expression in pancreatic adenocarcinoma. Cancer 1997; 80: 372–81PubMedCrossRef
129.
Zurück zum Zitat Joshi US, Dergham ST, Chen YQ, et al. Inhibition of pancreatic tumor cell growth in culture by p21WAF1 recombinant adenovirus. Pancreas 1998; 16: 107–13PubMedCrossRef Joshi US, Dergham ST, Chen YQ, et al. Inhibition of pancreatic tumor cell growth in culture by p21WAF1 recombinant adenovirus. Pancreas 1998; 16: 107–13PubMedCrossRef
130.
Zurück zum Zitat Mohammad RM, Dugan MC, Mohamed AN, et al. Establishment of human pancreatic tumor xenograft model: potential application for preclinical evaluation of novel therapeutic agents. Pancreas 1998; 16: 19–25PubMedCrossRef Mohammad RM, Dugan MC, Mohamed AN, et al. Establishment of human pancreatic tumor xenograft model: potential application for preclinical evaluation of novel therapeutic agents. Pancreas 1998; 16: 19–25PubMedCrossRef
131.
Zurück zum Zitat Lee JH, Federoff HJ, Schoeniger LO, et al. G207, modified herpes simplex virus type 1, kills human pancreatic cancer cells in vitro. J Gastrointest Surg 1999; 3: 127–33PubMedCrossRef Lee JH, Federoff HJ, Schoeniger LO, et al. G207, modified herpes simplex virus type 1, kills human pancreatic cancer cells in vitro. J Gastrointest Surg 1999; 3: 127–33PubMedCrossRef
132.
Zurück zum Zitat Mineta T, Rabkin SD, Yazaki T, et al. Attenuated multi-mutated herpes simplex virus-1 for the treatment of malignant gliomas. Nat Med 1995; 1: 938–43PubMedCrossRef Mineta T, Rabkin SD, Yazaki T, et al. Attenuated multi-mutated herpes simplex virus-1 for the treatment of malignant gliomas. Nat Med 1995; 1: 938–43PubMedCrossRef
133.
Zurück zum Zitat Yazaki T, Manz HJ, Rabkins SD, et al. Treatment of human malignant meningiomas by G207, a replication-competent multimutated herpes simplex virus 1. Cancer Res 1995; 55: 4752–6PubMed Yazaki T, Manz HJ, Rabkins SD, et al. Treatment of human malignant meningiomas by G207, a replication-competent multimutated herpes simplex virus 1. Cancer Res 1995; 55: 4752–6PubMed
134.
Zurück zum Zitat Link Jr CJ, Levy LP, McCann LZ, et al. Gene therapy for colon cancer with the herpes simplex thymidine kinase gene. J Surg Oncol 1997; 64: 289–94PubMedCrossRef Link Jr CJ, Levy LP, McCann LZ, et al. Gene therapy for colon cancer with the herpes simplex thymidine kinase gene. J Surg Oncol 1997; 64: 289–94PubMedCrossRef
135.
Zurück zum Zitat Yeo C. Pancreatic cancer: 1998 update. J Am Coll Surg 1998; 187: 429–42PubMed Yeo C. Pancreatic cancer: 1998 update. J Am Coll Surg 1998; 187: 429–42PubMed
136.
Zurück zum Zitat Clary BM, Coveney EC, Blazer DG, et al. Active immunotherapy of pancreatic cancer with tumor cells genetically engineered to secrete multiple cytokines. Surgery 1996; 120: 174–81PubMedCrossRef Clary BM, Coveney EC, Blazer DG, et al. Active immunotherapy of pancreatic cancer with tumor cells genetically engineered to secrete multiple cytokines. Surgery 1996; 120: 174–81PubMedCrossRef
137.
Zurück zum Zitat Simons JW, Jalfee EM, Weber C, et al. Bioactivity of human GM-CSF gene transduced autologous renal vaccines. Cancer Res 1997; 57: 1537–46PubMed Simons JW, Jalfee EM, Weber C, et al. Bioactivity of human GM-CSF gene transduced autologous renal vaccines. Cancer Res 1997; 57: 1537–46PubMed
138.
Zurück zum Zitat Cheson BD, Phillips PH, Sanol M. National Cancer Institute. Clinical trials. Oncology 1997; 11: 81–90 Cheson BD, Phillips PH, Sanol M. National Cancer Institute. Clinical trials. Oncology 1997; 11: 81–90
139.
