Department of Epidemiology, Radboud University Nijmegen Medical Center, The Netherlands.
Anticancer Drugs. 2010 Sep;21(8):749-58. doi: 10.1097/CAD.0b013e32833c57cf.
This study was performed to obtain a comprehensive overview of the benefits and risks of second-line irinotecan monotherapy for advanced colorectal cancer. The literature was systematically reviewed to identify phase II and phase III trials that investigated the effect of second-line monotherapy with irinotecan. Thirty studies were included in this review: 25 phase II studies including 32 samples and five phase III studies including six samples. A disease control rate of greater than or equal to 50% was found in 23 out of 32 phase II samples, and one out of two phase III samples that reported disease control rate. Median time to progression was 2.7-6.0 months in phase II samples and 3.0-4.3 months in phase III samples. Median overall survival ranged from 6.6 to 16.1 months in phase II samples and 9.1-10.8 months in phase III samples. The most important severe adverse event in both phase II and phase III trials was diarrhea (5-39 and 15-36%, respectively), followed by nausea (1-24 and 5-14%), vomiting (2-22 and 6-14%), and asthenia (0-31 and 4-21%). Treatment-related mortality was 0-2% in phase II samples and 0-5% in phase III samples. Quality-of-life scores in phase II studies were associated with tumor response. In phase III studies, the quality of life while on treatment with irinotecan was similar to that of 5-fluorouracil, but better than supportive care alone. The quality of life on the weekly schedule was similar to the 3-weekly schedule. This study provides a comprehensive overview of the benefits and risks of second-line irinotecan. In general, second-line treatment with irinotecan is beneficial to patients.
本研究旨在全面了解二线伊立替康单药治疗晚期结直肠癌的获益和风险。通过系统综述,确定了评估二线伊立替康单药治疗作用的 II 期和 III 期临床试验。本综述共纳入 30 项研究:25 项 II 期研究(共纳入 32 例患者)和 5 项 III 期研究(共纳入 6 例患者)。23 项 II 期研究中有 32 例患者的疾病控制率大于等于 50%,2 项 III 期研究中有 2 例患者报告疾病控制率。II 期研究中中位无进展生存期为 2.7-6.0 个月,III 期研究中为 3.0-4.3 个月。II 期研究中中位总生存期为 6.6-16.1 个月,III 期研究中为 9.1-10.8 个月。II 期和 III 期试验中最严重的不良事件均为腹泻(分别为 5-39%和 15-36%),其次为恶心(1-24%和 5-14%)、呕吐(2-22%和 6-14%)和乏力(0-31%和 4-21%)。II 期研究中与治疗相关的死亡率为 0-2%,III 期研究中为 0-5%。II 期研究中生活质量评分与肿瘤反应相关,而 III 期研究中伊立替康治疗期间的生活质量与 5-氟尿嘧啶相似,但优于单独支持治疗。每周方案的生活质量与每 3 周方案相似。本研究全面综述了二线伊立替康的获益和风险。总体而言,二线伊立替康治疗对患者有益。