Rougier P, Lepille D, Bennouna J, Marre A, Ducreux M, Mignot L, Hua A, Méry-Mignard D
Hôpital Ambroise Paré, Boulogne, France.
Ann Oncol. 2002 Oct;13(10):1558-67. doi: 10.1093/annonc/mdf259.
We have investigated the efficacy, safety and quality of life profiles of three therapeutic combinations [irinotecan + leucovorin (LV)/5-fluorouracil (5-FU), oxaliplatin + LV/5-FU and irinotecan +oxaliplatin] in patients with metastatic colorectal cancer after failure of a 5-FU-based regimen, or whose disease had progressed within 6 months of the end of treatment.
One hundred and one patients were randomised to receive either: (i) irinotecan 180 mg/m(2) on day 1 followed by an LV 200 mg/m(2) infusion, before a 5-FU 400 mg/m(2) bolus followed by a 5-FU 600 mg/m(2) infusion (LV5FU2 regimen), on days 1 and 2 every 2 weeks; (ii) oxaliplatin 85 mg/m(2) on day 1 followed by the LV5FU2 regimen on days 1 and 2 every 2 weeks; or (iii) oxaliplatin 85 mg/m(2) followed by irinotecan 200 mg/m(2), both on day 1 every 3 weeks. The primary end point was overall response rate (ORR).
The intention-to-treat ORRs were 11.4% [95% confidence interval (CI) 3.2-26.7), 21.2% (95% CI 9.0-38.9) and 15.2% (95% CI 5.1-31.9), respectively, in the three arms. Tumour growth control was >or=60% for all three combinations and overall survivals were 12.2 months (95% CI 9.2-16.0), 11.5 months (95% CI 9.0-14.1) and 11.0 months (95% CI 8.1-12.2), respectively. All patients were evaluable for safety. Main grade 3-4 toxicity was neutropenia (33 to 39% of patients).
Thus, second-line treatment with irinotecan/LV5FU2, oxaliplatin/LV5FU2 or irinotecan/oxaliplatin, provides good tumour growth control and survival coupled with an acceptable safety profile.
我们研究了三种治疗方案[伊立替康+亚叶酸钙(LV)/5-氟尿嘧啶(5-FU)、奥沙利铂+LV/5-FU和伊立替康+奥沙利铂]在接受基于5-FU方案治疗失败或治疗结束后6个月内疾病进展的转移性结直肠癌患者中的疗效、安全性和生活质量情况。
101例患者被随机分为三组接受以下治疗:(i)第1天给予伊立替康180mg/m²,随后输注亚叶酸钙200mg/m²,然后推注5-FU 400mg/m²,接着输注5-FU 600mg/m²(LV5FU2方案),每2周的第1天和第2天重复;(ii)第1天给予奥沙利铂85mg/m²,随后每2周的第1天和第2天给予LV5FU2方案;或(iii)第1天给予奥沙利铂85mg/m²,随后给予伊立替康200mg/m²,每3周的第1天重复。主要终点是总缓解率(ORR)。
三组的意向性治疗ORR分别为11.4%[95%置信区间(CI)3.2 - 26.7]、21.2%(95%CI 9.0 - 38.9)和15.2%(95%CI 5.1 - 31.9)。所有三种联合方案的肿瘤生长控制率均≥60%,总生存期分别为12.2个月(95%CI 9.2 - 16.0)、11.5个月(95%CI 9.0 - 14.1)和11.0个月(95%CI 8.1 - 12.2)。所有患者均可进行安全性评估。主要的3 - 4级毒性是中性粒细胞减少(33%至