Zurück zum Zitat Jaffee EM, Schutte M, Gossett J, et al. Development and characterization of cytokine-secreting pancreatic adenocarcinoma vaccine from primary tumors for use in clinical trials. Cancer J Sci Am 1998; 4: 194–203PubMed Jaffee EM, Schutte M, Gossett J, et al. Development and characterization of cytokine-secreting pancreatic adenocarcinoma vaccine from primary tumors for use in clinical trials. Cancer J Sci Am 1998; 4: 194–203PubMed
140.
Zurück zum Zitat Friess H, Gassmann M, Buchler MW. Adjuvant therapy of pancreatic cancer using monoclonal antibodies and immune response modifiers. Int J Pancreatol 1997; 11: 43–52 Friess H, Gassmann M, Buchler MW. Adjuvant therapy of pancreatic cancer using monoclonal antibodies and immune response modifiers. Int J Pancreatol 1997; 11: 43–52
141.
Zurück zum Zitat Sears HF, Steplewski Z, Herlyn D, et al. Effects of monoclonal antibody immunotherapy on patients with gastrointestinal adenocarcinoma. J Biol Resp Mod 1984; 3: 138–50 Sears HF, Steplewski Z, Herlyn D, et al. Effects of monoclonal antibody immunotherapy on patients with gastrointestinal adenocarcinoma. J Biol Resp Mod 1984; 3: 138–50
142.
Zurück zum Zitat Adams DO, Hall T, Steplewski Z, et al. Tumors undergoing regression induced by monoclonal antibodies of the IgG2a isotype contain increased numbers of macrophages activated for a distinctive form of antibodycytolysis. Proc Natl Acad Sci U S A 1984: 81: 3506–10PubMedCrossRef Adams DO, Hall T, Steplewski Z, et al. Tumors undergoing regression induced by monoclonal antibodies of the IgG2a isotype contain increased numbers of macrophages activated for a distinctive form of antibodycytolysis. Proc Natl Acad Sci U S A 1984: 81: 3506–10PubMedCrossRef
143.
Zurück zum Zitat Tempero MA, Pour PM, Uchida E, et al. Monoclonal antibody CO 17-1A and leukopheresis in immunotherapy of pancreatic cancer. Hybridoma 1986; 5 Suppl. 1: 133–8 Tempero MA, Pour PM, Uchida E, et al. Monoclonal antibody CO 17-1A and leukopheresis in immunotherapy of pancreatic cancer. Hybridoma 1986; 5 Suppl. 1: 133–8
144.
Zurück zum Zitat Sindelar WF, Maher MM, Herlyn D, et al. Trial of therapy with monoclonal antibody 17-1A in pancreatic carcinoma: preliminary results. Hybridoma 1986; 5 Suppl. 1: 125–32 Sindelar WF, Maher MM, Herlyn D, et al. Trial of therapy with monoclonal antibody 17-1A in pancreatic carcinoma: preliminary results. Hybridoma 1986; 5 Suppl. 1: 125–32
145.
Zurück zum Zitat Tempero MA, Sivinski CL, Steplewski Z, et al. Phase II trial of gamma interferon and monoclonal antibody 17-1A in pancreatic cancer: biological and clinical effects. J Clin Oncol 1990; 8: 2019–26PubMed Tempero MA, Sivinski CL, Steplewski Z, et al. Phase II trial of gamma interferon and monoclonal antibody 17-1A in pancreatic cancer: biological and clinical effects. J Clin Oncol 1990; 8: 2019–26PubMed
146.
Zurück zum Zitat Tempero MA, Haga Y, Sivinski C, et al. Immunotherapy with monoclonal antibody (MAB) in pancreatic adenocarcinoma. Int J Pancreatol 1991; 9: 125–34PubMed Tempero MA, Haga Y, Sivinski C, et al. Immunotherapy with monoclonal antibody (MAB) in pancreatic adenocarcinoma. Int J Pancreatol 1991; 9: 125–34PubMed
147.
Zurück zum Zitat Weiner LM, Haney F, Padavic-Shaller K, et al. Phase II multicenter evaluation of prolonged murine monoclonal antibody 17-1A therapy in pancreatic carcinoma. J Immunother 1993; 13: 110–6CrossRef Weiner LM, Haney F, Padavic-Shaller K, et al. Phase II multicenter evaluation of prolonged murine monoclonal antibody 17-1A therapy in pancreatic carcinoma. J Immunother 1993; 13: 110–6CrossRef
148.
