医学
外科肿瘤学
放射科
结直肠癌
肿瘤分期
梅德林
总体生存率
登台系统
临床试验
协议(科学)
阶段(地层学)
术前护理
内科学
肿瘤科
试验预测值
回顾性队列研究
临床意义
生存分析
结直肠外科
计算机断层摄影术
普通外科
随机对照试验
存活率
荟萃分析
直肠
文本挖掘
作者
Harpreet Kaur Sekhon Inderjit Singh,Amy Lord,Nikhil Pawa,Gina Brown
标识
DOI:10.1245/s10434-025-18371-w
摘要
BACKGROUND: Tumor deposits (TDs) identified at pathology post rectal cancer resection are increasingly recognized as an adverse prognostic factor. Advances in magnetic resonance imaging (MRI) allow for the preoperative detection of TDs (mrTDs), raising the possibility that patients with mrTDs may benefit from neoadjuvant treatment strategies or enhanced surveillance. OBJECTIVE: This meta-analysis primarily aims to evaluate the prognostic significance of mrTDs in rectal cancer patients. We also evaluate the impact of other prognostic features. METHODS: A comprehensive search was conducted in MEDLINE, Embase, and Scopus databases. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines were followed. Prognostic endpoints included disease-free survival (DFS) and overall survival (OS). Pooled hazard ratios (HR) were calculated using R software. RESULTS: Overall, 5813 and 5630 patients were included in the systematic review (13 studies) and meta-analysis (11 studies), respectively. The pooled HR for OS and DFS for mrTDs was 2.1 (95% confidence interval [CI] 1.63-2.70; p < 0.0001) and 2.13 (95% CI 1.68-2.71; p < 0.0001), respectively. The pooled HR for OS and DFS for extramural venous invasion (mrEMVI) and circumferential resection margin (mrCRM) involvement was also significantly increased (p < 0.01). The pooled HR for MRI-predicted nodal disease (mrLNMs) and T stage (mrT) for OS and DFS was insignificant (p > 0.05). CONCLUSION: This meta-analysis confirms the prognostic significance of mrTDs on OS and DFS in rectal cancer. This was also observed for mrEMVI and mrCRM, but not for mrLNMs or mrT. Current staging using TNM has poor prognostic power. A novel evidence-based staging system is needed to identify high risk patients and guide preoperative treatment strategies. Trial registration The protocol for this study was registered in the PROSPERO database (CRD420251011285).
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