Phase II study of second-line oxaliplatin, irinotecan and mitomycin C in patients with advanced or metastatic colorectal cancer

被引:9
作者
Hejna, M
Köstler, WJ
Raderer, M
Tomek, S
Brodowicz, T
Scheithauer, W
Wiltschke, C
Zielinski, CC
机构
[1] Univ Hosp Vienna, Dept Med 1, Chair Med Expt Oncol, A-1090 Vienna, Austria
[2] Univ Hosp Vienna, Dept Med 1, Div Oncol, A-1090 Vienna, Austria
[3] Ludwig Boltzmann Inst Clin Expt Oncol, A-1090 Vienna, Austria
关键词
colorectal cancer; irinotecan; mitomycin C; oxaliplatin;
D O I
10.1097/00001813-200009000-00005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this phase II study was to investigate the therapeutic value of second-line treatment with oxaliplatin, irinotecan (CPT-11) and mitomycin C (MMC) in patients with metastatic colorectal cancer pretreated with 5-fluorouracil (5-FU)-based chemotherapy. A total of 10 patients with metastatic colorectal cancer, all of whom had developed progressive disease from advanced or metastatic colorectal cancer while receiving or within 6 months after discontinuing first-line chemotherapy with 5-FU and leucovorin, were entered in this study. At the time of relapse, cytotoxic chemotherapy consisting of oxaliplatin 80 mg/m(2) plus CPT-11 80 mg/m(2) given i.v. on therapeutic day 1, and MMC 6 mg/m(2) given i.v, on day 15, respectively, was initiated. Treatment courses were repeated every 4 weeks for a total of six courses unless there was prior evidence of progressive disease. The overall response rate was 30% with three partial responses for all 10 assessable patients. Two additional patients (20%) had stable disease and five patients (50%) progressed. The median overall survival duration has not been reached yet and is longer than 7.1 months (range 2-23.5+) from the beginning of second-line therapy. Four patients are currently alive with progressive disease. The tolerance of second-line treatment was generally mild to moderate and easy to treat. Our data suggest that the combination of oxaliplatin, CPT-11 and MMC in patients with metastatic colorectal cancer pretreated with 5-FU-based chemotherapy is feasible and has substantial antitumor activity. Further evaluation of this regimen seems warranted. [ (C) 2000 Lippincott Williams & Wilkins.].
引用
收藏
页码:629 / 634
页数:6
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