Zurück zum Zitat Bosslet K, Kern HF, Kanzy FJ, et al. A monoclonal antibody with binding and inhibiting activity towards human pancreatic carcinoma cells. I: Immunohistological and immunochemical characterization of a murine monoclonal antibody selecting for well differentiated adenocarcinomas of the pancreas. Cancer Jmmunol Immunother 1986; 23: 185–91 Bosslet K, Kern HF, Kanzy FJ, et al. A monoclonal antibody with binding and inhibiting activity towards human pancreatic carcinoma cells. I: Immunohistological and immunochemical characterization of a murine monoclonal antibody selecting for well differentiated adenocarcinomas of the pancreas. Cancer Jmmunol Immunother 1986; 23: 185–91
149.
Zurück zum Zitat Kubel R, Buchler M, Baczako K, et al. Immunohistochemistry in pancreatic cancer with new monoclonal antibodies. Lang Arch Chir 1987; 371: 243–52CrossRef Kubel R, Buchler M, Baczako K, et al. Immunohistochemistry in pancreatic cancer with new monoclonal antibodies. Lang Arch Chir 1987; 371: 243–52CrossRef
150.
Zurück zum Zitat Montz R, Klapdor R, Rothe B, et al. Immunoscintigraphy and radioimmunotherapy in patients with pancreatic carcinoma. Nuklearmedizin 1986; 25: 239–44PubMed Montz R, Klapdor R, Rothe B, et al. Immunoscintigraphy and radioimmunotherapy in patients with pancreatic carcinoma. Nuklearmedizin 1986; 25: 239–44PubMed
151.
Zurück zum Zitat Kern HF, Bosslet K, Mollenhatter J, et al. Monocyte-related functions expressed in cell lines established from human pancreatic adenocarcinoma. I. Comparative analysis of endocytotic activity, lysosomal enzyme secretion, and Superoxide anion production. Pancreas 1987; 2: 212–21 Kern HF, Bosslet K, Mollenhatter J, et al. Monocyte-related functions expressed in cell lines established from human pancreatic adenocarcinoma. I. Comparative analysis of endocytotic activity, lysosomal enzyme secretion, and Superoxide anion production. Pancreas 1987; 2: 212–21
152.
Zurück zum Zitat Kern HF, Bosslet K, Sedlacek HH, et al. Monocyte-related functions expressed in cell lines established from human pancreatic adenocarcinoma. II. Inhibition of stimulated activity by monoclonal antibodies reacting with surface antigens on tumor cells. Pancreas 1988; 3: 2–10 Kern HF, Bosslet K, Sedlacek HH, et al. Monocyte-related functions expressed in cell lines established from human pancreatic adenocarcinoma. II. Inhibition of stimulated activity by monoclonal antibodies reacting with surface antigens on tumor cells. Pancreas 1988; 3: 2–10
153.
Zurück zum Zitat Klapdor R, Lander S, Bahlo M, et al. Radioimmunotherapy of xenografts of human pancreatic carcinomas intravenous and intratumoral application of 131I-labeled monoclonal antibodies. Nuklearmedizin 1986; 25: 235–8PubMed Klapdor R, Lander S, Bahlo M, et al. Radioimmunotherapy of xenografts of human pancreatic carcinomas intravenous and intratumoral application of 131I-labeled monoclonal antibodies. Nuklearmedizin 1986; 25: 235–8PubMed
154.
Zurück zum Zitat Buchler M, Kubel R, Malfertheiner P, et al. Immunotherapy of advanced pancreatic carcinoma with the monoclonal antibody BW 494. Dtsch Med Wochenschr 1988; 113: 374–80PubMedCrossRef Buchler M, Kubel R, Malfertheiner P, et al. Immunotherapy of advanced pancreatic carcinoma with the monoclonal antibody BW 494. Dtsch Med Wochenschr 1988; 113: 374–80PubMedCrossRef
155.
Zurück zum Zitat Buchler NI, Friess H, Malfertheiner P, et al. Studies of pancreatic cancer utilizing monoclonal antibodies. Int J Pancreatol 1990; 7: 151–7PubMed Buchler NI, Friess H, Malfertheiner P, et al. Studies of pancreatic cancer utilizing monoclonal antibodies. Int J Pancreatol 1990; 7: 151–7PubMed
156.
Zurück zum Zitat Buchler M, Friess H, Schultheiss KH, et al. A randomized controlled trial of adjuvant immunotherapy (murine monoclonal antibody 494i32) in resectable pancreatic cancer. Cancer 1991; 68: 1507–12PubMedCrossRef Buchler M, Friess H, Schultheiss KH, et al. A randomized controlled trial of adjuvant immunotherapy (murine monoclonal antibody 494i32) in resectable pancreatic cancer. Cancer 1991; 68: 1507–12PubMedCrossRef
157.
