Oncology Unit, Oncology Department, Azienda Socio Sanitaria Territoriale Ospedale di Cremona, Cremona, Italy.
Oncology Unit, Oncology Department, Azienda Socio Sanitaria Territoriale di Bergamo Ovest, Treviglio (Bergamo), Italy.
JAMA Oncol. 2017 Jul 13;3(7):e170278. doi: 10.1001/jamaoncol.2017.0278.
The combination of fluorouracil, oxaliplatin, and irinotecan plus bevacizumab (FOLFOXIRI-Bev) is an established and effective first-line chemotherapy regimen for metastatic colorectal cancer. However, resection rates of metastases and overall survival with this schedule have never been systematically evaluated in published studies including, but not limited to, the TRIBE (TRIplet plus BEvacizumab) trial.
To assess the clinical efficacy of FOLFOXIRI-Bev, including outcomes and rates of surgical conversions.
A systematic review was conducted in October 2016 in concordance with the PRISMA guidelines of PubMed, the Cochrane Central Register of Controlled Trials, SCOPUS, Web of Science, Google Scholar, CINAHL, Ovid, and EMBASE using the terms FOLFOXIRI and bevacizumab and (colorectal cancer).
Clinical trials, retrospective case series, and prospective case series that used FOLFOXIRI-Bev for the treatment of initially unresectable metastatic colorectal cancer in humans were included. Individual case reports and retrospective case series with fewer than 10 patients were excluded.
Data were extracted independently by 2 reviewers on a predesigned, standardized form. Ultimately, data were aggregated to obtain the pooled effect size of efficacy, according to the random-effects model and weighted for the number of patients included in each trial.
Median overall survival and progression-free survival, overall response rates, and rates of R0 surgical conversions and overall surgical conversions.
Eleven FOLFOXIRI-Bev studies published between 2010 and 2016 met the inclusion criteria and were pooled for analysis. The studies included 889 patients, with 877 patients clinically evaluable for overall response rates. The objective response rate to FOLFOXIRI-Bev was 69% (95% CI, 65%-72%; I2 = 25%). The rate of overall surgical conversions was 39.1% (95% CI, 26.9%-52.8%), and the rate of R0 surgical conversions was 28.1% (95% CI, 18.1%-40.8%). Median pooled overall survival was 30.2 months (95% CI, 26.5-33.7 months) in 6 trials with data available, and progression-free survival was 12.4 months (95% CI, 10.0-14.3 months) in 9 trials with data available. In meta-regression analysis, variables significantly associated with conversion surgery were disease limited to the liver and a higher median number of cycles (close to 12).
For patients with surgically unresectable metastatic colorectal cancer, FOLFOXIRI-Bev is associated with a significant overall response rate. Such an effective regimen leads to a probability of surgical conversion of distant metastases approaching 40%, with more than one-fourth of patients having an R0 resection.
氟尿嘧啶、奥沙利铂和伊立替康联合贝伐珠单抗(FOLFOXIRI-Bev)是转移性结直肠癌的既定有效一线化疗方案。然而,在包括但不限于 TRIBE(三联加 Bevacizumab)试验在内的已发表研究中,从未系统评估过该方案的转移灶切除率和总体生存率。
评估 FOLFOXIRI-Bev 的临床疗效,包括治疗结果和手术转化率。
2016 年 10 月,根据 PRISMA 指南,在 PubMed、Cochrane 对照试验中心注册库、SCOPUS、Web of Science、Google Scholar、CINAHL、Ovid 和 EMBASE 中,使用 FOLFOXIRI 和 Bevacizumab 及(结直肠癌)等术语进行了系统评价。
纳入了使用 FOLFOXIRI-Bev 治疗初诊不可切除的转移性结直肠癌的临床试验、回顾性病例系列和前瞻性病例系列。排除了个体病例报告和少于 10 例患者的回顾性病例系列。
两位评审员独立使用预设计的标准化表格提取数据。最终,根据随机效应模型汇总数据,以获得每个试验纳入患者数量的加权疗效汇总效应量。
中位总生存期和无进展生存期、总缓解率、R0 手术转化率和总手术转化率。
2010 年至 2016 年发表的 11 项 FOLFOXIRI-Bev 研究符合纳入标准,并进行了汇总分析。这些研究共纳入 889 例患者,其中 877 例患者可用于评估总缓解率。FOLFOXIRI-Bev 的客观缓解率为 69%(95%CI,65%-72%;I2=25%)。总体手术转化率为 39.1%(95%CI,26.9%-52.8%),R0 手术转化率为 28.1%(95%CI,18.1%-40.8%)。6 项有数据的试验中,中位总生存期为 30.2 个月(95%CI,26.5-33.7 个月),9 项有数据的试验中,无进展生存期为 12.4 个月(95%CI,10.0-14.3 个月)。在元回归分析中,与手术转化率显著相关的变量是疾病局限于肝脏和中位数周期数较高(接近 12 个)。
对于手术不可切除的转移性结直肠癌患者,FOLFOXIRI-Bev 与显著的总缓解率相关。这种有效的方案导致远处转移灶手术转化率接近 40%,超过四分之一的患者可实现 R0 切除。