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荷兰广泛与部分结肠切除术治疗后林奇综合征致病性变异体患者的异时性结直肠癌风险:一项回顾性队列研究。

Metachronous colorectal cancer risk according to Lynch syndrome pathogenic variant after extensive versus partial colectomy in the Netherlands: a retrospective cohort study.

机构信息

Department of Gastroenterology and Hepatology, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, Netherlands; Department of Clinical Genetics, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, Netherlands.

Department of Gastroenterology and Hepatology, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, Netherlands.

出版信息

Lancet Gastroenterol Hepatol. 2023 Dec;8(12):1106-1117. doi: 10.1016/S2468-1253(23)00228-5. Epub 2023 Oct 18.

Abstract

BACKGROUND

Extensive colectomy (subtotal or total colectomy) is often advised for carriers of Lynch syndrome with colorectal cancer. However, the risk of metachronous colorectal cancer might differ by Lynch syndrome variant, meaning that partial colectomy, which has better functional outcomes, might be adequate for some patients with low-risk variants. We aimed to assess the risk of metachronous colorectal cancer after partial colectomy and extensive colectomy in carriers of Lynch syndrome with different pathogenic variants.

METHODS

For this retrospective cohort study, carriers of Lynch syndrome with colorectal cancer in the Netherlands were identified by linkage of the Dutch Foundation for the Detection of Hereditary Tumors (StOET) database and the Dutch Nationwide Network and Registry of Histopathology and Cytopathology (PALGA) database. Data on demographics, Lynch syndrome variants, colorectal cancers, surgery types, mortality, and surveillance colonoscopies were extracted. Data on colorectal cancer and surveillance colonoscopies were updated until Feb 28, 2022. Data on survival status was updated until Feb 7, 2022. MLH1, MSH2, and EPCAM were classified as high-risk variants and MSH6 and PMS2 as low-risk variants. Patients for whom the type of surgery was unknown were excluded. Cox regression time-to-event analyses were done to assess the risk of metachronous colorectal cancer in four subgroups based on pathogenic variant (high-risk vs low-risk variants) and the extent of surgery (extensive colectomy vs partial colectomy). Sex, age at the time of primary colorectal cancer, primary colorectal cancer stage, performance of surveillance colonoscopies, adherence to the surveillance guidelines, and time period of primary colorectal cancer diagnosis were added to the model as possible confounders. Metachronous colorectal cancer was defined as colorectal cancer diagnosed more than 6 months after the primary colorectal cancer. Patients were censored at time of death or assembly of the database.

FINDINGS

Of 1908 carriers of Lynch syndrome registered in StOET, 532 with a history of colorectal cancer were identified after linkage with PALGA. Five carriers were excluded because of an unknown surgery type, leaving 527 in our sample (mean age at primary colorectal cancer 48·7 years [SD 12·1]; 274 [52%] male and 253 [48%] female). 121 (23%) patients developed metachronous colorectal cancer (median time from primary colorectal cancer to metachronous colorectal cancer 11·0 years [IQR 2·1-17·8]). Metachronous colorectal cancer occurred in 12 (12%) of 97 patients with high-risk variants and extensive colectomy, in 85 (32%) of 267 patients with high-risk variants and partial colectomy, in zero (0%) of 11 patients with low-risk variants and extensive colectomy, and in 24 (16%) of 152 patients with low-risk variants and partial colectomy. Partial colectomy was associated with a higher risk of metachronous colorectal cancer than extensive colectomy in the high-risk variant group (hazard ratio 1·97, 95% CI 1·04-3·73; p=0·039). The risk of metachronous colorectal cancer did not differ between carriers of low-risk variants who had partial colectomy and those of high-risk variants who had extensive colectomy (1·14, 0·55-2·36; p=0·72).

INTERPRETATION

The risk of metachronous colorectal cancer after partial colectomy in carriers of low-risk variants is similar to the risk after extensive colectomy in carriers of high-risk variants. This finding suggests that partial colectomy followed by endoscopic surveillance is an appropriate management approach to treat colorectal cancer in carriers of low-risk Lynch syndrome variants.

FUNDING

None.

摘要

背景

对于携带林奇综合征的结直肠癌患者,通常建议进行广泛结肠切除术(次全或全结肠切除术)。然而,不同林奇综合征变异体的患者发生异时性结直肠癌的风险可能不同,这意味着对于低危变异体的一些患者,部分结肠切除术(具有更好的功能结果)可能就足够了。我们旨在评估不同致病性变异体的林奇综合征携带者进行部分结肠切除术和广泛结肠切除术之后发生异时性结直肠癌的风险。

方法

本回顾性队列研究通过荷兰肿瘤遗传检测基金会(StOET)数据库和荷兰全国组织和病理细胞学登记处(PALGA)数据库的链接,确定了荷兰携带林奇综合征的结直肠癌患者。提取了人口统计学、林奇综合征变异体、结直肠癌、手术类型、死亡率和监测结肠镜检查等数据。截至 2022 年 2 月 28 日更新了结直肠癌和监测结肠镜检查的数据,截至 2022 年 2 月 7 日更新了生存状况的数据。MLH1、MSH2 和 EPCAM 被归类为高危变异体,MSH6 和 PMS2 为低危变异体。对于未知手术类型的患者,则将其排除在外。采用 Cox 回归时间事件分析,根据致病性变异体(高危变异体与低危变异体)和手术范围(广泛结肠切除术与部分结肠切除术)将患者分为四个亚组,评估异时性结直肠癌的风险。性别、原发性结直肠癌时的年龄、原发性结直肠癌分期、进行监测结肠镜检查、遵循监测指南和原发性结直肠癌诊断时间被添加到模型中作为可能的混杂因素。异时性结直肠癌定义为原发性结直肠癌诊断后 6 个月以上诊断的结直肠癌。患者以死亡或数据库组合时间为截止点。

结果

在 StOET 注册的 1908 名携带林奇综合征的患者中,通过与 PALGA 链接,确定了 532 名有结直肠癌病史的患者。由于手术类型未知,排除了 5 名患者,在我们的样本中留下 527 名患者(原发性结直肠癌时的平均年龄 48.7 岁[SD 12.1];男性 274 名[52%],女性 253 名[48%])。121 名(23%)患者发生异时性结直肠癌(从原发性结直肠癌到异时性结直肠癌的中位数时间为 11.0 年[IQR 2.1-17.8])。12 名(12%)高危变异体和广泛结肠切除术患者、85 名(32%)高危变异体和部分结肠切除术患者、11 名(0%)低危变异体和广泛结肠切除术患者以及 152 名(16%)低危变异体和部分结肠切除术患者发生异时性结直肠癌。高危变异体组中,部分结肠切除术与广泛结肠切除术相比,发生异时性结直肠癌的风险更高(风险比 1.97,95%CI 1.04-3.73;p=0.039)。在低危变异体患者中,部分结肠切除术与高危变异体患者广泛结肠切除术相比,发生异时性结直肠癌的风险无差异(1.14,0.55-2.36;p=0.72)。

结论

低危变异体携带者行部分结肠切除术之后发生异时性结直肠癌的风险与高危变异体携带者行广泛结肠切除术之后发生异时性结直肠癌的风险相似。这一发现表明,对于低危林奇综合征变异体携带者,行部分结肠切除术联合内镜监测是一种合适的治疗方法。

资金

无。

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