Zurück zum Zitat Buchler M, Kubel R, Klapdor R, et al. Immunotherapy of pancreatic cancer with monoclonal antibody BW 494: results from a multicentric phase I-II trial. In: Beger HG, Buehler M, Schulz G, et al., editors. Cancer therapy. Berlin: Springer. 1989: 3241 Buchler M, Kubel R, Klapdor R, et al. Immunotherapy of pancreatic cancer with monoclonal antibody BW 494: results from a multicentric phase I-II trial. In: Beger HG, Buehler M, Schulz G, et al., editors. Cancer therapy. Berlin: Springer. 1989: 3241
158.
Zurück zum Zitat Friess H, Buchler M, Schulz G, et al. Therapy of pancreatic carcinoma with the monoclonal antibody BW494/32: first clinical results. Immunitat Infekt 1989; 17: 2–26 Friess H, Buchler M, Schulz G, et al. Therapy of pancreatic carcinoma with the monoclonal antibody BW494/32: first clinical results. Immunitat Infekt 1989; 17: 2–26
159.
Zurück zum Zitat Bosslet K, Keweloh HC, Hermentin P, et al. Percolation and binding of monoclonal antibody BW494 to pancreatic carcinoma tissues during high dose immunotherapy and consequences for future therapy modalities. Br J Cancer 1990; 10: 37–9 Bosslet K, Keweloh HC, Hermentin P, et al. Percolation and binding of monoclonal antibody BW494 to pancreatic carcinoma tissues during high dose immunotherapy and consequences for future therapy modalities. Br J Cancer 1990; 10: 37–9
160.
Zurück zum Zitat Goodman GE, Hellstrom I, Yelton D, et al. Phase I trial of chimeric (human-mouse) monoclonal antibody L6 in patients with non-small-cell lung. colon. and breast cancer. Cancer Immunol Immunother 1993: 36: 267–73PubMedCrossRef Goodman GE, Hellstrom I, Yelton D, et al. Phase I trial of chimeric (human-mouse) monoclonal antibody L6 in patients with non-small-cell lung. colon. and breast cancer. Cancer Immunol Immunother 1993: 36: 267–73PubMedCrossRef
161.
Zurück zum Zitat Kushner BH, Cheung NK. GM-CSF enhances 3F8 monoclonal antibody-dependent cellular cytotoxicity against human melanoma and neuroblastoma. Blood 1989; 73: 1936–41PubMed Kushner BH, Cheung NK. GM-CSF enhances 3F8 monoclonal antibody-dependent cellular cytotoxicity against human melanoma and neuroblastoma. Blood 1989; 73: 1936–41PubMed
162.
Zurück zum Zitat Senter PD. Activation of prodrugs by antibody-enzyme conjugates: a new approach to cancer therapy. FASEB J 1990: 4: 188–93PubMed Senter PD. Activation of prodrugs by antibody-enzyme conjugates: a new approach to cancer therapy. FASEB J 1990: 4: 188–93PubMed
163.
Zurück zum Zitat Svensson HP, Kadow JF, Vrudhula VM, et al. Monoclonal antibody-beta-lactamase conjugates for the activation of a cephalosporin mustard prodrug. Bioconjug Chem 1992;3: 176–81PubMedCrossRef Svensson HP, Kadow JF, Vrudhula VM, et al. Monoclonal antibody-beta-lactamase conjugates for the activation of a cephalosporin mustard prodrug. Bioconjug Chem 1992;3: 176–81PubMedCrossRef
164.
Zurück zum Zitat Senter PD, Wallace PM, Svensson HP, et al. Activation of prodrugs by antibody-enzyme conjugates. Adv Exp Med Biol 1991; 303: 97–105PubMedCrossRef Senter PD, Wallace PM, Svensson HP, et al. Activation of prodrugs by antibody-enzyme conjugates. Adv Exp Med Biol 1991; 303: 97–105PubMedCrossRef
165.
Zurück zum Zitat Stalb F, Link KH, Mitchell MS. Immunomodulation of pancreatic cancer in vitro. Effect of monoclonal antibodies, GM-CSF and lymphokine-activated killer cells. Digestion 1992: 52: 124 Stalb F, Link KH, Mitchell MS. Immunomodulation of pancreatic cancer in vitro. Effect of monoclonal antibodies, GM-CSF and lymphokine-activated killer cells. Digestion 1992: 52: 124
166.
