医学
危险系数
结直肠癌
内科学
荟萃分析
置信区间
肿瘤科
胃肠病学
癌症
作者
Fausto Petrelli,Marcella Arru,Sílvia Colombo,Maria Cavallone,Fulvia Milena Cribiu’,Viola Villardita,Paola Floris,Luciano Digiesi,Gabriele Severgnini,Mariana Teixeira Moraes,Bárbara Conti,Andrea Celotti,M Viti,Andrea Sozzi
出处
期刊:Ejso
[Elsevier]
日期:2024-03-29
卷期号:50 (6): 108306-108306
被引量:1
标识
DOI:10.1016/j.ejso.2024.108306
摘要
Introduction Mutations in the BRAF gene (BRAFmut) are associated with an unfavorable prognosis in patients with metastatic colorectal cancer (CRC). The aim of this meta-analysis was to evaluate the prognosis of colorectal cancer (CRC) patients with liver metastases and the potential benefits of liver resection in patients with BRAFmut CRC. Material and methods A systematic search of PubMed, Cochrane Central Controlled Trials, and Embase databases was conducted on May 31, 2023. The inclusion criteria were as follows:1) reporting of outcomes in patients with BRAFmut CRC who underwent surgery for liver metastases and/or comparison of outcomes between those who underwent and those who did not undergo resection; 2) reporting of survival information as hazard ratios (HR); and 3) publication in English. Results 34 studies were included. Median follow up was 48 months for prognostic BRAF status meta-analysis. BRAFmut status showed a significantly increased risk of mortality (hazard ratio [HR] = 2.56, 95% confidence interval [CI] 2.04–3.22; P < 0.01) and relapse (HR = 1.97, 95% CI 1.44–2.71; P < 0.01). Resection of liver metastases was associated with a survival benefit (median follow up 46 months). The HR for survival was 0.44 (95% confidence interval [CI] 0.33–0.59; P < 0.01) in favor of surgery. Conclusions and Relevance: Our analysis indeed confirms that BRAF mutation is associated with poor survival outcomes after liver resection of CRC metastases. However, upon quantitatively assessing the survival benefit of surgical intervention in patients with BRAF-mutated CRC liver metastases, we identified a significant 56% reduction in the risk of death.
科研通智能强力驱动
Strongly Powered by AbleSci AI