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首页> 外文期刊>OncoTargets and therapy >Survival benefit and safety of the combinations of FOLFOXIRI ± bevacizumab versus the combinations of FOLFIRI ± bevacizumab as first-line treatment for unresectable metastatic colorectal cancer: a meta-analysis
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Survival benefit and safety of the combinations of FOLFOXIRI ± bevacizumab versus the combinations of FOLFIRI ± bevacizumab as first-line treatment for unresectable metastatic colorectal cancer: a meta-analysis

机译:FOLFOXIRI±贝伐单抗组合与FOLFIRI±贝伐单抗组合作为不可切除的转移性结直肠癌一线治疗的生存获益和安全性:一项荟萃分析

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Background: The survival of patients with metastatic colorectal cancer (mCRC) could be improved with exposure to three active drugs, irinotecan, fluorouracil/leucovorin, and oxaliplatin, irrespective of their sequence. However, only 50%–80% of patients can be exposed to all the three drugs in a sequential strategy with two-drug combinations. We carried out this systematic assessment to compare the survival benefit and safety of FOLFOXIRI (irinotecan, fluorouracil/leucovorin, and oxaliplatin) ± bevacizumab (with or without bevacizumab) versus FOLFIRI (irinotecan and fluorouracil/leucovorin) ± bevacizumab (with or without bevacizumab) as first-line treatment for unresectable mCRC. Methods: PubMed and EMBASE were searched for original articles written in English and published before December 2015. A total of 1,035 patients from three randomized controlled trials were included. Results: Our results demonstrated that overall survival (hazard ratio [HR], 0.84; 95% confidence interval [CI], 0.73–0.97), progression-free survival (HR, 0.69; 95% CI, 0.59–0.81), and overall response rate (odds ratio, 1.96; 95% CI, 1.28–2.98) were significantly improved in the FOLFOXIRI ± bevacizumab arm compared to the FOLFIRI ± bevacizumab arm. Significantly higher incidences of neutropenia, anemia, diarrhea, stomatitis, and neuropathy were observed in the FOLFOXIRI ± bevacizumab arm. Conclusion: Current evidence shows that the combination of FOLFOXIRI ± bevacizumab significantly improves the overall survival, progression-free survival, and overall response rate of patients with mCRC, with an increased but manageable toxicity, compared with the combinations of FOLFIRI ± bevacizumab. The combination of FOLFOXIRI ± bevacizumab should be considered as a treatment option for these patients under the premise of reasonable selection of target population.
机译:背景:转移性结直肠癌(mCRC)患者可通过暴露于三种活性药物(伊立替康,氟尿嘧啶/亚叶酸和奥沙利铂)来提高生存率,而不论其顺序如何。但是,只有50%–80%的患者可以在采用两种药物组合的顺序策略中接触所有三种药物。我们进行了这项系统的评估,以比较FOLFOXIRI(伊立替康,氟尿嘧啶/亚叶酸和奥沙利铂)±贝伐单抗(有或没有贝伐单抗)与FOLFIRI(伊立替康和氟尿嘧啶/亚叶酸钙)±贝伐单抗(有或无贝伐单抗)的生存获益和安全性作为不可切除mCRC的一线治疗。方法:在PubMed和EMBASE中搜索英文原文并于2015年12月之前发表的文章。纳入来自三个随机对照试验的1,035例患者。结果:我们的结果表明,总体生存率(危险比[HR]为0.84; 95%置信区间[CI]为0.73-0.97),无进展生存期[HR为0.69; 95%CI为0.59–0.81]和总体与FOLFIRI±贝伐单抗组相比,FOLFOXIRI±贝伐单抗组的缓解率(比值,1.96; 95%CI,1.28–2.98)显着提高。在FOLFOXIRI±贝伐单抗组中观察到中性粒细胞减少,贫血,腹泻,口腔炎和神经病的发生率明显更高。结论:当前证据表明,与FOLFIRI±贝伐单抗联合使用FOLFOXIRI±贝伐单抗联合治疗可显着改善mCRC患者的总生存期,无进展生存期和总缓解率,且毒性增加但可控。在合理选择目标人群的前提下,应考虑将FOLFOXIRI±贝伐单抗联合使用作为这些患者的治疗选择。

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