Martinez Justina, Martin Claudio, Chacon Matias, Korbenfeld Ernesto, Bella Santiago, Senna Susana, Richardet Eduardo, Coppola Federico, Bas Carlos, Hidalgo Jorge, Escobar Emiliano, Reale Monica, Smilovich Andres M, Wasserman Ernesto
Hospital Britanico, Buenos Aires, Argentina.
Am J Clin Oncol. 2006 Feb;29(1):45-51. doi: 10.1097/01.coc.0000196200.49373.d5.
Irinotecan or oxaliplatin combined with 5-fluorouracil (5-FU) +/- folinic acid (FA) has changed the treatment standards for metastatic colorectal cancer (CRC). The oxaliplatin and irinotecan combination has reported consistent activity. The purpose of this phase II study was to assess the efficacy and safety of the simultaneous administration of a triple chemotherapy combination of oxaliplatin, irinotecan, 5-FU bolus, and FA.
Eligible patients had metastatic CRC with no prior oxaliplatin or irinotecan-based chemotherapy. Treatment consisted of oxaliplatin 85 mg/m2 followed by irinotecan 150 mg/m2, repeated every 15 days, with 5-FU 500 mg/m2 bolus and FA 20 mg/m2 on days 1, 8, and 15. An early amendment suppressed the day 8 5-FU/FA.
Twenty-six eligible treated patients receiving 253 doses were assessed for toxicity. Myelosuppression was the most frequent toxicity; grade 3 to 4 neutropenia and febrile neutropenia occurred in 50% and 15% of patients, respectively. The treatment schedule modification, omitting the 5-FU dosing on day 8, considerably improved treatment compliance, reducing the incidence of febrile neutropenia, diarrhea, and asthenia. Among the 25 patients evaluable for efficacy, 10 had objective responses including 1 complete response (CR) (4%) and 9 partial responses (PR) (36%), giving an overall response rate of 40%. Median time to progression was 6.20 months [95% confidence interval (CI), 5.44-6.96]. Median overall survival was 12.95 months.
The administration of a triple combination produced promising objective responses with acceptable toxicity but does not seem to produce an evident benefit in time-related parameters.
伊立替康或奥沙利铂联合5-氟尿嘧啶(5-FU)±亚叶酸(FA)已改变了转移性结直肠癌(CRC)的治疗标准。奥沙利铂和伊立替康联合用药已显示出持续的活性。本II期研究的目的是评估奥沙利铂、伊立替康、5-FU推注和FA三联化疗联合给药的疗效和安全性。
符合条件的患者为未接受过基于奥沙利铂或伊立替康化疗的转移性CRC患者。治疗方案为奥沙利铂85mg/m²,随后伊立替康150mg/m²,每15天重复一次,在第1、8和15天给予5-FU 500mg/m²推注和FA 20mg/m²。一项早期修订取消了第8天的5-FU/FA给药。
对26例接受253剂治疗的符合条件患者进行了毒性评估。骨髓抑制是最常见的毒性反应;3至4级中性粒细胞减少和发热性中性粒细胞减少分别发生在50%和15%的患者中。治疗方案的修改,即省略第8天的5-FU给药,显著提高了治疗依从性,降低了发热性中性粒细胞减少、腹泻和乏力的发生率。在25例可评估疗效的患者中,10例有客观反应,包括1例完全缓解(CR)(4%)和9例部分缓解(PR)(36%),总缓解率为40%。中位疾病进展时间为6.20个月[95%置信区间(CI),5.44 - 6.96]。中位总生存期为12.95个月。
三联组合给药产生了有前景的客观反应,毒性可接受,但在与时间相关的参数方面似乎未产生明显益处。