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FOLFIRI 联合贝伐珠单抗或 aFLIbercept 治疗 FOLFOX-贝伐珠单抗治疗失败的结直肠癌(BEFLICO):一项 AGE0 多中心研究。

FOLFIRI plus BEvacizumab or aFLIbercept after FOLFOX-bevacizumab failure for COlorectal cancer (BEFLICO): An AGEO multicenter study.

机构信息

Gastrointestinal Oncology Department, Hôpital Européen Georges Pompidou, AP-HP, Université de Paris, Paris, France.

Medical Oncology, Bergonié Institute, Bordeaux, France.

出版信息

Int J Cancer. 2022 Dec 1;151(11):1978-1988. doi: 10.1002/ijc.34166. Epub 2022 Jul 14.

Abstract

After failure of first line FOLFOX-bevacizumab for metastatic colorectal cancer (mCRC), adding either bevacizumab or aflibercept to second-line FOLFIRI increases survival compared to FOLFIRI alone. In this French retrospective multicentre cohort, we included patients with a mCRC treated with either FOLFIRI-aflibercept or FOLFIRI-bevacizumab. The primary endpoint was overall survival (OS), and secondary endpoints were progression-free survival (PFS), disease control rate (DCR: CR + PR + SD) and safety. We included 681 patients from 36 centers, 326 and 355 in the aflibercept and bevacizumab groups, respectively. Median age was 64.2 years and 45.2% of patients were men. Most patients had RAS-mutated tumors (80.8%) and synchronous metastases (85.7%). After a median follow up of 31.2 months, median OS was 13.0 months (95% CI: 11.3-14.7) and 10.4 months (95% CI: 8.8-11.4) in the bevacizumab and aflibercept groups, respectively (P < .0001). Median PFS was 6.0 months (95% CI: 5.4-6.5) and 5.1 months (95% CI: 4.3-5.6) (P < .0001). After adjustment on age, PS, PFS of first line, primary tumor resection, metastasis location and RAS/BRAF status, bevacizumab was still associated with better OS (HR: 0.71, 95% CI: 0.59-0.86, P = .0003). FOLFIRI-bevacizumab combination was associated with longer OS and PFS, and a better tolerability, as compared to FOLFIRI-aflibercept after progression on FOLFOX-bevacizumab.

摘要

对于转移性结直肠癌(mCRC)一线 FOLFOX-贝伐珠单抗治疗失败的患者,二线 FOLFIRI 中添加贝伐珠单抗或阿柏西普与单独使用 FOLFIRI 相比,可提高患者的总生存期(OS)。在这项法国回顾性多中心队列研究中,我们纳入了接受 FOLFIRI-阿柏西普或 FOLFIRI-贝伐珠单抗治疗的 mCRC 患者。主要终点是总生存期(OS),次要终点是无进展生存期(PFS)、疾病控制率(DCR:完全缓解+部分缓解+疾病稳定)和安全性。我们纳入了来自 36 个中心的 681 名患者,阿柏西普组和贝伐珠单抗组分别为 326 名和 355 名。中位年龄为 64.2 岁,45.2%的患者为男性。大多数患者的肿瘤存在 RAS 突变(80.8%)且为同步转移(85.7%)。中位随访 31.2 个月后,贝伐珠单抗组和阿柏西普组的中位 OS 分别为 13.0 个月(95%CI:11.3-14.7)和 10.4 个月(95%CI:8.8-11.4)(P < 0.0001)。中位 PFS 分别为 6.0 个月(95%CI:5.4-6.5)和 5.1 个月(95%CI:4.3-5.6)(P < 0.0001)。在调整年龄、PS、一线 PFS、原发肿瘤切除、转移部位和 RAS/BRAF 状态后,贝伐珠单抗仍与更好的 OS 相关(HR:0.71,95%CI:0.59-0.86,P=0.0003)。与 FOLFIRI-阿柏西普相比,FOLFIRI-贝伐珠单抗治疗在 FOLFOX-贝伐珠单抗治疗进展后,可带来更长的 OS 和 PFS 以及更好的耐受性。

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