Effectiveness of single-target fecal DNA methylation test in regional mass screening for colorectal cancer and precancerous lesions in China.

IF 4.2 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Gastroenterology Report Pub Date : 2025-04-15 eCollection Date: 2025-01-01 DOI:10.1093/gastro/goaf029
Xianhe Kong, Qiuning Wu, Zhi Zhang, Zhiqiang Yu, Feng Niu, Xianshu Wang, Hongzhi Zou
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引用次数: 0

Abstract

Background: Colorectal cancer (CRC) is the third-most-common malignancy and the second-leading cause of cancer-related deaths worldwide and current screening methods such as guaiac-based fecal occult blood test (gFOBT), fecal immunochemical test (FIT), and colonoscopy have their own pros and cons. This study aimed to assess the effectiveness of a fecal DNA methylation test by using methylated SDC2 (mSDC2) as the epigenetic biomarker for detecting CRC in a screening-naïve population.

Methods: Fecal mSDC2 test and FIT were simultaneously performed on eligible 40- to 74-year-old adults of a regional township in China. Subjects with positive results were recommended for colonoscopy. Data of positivity rates, positive predicted values (PPVs), and detection rates associated with clinical characteristics were analysed.

Results: The positivity rate of mSDC2 was 7.6% for 10,578 participants with valid results from both fecal mSDC2 test and FIT. With an adherence rate of 63.8% to colonoscopy referral, 25 CRCs, 189 advanced adenomas (AAs), and 165 non-advanced adenomas (NAAs) and polyps were detected. The PPVs of mSDC2 were 4.93%, 37.28%, and 32.54% for CRC, AA, and non-advanced lesions, respectively. When the CRCs and AAs were counted as positive findings, the fecal mSDC2 test showed a higher detective rate than FIT (relative risk [RR], 1.313 [1.129-1.528], P <0.001). When NAAs and polyps were also specified as treatable lesions, the mSDC2 test was more effective in detecting these benign growths (RR, 1.872 [1.419-2.410]; P <0.001). A combination of mSDC2 and FIT detected 29 CRCs, 298 AAs, and 234 NAAs and polyps. Overall, the fecal mSDC2 test had a higher detection rate for both advanced and non-advanced colonic lesions. The false-positive rate of the fecal mSDC2 test was comparable to that of FIT (RR, 1.169 [0.974-1.403]; P =0.113).

Conclusions: The single-target stool-based mSDC2 test can effectively and accurately detect CRC and precancerous lesions in a large-scale CRC-screening program.

Trial registration number: NCT05374369.

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单靶点粪便DNA甲基化检测在中国结直肠癌和癌前病变区域筛查中的有效性
背景:结直肠癌(CRC)是全球第三大最常见的恶性肿瘤,也是癌症相关死亡的第二大原因,目前的筛查方法,如以木聚糖为基础的粪便潜血试验(ggft)、粪便免疫化学试验(FIT)和结肠镜检查,各有利弊。本研究旨在通过甲基化SDC2 (mSDC2)作为表观遗传生物标志物,评估粪便DNA甲基化试验在screening-naïve人群中检测结直肠癌的有效性。方法:对中国某区域乡镇40 ~ 74岁成人同时进行粪便mSDC2检测和FIT检测。阳性结果的受试者建议进行结肠镜检查。分析与临床特征相关的阳性率、阳性预测值(PPVs)及检出率数据。结果:10578名参与者的mSDC2阳性率为7.6%,粪便mSDC2检测和FIT结果均有效。结肠镜转诊依从率为63.8%,共检出crc 25例,晚期腺瘤(AAs) 189例,非晚期腺瘤(NAAs)和息肉165例。mSDC2在结直肠癌、AA和非晚期病变中的ppv分别为4.93%、37.28%和32.54%。当将CRCs和AAs作为阳性结果时,粪便mSDC2检测的检出率高于FIT(相对危险度[RR] 1.313 [1.129-1.528], P 0.001)。当NAAs和息肉也被指定为可治疗的病变时,mSDC2检测更有效地检测出这些良性肿瘤(RR, 1.872 [1.419-2.410];P 0.001)。mSDC2和FIT联合检测到29例crc, 298例AAs, 234例NAAs和息肉。总的来说,粪便mSDC2检测对晚期和非晚期结肠病变的检出率都更高。粪便mSDC2检测的假阳性率与FIT相当(RR, 1.169 [0.974-1.403];p = 0.113)。结论:基于单靶点粪便的mSDC2检测可有效、准确地检测结直肠癌及癌前病变。试验注册号:NCT05374369。
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
Gastroenterology Report
Gastroenterology Report Medicine-Gastroenterology
CiteScore
4.60
自引率
2.80%
发文量
63
审稿时长
8 weeks
期刊介绍: Gastroenterology Report is an international fully open access (OA) online only journal, covering all areas related to gastrointestinal sciences, including studies of the alimentary tract, liver, biliary, pancreas, enteral nutrition and related fields. The journal aims to publish high quality research articles on both basic and clinical gastroenterology, authoritative reviews that bring together new advances in the field, as well as commentaries and highlight pieces that provide expert analysis of topical issues.
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