下一代多靶点粪便 DNA 检测试剂盒可准确检测结直肠癌和晚期癌前病变。

Zubin D Gagrat, Martin Krockenberger, Abhik Bhattacharya, Bridget Z Gagrat, Christine M Leduc, Michael B Matter, Keith D Fourrier, Douglas W Mahoney, David K Edwards V, Graham P Lidgard, Paul J Limburg, Scott C Johnson, Michael J Domanico, John B Kisiel
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引用次数: 0

摘要

多靶点粪便 DNA(mt-sDNA)检测通过分析 DNA 甲基化/突变和血红蛋白标记物,以算法得出定性结果,从而筛查结直肠癌(CRC)。最近开发出了一个新的高分辨候选甲基化DNA标记物(MDM)面板。在模拟筛查人群中,使用加权为早期 CRC 的存档粪便样本和前瞻性收集的晚期癌前病变 (APL) 评估了新型 MDM 面板和血红蛋白的性能。利用多中心病例对照研究的样本进行了标记选择 (MSS) 和单独的初步独立验证研究 (VS)。样本处理包括定向 MDM 捕获、亚硫酸氢盐转换和 MDM 定量。粪便血红蛋白采用酶联免疫吸附测定法进行定量。样本被分为 75%/25% 的训练-测试集;模型结果经过 1000 次交叉验证。所有实验室操作人员均为盲人。MSS包括232个病例(120个CRC/112个APL)和490个对照。VS包括210个病例(112个CRC/98个APL)和567个对照组;APL中86.7%为腺瘤,13.3%为无柄锯齿状病变(SSL)。平均年龄为 65.5 岁(病例)和 63.2 岁(对照组)。交叉验证 VS 对 CRC 的平均灵敏度为 95.2%,对 APL 的平均灵敏度为 57.2%,特异性分别为 89.8%(无 CRC/APL)和 92.4%(无肿瘤)。亚组分析显示,CRC 敏感性为 93.4%(I 期)和 94.2%(II 期)。APL对高级别发育不良的敏感性为82.9%,对绒毛病变的敏感性为73.4%,对管状病变的敏感性为49.8%,对SSL的敏感性为30.2%。这些数据支持下一代 mt-sDNA 检测面板的高灵敏度和特异性。一项前瞻性多中心临床验证研究(NCT04144738)将进一步评估该检测方法的性能。
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Next-generation Multi-target Stool DNA Panel Accurately Detects Colorectal Cancer and Advanced Precancerous Lesions.

The multi-target stool DNA (mt-sDNA) test screens for colorectal cancer by analyzing DNA methylation/mutation and hemoglobin markers to algorithmically derive a qualitative result. A new panel of highly discriminant candidate methylated DNA markers (MDM) was recently developed. Performance of the novel MDM panel, with hemoglobin, was evaluated in a simulated screening population using archived stool samples weighted to early-stage colorectal cancer and prospectively collected advanced precancerous lesions (APL). Marker selection study (MSS) and separate preliminary independent verification studies (VS) were conducted utilizing samples from multi-center, case-control studies. Sample processing included targeted MDM capture, bisulfite conversion, and MDM quantitation. Fecal hemoglobin was quantified using ELISA. Samples were stratified into 75%/25% training-testing sets; model outcomes were cross-validated 1,000 times. All laboratory operators were blinded. The MSS included 232 cases (120 colorectal cancer/112 APLs) and 490 controls. The VS featured 210 cases (112 colorectal cancer/98 APLs) and 567 controls; APLs were 86.7% adenomas and 13.3% sessile serrated lesions (SSL). Average age was 65.5 (cases) and 63.2 (controls) years. Mean sensitivity in the VS from cross-validation was 95.2% for colorectal cancer and 57.2% for APLs, with specificities of 89.8% (no CRC/APLs) and 92.4% (no neoplasia). Subgroup analyses showed colorectal cancer sensitivities of 93.4% (stage I) and 94.2% (stage II). APL sensitivity was 82.9% for high-grade dysplasia, 73.4% for villous lesions, 49.8% for tubular lesions, and 30.2% for SSLs. These data support high sensitivity and specificity for a next-generation mt-sDNA test panel. Further evaluation of assay performance will be characterized in a prospective, multi-center clinical validation study (NCT04144738).

Prevention relevance: This study highlights performance of the next-generation mt-sDNA test, which exhibits high sensitivity and specificity for detecting colorectal cancer and APLs. This noninvasive option has potential to increase screening participation and clinical outcomes. A multi-center, clinical validation trial is underway. See related commentary by Bresalier, p. 93.

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