Chen Ke, Gong Yinya, Zhang Qi, Shen Yanping, Zhou Taoqi
Department of Radiochemotherapy, Yinzhou Hospital Affiliated to Medical School of Ningbo University, Ningbo, China.
Medicine (Baltimore). 2016 Nov;95(46):e5221. doi: 10.1097/MD.0000000000005221.
Recent studies have paid much attention on the safety of bevacizumab as adjuvant chemotherapy for metastatic colorectal cancer. The aim of this meta-analysis was to study the efficacy and safety of bevacizumab in combination with irinotecan, bolus followed by infusional 5-fluorouracil, and leucovorin (FOLFIRI) and, irinotecan, bolus fluorouracil, leucovorin (IFL) for patients with metastatic colorectal cancer (mCRC).An electronic search of related trials was conducted from PubMed, EMBASE, Cochrane Library databases. Risk ratio (RRs) and its 95% confidence intervals (95% CIs) were calculated by using either DerSimonian-Laird method or Mantel-Haenszel method according to the heterogeneity of included articles. The risk of mortality, therapeutic efficacy, and adverse effect were meta-analyzed.In total, 6 RCTs including 2165 participants (1109 in the treatment group, 1056 in the control group) were included in this meta-analysis. Compared with FOLFIRI-panitumumab/cetuximab, the bevacizumab addition significantly reduced the complete response (CR) rate (RR [95%CI] = 0.31[0.11, 0.89], P = 0.03) and the risk of grade 3/4 adverse event (RR [95%CI] = 0.89[0.80, 0.98], P = 0.01). Compared with FOLFIRI and IFL alone, the addition of bevacizumb significantly increased the partial response (PR) and objective response (OR) rates. Compared with IFL alone, the addition of bevacizumb significantly reduced the mortality risk of PFS (RR [95%CI] = 0.53[0.42, 0.66], P < 0.00001) and OS (RR[95%CI] = 0.70[0.60, 0.82], P < 0.00001), but increased the risk of adverse events (RR[95%CI] = 1.14[1.06, 1.21], P = 0.0002).Combination chemotherapy of bevacizumab plus FOLFIRI or IFL had a relative high efficacy and acceptable safety for treatment of mCRC.
近期研究十分关注贝伐单抗作为转移性结直肠癌辅助化疗的安全性。本荟萃分析的目的是研究贝伐单抗联合伊立替康、推注后持续输注5-氟尿嘧啶和亚叶酸钙(FOLFIRI)以及伊立替康、推注氟尿嘧啶、亚叶酸钙(IFL)用于转移性结直肠癌(mCRC)患者的疗效和安全性。通过PubMed、EMBASE、Cochrane图书馆数据库对相关试验进行电子检索。根据纳入文章的异质性,使用DerSimonian-Laird法或Mantel-Haenszel法计算风险比(RRs)及其95%置信区间(95% CIs)。对死亡率、治疗效果和不良反应风险进行荟萃分析。本荟萃分析共纳入6项随机对照试验,包括2165名参与者(治疗组1109名,对照组1056名)。与FOLFIRI-帕尼单抗/西妥昔单抗相比,加用贝伐单抗显著降低了完全缓解(CR)率(RR [95%CI]=0.31[0.11, 0.89],P=0.03)和3/4级不良事件风险(RR [95%CI]=0.89[0.80, 0.98],P=0.01)。与单独使用FOLFIRI和IFL相比,加用贝伐单抗显著提高了部分缓解(PR)和客观缓解(OR)率。与单独使用IFL相比,加用贝伐单抗显著降低了无进展生存期(PFS)的死亡风险(RR [95%CI]=0.53[0.42, 0.66],P<0.00001)和总生存期(OS)的死亡风险(RR[95%CI]=0.70[0.60, 0.82],P<0.00001),但增加了不良事件风险(RR[95%CI]=1.14[1.06, 1.21],P=0.0002)。贝伐单抗联合FOLFIRI或IFL的联合化疗对mCRC治疗具有相对较高的疗效和可接受的安全性。