Scheithauer W, Kornek G V, Raderer M, Valencak J, Weinländer G, Hejna M, Haider K, Kwasny W, Depisch D
Department of Internal Medicine I, University Medical School, Vienna, Austria.
J Clin Oncol. 1999 Mar;17(3):902-6. doi: 10.1200/JCO.1999.17.3.902.
To evaluate the efficacy and tolerance of combined irinotecan and oxaliplatin in patients with advanced colorectal cancer pretreated with leucovorin-modulated fluoropyrimidines.
Thirty-six patients with metastatic colorectal cancer, who progressed while receiving or within 6 months after discontinuing palliative chemotherapy with fluoropyrimidines/leucovorin, were enrolled onto this study. Treatment consisted of oxaliplatin 85 mg/m2 on days 1 + 15 and irinotecan 80 mg/m2 on days 1 + 8 + 15 every 4 weeks. Depending on the absolute neutrophil counts (ANC) on the day of scheduled chemotherapeutic drug administration, a 5-day course of granulocyte colony-stimulating factor (G-CSF) 5 microg/kg/d was given.
The overall response rate was 42% for all 36 assessable patients (95% confidence interval, 26% to 59%), including two complete remissions (6%). Thirteen additional patients (36%) had stable disease, and only eight (22%) progressed. The median time to treatment failure was 7.5 months (range, 1 to 13.5+ months). After a median follow-up time of 14 months, 19 patients (53%) are still alive. Hematologic toxicity was commonly observed, although according to the ANC-adapted use of G-CSF (in 31 patients during 81 of 174 courses), it was generally mild: grade 3 and 4 granulocytopenia occurred in only five and two cases, respectively. The most frequent nonhematologic adverse reactions were nausea/emesis and diarrhea, which were rated severe in 17% and 19%, respectively.
Our data suggest that the combination of irinotecan and oxaliplatin with or without G-CSF has substantial antitumor activity in patients with progressive fluoropyrimidine/leucovorin-pretreated colorectal cancer. Overall toxicity was modest, with gastrointestinal symptoms constituting the dose-limiting side effects. Further evaluation of this regimen seems warranted.
评估伊立替康联合奥沙利铂用于接受亚叶酸钙调节的氟嘧啶预处理的晚期结直肠癌患者的疗效和耐受性。
36例转移性结直肠癌患者入组本研究,这些患者在接受氟嘧啶/亚叶酸钙姑息化疗期间或停药后6个月内病情进展。治疗方案为每4周的第1天和第15天给予奥沙利铂85mg/m²,第1天、第8天和第15天给予伊立替康80mg/m²。根据预定化疗药物给药当天的绝对中性粒细胞计数(ANC),给予5天疗程的粒细胞集落刺激因子(G-CSF),剂量为5μg/kg/d。
36例可评估患者的总体缓解率为42%(95%置信区间,26%至59%),包括2例完全缓解(6%)。另有13例患者(36%)病情稳定,仅8例(22%)病情进展。治疗失败的中位时间为7.5个月(范围,1至13.5+个月)。中位随访时间14个月后,19例患者(53%)仍存活。血液学毒性常见,不过根据ANC调整使用G-CSF(174个疗程中的81个疗程,31例患者),毒性一般较轻:3级和4级粒细胞减少分别仅发生5例和2例。最常见的非血液学不良反应是恶心/呕吐和腹泻,分别有17%和19%的患者症状严重。
我们的数据表明,伊立替康和奥沙利铂联合或不联合G-CSF对接受氟嘧啶/亚叶酸钙预处理且病情进展的结直肠癌患者具有显著的抗肿瘤活性。总体毒性适中,胃肠道症状为剂量限制性副作用。该方案似乎有必要进一步评估。