Department of Oncology, The Affiliated Nanjing First Hospital, Nanjing Medical University, Nanjing, PR China.
Oncol Res. 2010;18(9):437-44. doi: 10.3727/096504010x12671222663511.
A large number of randomized controlled trials involving chemotherapy in the management of advanced colorectal cancer were conducted. 5-FU/LV in combination with irinotecan (IRI) or oxaliplatin (OXA) was used. The aim of the meta-analysis was to compare and evaluate the effectiveness and safety of the two therapeutic approaches for patients with advanced colorectal cancer. A literature search, study selection and assessment, data collection, and analysis were undertaken by two reviewers according to the Cochrane Handbook for Systematic Reviews of Interventions. Randomized controlled trials (RCTs) or quasi-RCTs comparing IRI versus OXA, in combination with 5-FU/LV in the treatment of advanced colorectal cancer were performed. Seven studies involving 2,107 patients met the inclusion criteria. The OXA + 5-FU/LV regimen showed a significant increase in survival by lower hazard ratios (HR) [HR 1.28; 95% CI (1.13-1.45)] and was associated with lower toxicities. The OXA + 5-FU/LV regimen was superior or equal to the IRI + 5-FU/LV regimen in prolonging time to progression and median survival. The IRI + 5-FU/LV regimen resulted in higher hazard ratios in nausea vomiting/emesis and diarrhea [HR 1.99, 95% CI (1.19-3.31); HR 1.83, 95% CI (1.38-2.44)] and lower hazard ratios in paresthesia, sensory neuropathy, and thrombocytopenia [HR 0.09, 95% CI (0.03-0.23); HR 0.04 95% CI (0.01-0.13); HR 0.19 95% CI (0.05-0.64)] than the OXA + 5-FU/LV regimen. Compared with IRI, OXA is more appropriate for the treatment of advanced colorectal cancer when combined with 5-FU/LV. OXA + 5-FU/LV should be considered as the first-line standard of care for advanced CRC patients.
进行了大量涉及化疗治疗晚期结直肠癌的随机对照试验。5-FU/LV 联合伊立替康(IRI)或奥沙利铂(OXA)用于治疗。该荟萃分析的目的是比较和评估这两种治疗方法对晚期结直肠癌患者的有效性和安全性。两名评审员根据 Cochrane 系统评价干预手册进行文献检索、研究选择和评估、数据收集和分析。比较 IRI 与 OXA 联合 5-FU/LV 治疗晚期结直肠癌的随机对照试验(RCTs)或准 RCTs 进行了比较。有 7 项研究共纳入 2107 例患者符合纳入标准。OXA + 5-FU/LV 方案的生存风险比(HR)较低,具有显著的生存优势[HR 1.28;95%置信区间(1.13-1.45)],且毒性较低。OXA + 5-FU/LV 方案在延长无进展生存期和中位生存期方面优于或等同于 IRI + 5-FU/LV 方案。IRI + 5-FU/LV 方案在恶心呕吐/呕吐和腹泻方面导致更高的 HR[HR 1.99,95%置信区间(1.19-3.31);HR 1.83,95%置信区间(1.38-2.44)],而在感觉异常、感觉神经病变和血小板减少方面导致更低的 HR[HR 0.09,95%置信区间(0.03-0.23);HR 0.04,95%置信区间(0.01-0.13);HR 0.19,95%置信区间(0.05-0.64)]。与 OXA + 5-FU/LV 方案相比,IRI 联合 5-FU/LV 治疗晚期结直肠癌更合适。OXA + 5-FU/LV 应被视为晚期 CRC 患者的一线治疗标准。