Zurück zum Zitat Butera J, Malachovsky M, Rathore R, et al. Novel approaches in development for the treatment of pancreatic cancer. Front Biosci 1998; 3: E226–9PubMed Butera J, Malachovsky M, Rathore R, et al. Novel approaches in development for the treatment of pancreatic cancer. Front Biosci 1998; 3: E226–9PubMed
167.
Zurück zum Zitat Nagakawa T, Konishi I, Higashino Y, et al. The spread and prognosis of carcinoma in the region of the pancreatic head. Jpn J Surg 1989; 19: 510–8PubMedCrossRef Nagakawa T, Konishi I, Higashino Y, et al. The spread and prognosis of carcinoma in the region of the pancreatic head. Jpn J Surg 1989; 19: 510–8PubMedCrossRef
168.
Zurück zum Zitat Nagakawa T, Kavahara M, Ueno K, et al. A clinicopathologic study on neural invasion in cancer of the pancreatic bead. Cancer 1992; 69: 930–5PubMedCrossRef Nagakawa T, Kavahara M, Ueno K, et al. A clinicopathologic study on neural invasion in cancer of the pancreatic bead. Cancer 1992; 69: 930–5PubMedCrossRef
169.
Zurück zum Zitat Mollenhauer J, Roether 1, Kern HF. Distribution of extracellular matrix proteins in pancreatic ductal adenocarcinoma and its influence on tumor cell proliferation in vitro. Pancreas 1987; 2: 14–24PubMedCrossRef Mollenhauer J, Roether 1, Kern HF. Distribution of extracellular matrix proteins in pancreatic ductal adenocarcinoma and its influence on tumor cell proliferation in vitro. Pancreas 1987; 2: 14–24PubMedCrossRef
170.
Zurück zum Zitat Bramhall SR. The matrix metalloproteinases and their inhibitors in pancreatic cancer. Int J Pancreatol 1997; 21: 1–12PubMed Bramhall SR. The matrix metalloproteinases and their inhibitors in pancreatic cancer. Int J Pancreatol 1997; 21: 1–12PubMed
171.
Zurück zum Zitat Hart IR, Goode NT, Wilson RE. Molecular aspects of the metastatic cascade. Biochem Biophys Acta 1989; 989: 65–84PubMed Hart IR, Goode NT, Wilson RE. Molecular aspects of the metastatic cascade. Biochem Biophys Acta 1989; 989: 65–84PubMed
172.
Zurück zum Zitat Liotta LA, Tryggvason K, Garbisa S, et al. Metastatic potential correlates with enzymatic degradation of basement membrane collagen. Nature 1980; 284: 67–8PubMedCrossRef Liotta LA, Tryggvason K, Garbisa S, et al. Metastatic potential correlates with enzymatic degradation of basement membrane collagen. Nature 1980; 284: 67–8PubMedCrossRef
173.
Zurück zum Zitat Liotta LA, Stetler-Stevenson WG. Tumor invasion and metastasis: an imbalance of positive and negative regulation. Cancer Res 1991; 51 Suppl.: 5054–9s Liotta LA, Stetler-Stevenson WG. Tumor invasion and metastasis: an imbalance of positive and negative regulation. Cancer Res 1991; 51 Suppl.: 5054–9s
174.
Zurück zum Zitat Martinez-Hernandez A, Amenta PS. The basement membrane in pathology. Lab Invest 1983; 48: 650–77 Martinez-Hernandez A, Amenta PS. The basement membrane in pathology. Lab Invest 1983; 48: 650–77
175.
Zurück zum Zitat Forster SJ, Talbot IC, Clayton DG, et al. Tumour basement membrane laminin in adenocarcinoma of rectum: an immuno-histochemical study of biological andclinical significance. Int J Cancer 1986; 37: 813–7PubMedCrossRef Forster SJ, Talbot IC, Clayton DG, et al. Tumour basement membrane laminin in adenocarcinoma of rectum: an immuno-histochemical study of biological andclinical significance. Int J Cancer 1986; 37: 813–7PubMedCrossRef
176.
Zurück zum Zitat Charpin C, Lissitzky JC, Jacquemier J, et al. Immunohisto-chemical detection of laminin in 98 human breast carcinomas: a light and electron microscopic study. Hum Pathol 1986; 17: 355–65PubMedCrossRef Charpin C, Lissitzky JC, Jacquemier J, et al. Immunohisto-chemical detection of laminin in 98 human breast carcinomas: a light and electron microscopic study. Hum Pathol 1986; 17: 355–65PubMedCrossRef
177.
