Passiglia Francesco, Bronte Giuseppe, Bazan Viviana, Galvano Antonio, Vincenzi Bruno, Russo Antonio
Department of Surgical, Oncological and Oral Sciences, Section of Medical Oncology, University of Palermo, Palermo, Italy.
Medical Oncology Department, Campus Biomedico, University of Rome, Rome, Italy.
Crit Rev Oncol Hematol. 2016 Mar;99:150-7. doi: 10.1016/j.critrevonc.2015.12.015. Epub 2016 Jan 2.
Clinical trials investigated the potential role of both KRAS and BRAF mutations, as prognostic biomarkers, in colorectal cancer (CRC) patients who underwent surgical treatment of CRC-related liver metastases (CLM), showing conflicting results. This meta-analysis aims to review all the studies reporting survival outcomes (recurrence free survival (RFS), and/or overall survival (OS)) of patients undergoing resection of CLM, stratified according to KRAS and/or BRAF mutation status.
Data from all published studies reporting survival outcomes (RFS and/or OS) of CRC patients who received resection of CLM, stratified by KRAS and/or BRAF mutation status were collected, according to the PRISMA guidelines. Pooled HRs were calculated for both the OS and/or RFS.
Seven eligible trials (1403 patients) were included. Pooled analysis showed that KRAS mutations predicted a significantly worse both RFS (HR: 1.65; 95% CI: 1.23-2.21) and OS (HR: 1.86; 95% CI: 1.51-2.30) in patients who underwent surgical resection of CLM. BRAF mutations were also associated with a significantly worse OS (HR: 3.90; 95% CI: 1.96-7.73) in this subgroup of patients.
This meta-analysis suggests both KRAS and BRAF mutations as poor, prognostic biomarkers, associated with worse survival outcomes, in patients undergoing hepatic resection of CLM.
临床试验研究了KRAS和BRAF突变作为预后生物标志物在接受结直肠癌相关肝转移(CLM)手术治疗的结直肠癌(CRC)患者中的潜在作用,结果相互矛盾。本荟萃分析旨在回顾所有报告CLM切除患者生存结局(无复发生存期(RFS)和/或总生存期(OS))的研究,并根据KRAS和/或BRAF突变状态进行分层。
根据PRISMA指南,收集所有已发表的报告CLM切除的CRC患者生存结局(RFS和/或OS)的数据,并根据KRAS和/或BRAF突变状态进行分层。计算OS和/或RFS的合并风险比(HR)。
纳入了7项符合条件的试验(1403例患者)。汇总分析显示,在接受CLM手术切除的患者中,KRAS突变预示RFS(HR:1.65;95%CI:1.23-2.21)和OS(HR:1.86;95%CI:1.51-2.30)均显著较差。在该亚组患者中,BRAF突变也与OS显著较差相关(HR:3.90;95%CI:1.96-7.73)。
本荟萃分析表明,在接受CLM肝切除的患者中,KRAS和BRAF突变均为不良预后生物标志物,与较差的生存结局相关。