Risk of metachronous neoplasia in early-onset colorectal cancer: meta-analysis.

IF 3.5 3区 医学 Q1 SURGERY
BJS Open Pub Date : 2024-09-03 DOI:10.1093/bjsopen/zrae092
Gianluca Pellino, Giacomo Fuschillo, Rogelio González-Sarmiento, Marc Martí-Gallostra, Francesco Selvaggi, Eloy Espín-Basany, Jose Perea
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Abstract

Background: Metachronous colorectal cancer refers to patients developing a second colorectal neoplasia diagnosed at least 6 months after the initial cancer diagnosis, excluding recurrence. The aim of this systematic review is to assess the incidence of metachronous colorectal cancer in early-onset colorectal cancer (defined as age at diagnosis of less than 50 years) and to identify risk factors.

Methods: This is a systematic review and meta-analysis performed following the PRISMA statement and registered on PROSPERO. The literature search was conducted in PubMed and Embase. Only studies involving patients with early-onset colorectal cancer (less than 50 years old) providing data on metachronous colorectal cancer were included in the analysis. The primary endpoint was the risk of metachronous colorectal cancer in patients with early-onset colorectal cancer. Secondary endpoints were association with Lynch syndrome, family history and microsatellite instability.

Results: Sixteen studies met the inclusion criteria. The incidence of metachronous colorectal cancer was 2.6% (95% c.i. 2.287-3.007). The risk of developing metachronous colorectal cancer in early-onset colorectal cancer versus non-early-onset colorectal cancer patients demonstrated an OR of 0.93 (95% c.i. 0.760-1.141). The incidence of metachronous colorectal cancer in patients with Lynch syndrome was 18.43% (95% c.i. 15.396-21.780), and in patients with family history 10.52% (95% c.i. 5.555-17.659). The proportion of metachronous colorectal cancer tumours in the microsatellite instability population was 19.7% (95% c.i. 13.583-27.2422).

Conclusion: The risk of metachronous colorectal cancer in patients with early-onset colorectal cancer is comparable to those with advanced age, but it is higher in patients with Lynch syndrome, family history and microsatellite instability. This meta-analysis demonstrates the need to personalize the management of patients with early-onset colorectal cancer according to their risk factors.

早发性结直肠癌的远期肿瘤风险:荟萃分析。
背景:同期性结直肠癌是指患者在初次确诊癌症至少 6 个月后再次确诊结直肠肿瘤(不包括复发)。本系统综述的目的是评估早发结直肠癌(定义为诊断时年龄小于 50 岁)中近端结直肠癌的发病率,并确定风险因素:这是一项按照 PRISMA 声明进行的系统性综述和荟萃分析,已在 PROSPERO 上注册。文献检索在 PubMed 和 Embase 上进行。只有涉及早发结直肠癌患者(年龄小于 50 岁)的研究才会被纳入分析,这些研究提供了有关变异性结直肠癌的数据。主要终点是早发结直肠癌患者罹患变异性结直肠癌的风险。次要终点是与林奇综合征、家族史和微卫星不稳定性的关系:结果:16 项研究符合纳入标准。变异性结直肠癌的发病率为 2.6%(95% 置信区间为 2.287-3.007)。早发性结直肠癌患者与非早发性结直肠癌患者相比,罹患变异性结直肠癌的风险OR值为0.93(95% 置信区间:0.760-1.141)。林奇综合征患者的远期结直肠癌发病率为 18.43%(95% 置信区间为 15.396-21.780),有家族史的患者的发病率为 10.52%(95% 置信区间为 5.555-17.659)。在微卫星不稳定人群中,远缘结直肠癌肿瘤的比例为 19.7%(95% 置信区间:13.583-27.2422):结论:早发结直肠癌患者罹患转移性结直肠癌的风险与高龄患者相当,但林奇综合征、家族史和微卫星不稳定性患者的风险更高。这项荟萃分析表明,有必要根据早发结直肠癌患者的风险因素对其进行个性化管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BJS Open
BJS Open SURGERY-
CiteScore
6.00
自引率
3.20%
发文量
144
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