Zurück zum Zitat Lee CS, Montebello J, Georgiou T, et al. Distribution of type IV collagen in pancreatic adenocarcinoma and chronic pancreatitis. Int J Exp Pathol 1994; 75: 79–83PubMed Lee CS, Montebello J, Georgiou T, et al. Distribution of type IV collagen in pancreatic adenocarcinoma and chronic pancreatitis. Int J Exp Pathol 1994; 75: 79–83PubMed
178.
Zurück zum Zitat Wang Z-h, Manabe T, Ohshio C, et al. Immunohistochemical study of heparan sulfate proteoglycan in adenocarcinomas of the pancreas. Pancreas 1994; 9: 758–63PubMedCrossRef Wang Z-h, Manabe T, Ohshio C, et al. Immunohistochemical study of heparan sulfate proteoglycan in adenocarcinomas of the pancreas. Pancreas 1994; 9: 758–63PubMedCrossRef
179.
Zurück zum Zitat Cottam DW, Rees RC. Regulation of matrix metalloproteinases: their role in tumor invasion and metastasis (review). Int J Oncol 1993; 2: 861–72PubMed Cottam DW, Rees RC. Regulation of matrix metalloproteinases: their role in tumor invasion and metastasis (review). Int J Oncol 1993; 2: 861–72PubMed
180.
Zurück zum Zitat Docherty AJ, Murphy C. The tissue metalloproteinase family and the inhibitor TIMP: a study using cDNAs and recombinant proteins. Ann Rheum Dis 1990; 49: 469–79PubMed Docherty AJ, Murphy C. The tissue metalloproteinase family and the inhibitor TIMP: a study using cDNAs and recombinant proteins. Ann Rheum Dis 1990; 49: 469–79PubMed
181.
Zurück zum Zitat Brown T, Tangen C, Fleming T, et al. A phase II trial of taxol and granulocyte colony stimulating factor (G-CSF) in patients with adenocarcinoma of the pancreas. Proc Am Soc Clin Oncol 1993; 12: 200 Brown T, Tangen C, Fleming T, et al. A phase II trial of taxol and granulocyte colony stimulating factor (G-CSF) in patients with adenocarcinoma of the pancreas. Proc Am Soc Clin Oncol 1993; 12: 200
182.
Zurück zum Zitat Kaue SB. Docetaxel (taxotere) in the treatment of solid tumors other than breast and lung cancer. Semin Oncol 1995; 22(4): 30–3 Kaue SB. Docetaxel (taxotere) in the treatment of solid tumors other than breast and lung cancer. Semin Oncol 1995; 22(4): 30–3
183.
Zurück zum Zitat Rougier D, DeForin M, Ademis A, et al. Phase II study of taxotere in pancreatic adenocarcinoma. Proc Am Soc Clin Oncol 1994; 13: 200 Rougier D, DeForin M, Ademis A, et al. Phase II study of taxotere in pancreatic adenocarcinoma. Proc Am Soc Clin Oncol 1994; 13: 200
184.
Zurück zum Zitat Stehlin JS, Giovanella BC, Natelson EA, et al. A study of 9-nitrocamptothecin (RFS-2000) in patients with advanced pancreatic cancer. Int J Oncol 1999; 14: 821–31PubMed Stehlin JS, Giovanella BC, Natelson EA, et al. A study of 9-nitrocamptothecin (RFS-2000) in patients with advanced pancreatic cancer. Int J Oncol 1999; 14: 821–31PubMed
186.
Zurück zum Zitat Harris AL. Anti-angiogenesis therapy and strategies for integrating it with adjuvant therapy. Recent Results Cancer Res 1998; 152: 341–52PubMedCrossRef Harris AL. Anti-angiogenesis therapy and strategies for integrating it with adjuvant therapy. Recent Results Cancer Res 1998; 152: 341–52PubMedCrossRef
Metadaten
Titel
Pancreatic Cancer
A Review of Emerging Therapies
verfasst von
Dr Lawrence Rosenberg
Publikationsdatum
01.05.2000
Verlag
Springer International Publishing
Erschienen in
Drugs / Ausgabe 5/2000
Print ISSN: 0012-6667
Elektronische ISSN: 1179-1950
DOI
https://doi.org/10.2165/00003495-200059050-00004

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