Schüll B, Kornek G V, Schmid K, Raderer M, Ulrich-Pur H, Fiebiger W, Schneeweiss B, Lenauer A, Depisch D, Scheithauer W
Division of Oncology, Department of Internal Medicine I, University Medical School, Vienna, Austria.
Onkologie. 2002 Aug;25(4):358-62. doi: 10.1159/000066054.
Both oxaliplatin and irinotecan have demonstrated antitumor activity in pretreated colorectal cancer; experimental and early clinical data suggest that these two drugs may act synergistically. The aim of this study was to document the therapeutic index of a biweekly combination regimen in patients with metastatic colorectal cancer failing prior palliative first-line chemotherapy with raltitrexed.
In this study 27 patients with metastatic colorectal cancer were analyzed, who progressed while on or within 6 months after discontinuation of palliative first-line chemotherapy with raltitrexed. They received oxaliplatin 85 mg/m(2) and irinotecan 150 mg/m(2) both given on days 1 and 15 every 4 weeks.
The confirmed overall response rate was 37% (95% confidence interval, 19.4-57.7%), including 2 complete and 8 partial remissions. 12 additional patients (44.4%) had stable disease, and in only 5 cases (18.5%) disease progression was not influenced by chemotherapy. The median progression-free survival for all 27 patients was 8 months (range, 1-16+ months), and 16 patients (59%) are still alive after a median follow-up time of 12.5 months. Hematologic adverse reactions, specifically leukocytopenia and neutropenia, were common though generally mild to moderate with grade 4 toxicity occurring in only 2 cases. The most frequent non-hematologic adverse events included gastrointestinal symptoms; severe nausea/emesis and diarrhea, however, were noted in only 2 and 3 patients, respectively.
Our data suggest that the described biweekly combination regimen of oxaliplatin and irinotecan has substantial antitumor activity in patients with progressive, raltitrexed-pretreated metastatic colorectal cancer. Because of its favorable toxicity profile, further evaluation of this combination seems warranted.
奥沙利铂和伊立替康在经治的结直肠癌中均已显示出抗肿瘤活性;实验及早期临床数据表明这两种药物可能具有协同作用。本研究的目的是记录在先前接受雷替曲塞姑息性一线化疗失败的转移性结直肠癌患者中,每两周一次联合方案的治疗指数。
本研究分析了27例转移性结直肠癌患者,这些患者在接受雷替曲塞姑息性一线化疗期间或停药后6个月内病情进展。他们每4周在第1天和第15天接受奥沙利铂85mg/m²和伊立替康150mg/m²治疗。
确认的总缓解率为37%(95%置信区间,19.4 - 57.7%),包括2例完全缓解和8例部分缓解。另外12例患者(44.4%)病情稳定,只有5例(18.5%)疾病进展不受化疗影响。所有27例患者的无进展生存期中位数为8个月(范围,1 - 16 +个月),在中位随访时间12.5个月后,16例患者(59%)仍存活。血液学不良反应,特别是白细胞减少和中性粒细胞减少很常见,但一般为轻至中度,4级毒性仅发生在2例患者中。最常见的非血液学不良事件包括胃肠道症状;然而,严重恶心/呕吐和腹泻分别仅在2例和3例患者中出现。
我们的数据表明,所描述的奥沙利铂和伊立替康每两周一次联合方案在雷替曲塞预处理的进展期转移性结直肠癌患者中具有显著的抗肿瘤活性。由于其良好的毒性特征,似乎有必要对该联合方案进行进一步评估。