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基于林奇综合征日本结直肠监测中致错错配修复基因突变的结直肠癌和高级腺瘤特征。

Colorectal cancer and advanced adenoma characteristics according to causative mismatch repair gene variant in Japanese colorectal surveillance for Lynch syndrome.

机构信息

Department of Gastroenterology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, 3-8-31 Ariake, Koto-hu, Tokyo, 138-8550, Japan.

The Committee of Hereditary Colorectal Cancer, Japanese Society for Cancer of the Colon and Rectum, Tokyo, Japan.

出版信息

J Gastroenterol. 2024 Aug;59(8):699-708. doi: 10.1007/s00535-024-02128-5. Epub 2024 Jun 21.

Abstract

BACKGROUND

The optimal interval of colonoscopy (CS) surveillance in cases with Lynch syndrome (LS), and stratification according to the causative mismatch repair gene mutation, has received much attention. To verify a feasible and effective CS surveillance strategy, we investigated the colorectal cancer (CRC) incidence at different intervals and the characteristics of precancerous colorectal lesions of LS cases.

METHODS

This retrospective multicenter study was conducted in Japan. CRCs and advanced adenomas (AAs) in 316 LS cases with germline pathogenic variants (path_) were analyzed according to the data of 1,756 registered CS.

RESULTS

The mean time interval for advanced CRCs (ACs) detected via CS surveillance was 28.7 months (95% confidence interval: 13.8-43.5). The rate of AC detection within (2.1%) and beyond 2 years (8.7%) differed significantly (p = 0.0003). AAs accounted for 43%, 46%, and 41% of lesions < 10 mm in size in the MLH1-, MSH2-, and MSH6-groups, respectively. The lifetime incidence of metachronous CRCs requiring intestinal resection for path_MLH1, path_MSH2, and path_MSH6 cases was 34%, 23%, and 14% in these cases, respectively. The cumulative CRC incidence showed a trend towards a 10-year delay for path_MSH6 cases as compared with that for path_MLH1 and path_MSH2 cases.

CONCLUSIONS

In cases with path_MLH1, path_MSH2, and path_MSH6, maintaining an appropriate CS surveillance interval of within 2 years is advisable to detect of the colorectal lesion amenable to endoscopic treatment. path_MSH6 cases could be stratified with path_MLH1 and MSH2 cases in terms of risk of metachronous CRC and age of onset.

摘要

背景

林奇综合征(LS)患者行结肠镜检查(CS)的最佳监测间隔时间,以及根据致病错配修复基因突变进行分层,一直备受关注。为了验证一种可行且有效的 CS 监测策略,我们研究了不同监测间隔时间 LS 患者结直肠癌(CRC)的发生率和癌前结直肠病变的特征。

方法

这是一项在日本进行的回顾性多中心研究。根据 1756 例已注册 CS 的资料,对 316 例携带种系致病性变异(path_)的 LS 患者的 CRC 和高级腺瘤(AA)进行分析。

结果

通过 CS 监测发现的晚期 CRC(AC)的平均时间间隔为 28.7 个月(95%置信区间:13.8-43.5)。在 2 年内(2.1%)和超过 2 年(8.7%)检测到 AC 的比例有显著差异(p = 0.0003)。在大小<10mm 的病变中,AA 分别占 MLH1-、MSH2-和 MSH6-组的 43%、46%和 41%。path_MLH1、path_MSH2 和 path_MSH6 患者需要肠切除的 MLH1、MSH2 和 MSH6 病例的异时性 CRC 的终生发生率分别为 34%、23%和 14%。CRC 累积发生率显示,path_MSH6 病例比 path_MLH1 和 path_MSH2 病例的 CRC 发病时间延迟了 10 年。

结论

在 path_MLH1、path_MSH2 和 path_MSH6 患者中,建议将 CS 监测间隔保持在 2 年内,以便发现可进行内镜治疗的结直肠病变。path_MSH6 病例可以与 path_MLH1 和 MSH2 病例一起根据异时性 CRC 的风险和发病年龄进行分层。

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