Department of Clinical Pharmacy, Shenyang Pharmaceutical University, No. 103 Wenhua Road, Shenyang, 110016, Liaoning, China.
Department of Pharmacy, General Hospital of Northern Theater Command, Shenyang, China.
Drug Saf. 2021 Jan;44(1):29-40. doi: 10.1007/s40264-020-00997-2. Epub 2020 Nov 12.
Guidelines recommend combined doublet backbone chemotherapy based on 5-fluorouracil and oxaliplatin (OX) or irinotecan (IR) as the first-line treatment options for metastatic colorectal cancer. However, it is still unknown which is better when combined with bevacizumab (BEV). This systematic review and meta-analysis were performed to compare BEV-IR with BEV-OX regimens in terms of efficacy and safety.
We searched studies from databases including MEDLINE, EMBASE, CENTRAL, and conference papers. The outcomes were overall response rate, overall survival, progression-free survival, and the incidence of the most common adverse events. The dichotomous data were reported as the risk ratio (RR) and the survival outcomes were extracted as the hazard ratio with 95% confidence interval (CI).
Eleven studies including 5632 patients were identified. No difference was found in overall survival or overall response rate between BEV-IR and BEV-OX regimens. The pooled progression-free survival was significantly longer in the BEV-IR group than the BEV-OX group (hazard ratio = 0.92, 95% CI 0.87-0.98, p = 0.08). Compared with the BEV-OX group, the BEV-IR group was related to a higher risk of bleeding events (RR = 0.80, 95% CI 0.64-0.98, p = 0.03), venous thromboembolism (RR = 0.60, 95% CI 0.46-0.79, p = 0.0002), and diarrhea (RR = 0.71, 95% CI 0.62-0.80, p < 0.00001). Conversely, the BEV-OX group was related to a higher risk of thrombocytopenia (RR 2.39, 95% CI 1.67-3.42, p < 0.00001) and neuropathy (RR 3.80, 95% CI 1.90-7.64, p = 0.0002).
The BEV-IR regimen was superior in improving progression-free survival as the first-line treatment for metastatic colorectal cancer. The two different doublet regimens combined with BEV had their specific features of adverse events.
指南建议将基于氟尿嘧啶和奥沙利铂(OX)或伊立替康(IR)的联合双药骨干化疗作为转移性结直肠癌的一线治疗选择。然而,当与贝伐珠单抗(BEV)联合使用时,哪种方案更好仍不清楚。本系统评价和荟萃分析旨在比较 BEV-IR 与 BEV-OX 方案在疗效和安全性方面的差异。
我们从 MEDLINE、EMBASE、CENTRAL 和会议论文等数据库中搜索研究。结局为总缓解率、总生存期、无进展生存期和最常见不良事件的发生率。二分类数据以风险比(RR)表示,生存结局以 95%置信区间(CI)的风险比表示。
共纳入 11 项研究,包括 5632 例患者。BEV-IR 与 BEV-OX 方案在总生存期或总缓解率方面无差异。BEV-IR 组的无进展生存期明显长于 BEV-OX 组(风险比=0.92,95%CI 0.87-0.98,p=0.08)。与 BEV-OX 组相比,BEV-IR 组出血事件(RR=0.80,95%CI 0.64-0.98,p=0.03)、静脉血栓栓塞(RR=0.60,95%CI 0.46-0.79,p=0.0002)和腹泻(RR=0.71,95%CI 0.62-0.80,p<0.00001)的风险更高。相反,BEV-OX 组血小板减少症(RR 2.39,95%CI 1.67-3.42,p<0.00001)和周围神经病变(RR 3.80,95%CI 1.90-7.64,p=0.0002)的风险更高。
BEV-IR 方案作为转移性结直肠癌的一线治疗方案,在改善无进展生存期方面更具优势。两种不同的双联方案联合 BEV 具有其特定的不良反应特征。