A Simple Cervicovaginal Epigenetic Test for Screening and Rapid Triage of Women With Suspected Endometrial Cancer: Validation in Several Cohort and Case/Control Sets

医学 子宫内膜癌 队列 急诊分诊台 产科 妇科 宫颈癌 入射(几何) 队列研究 癌症 前瞻性队列研究 内科学 光学 物理 急诊医学
作者
Chiara Herzog,Fátima Marín,Allison Jones,Iona Evans,Daniel Reisel,Elisa Redl,Lena Schreiberhuber,Sònia Paytubi,Beatriz Pelegrina,Álvaro Carmona,Paula Peremiquel-Trillas,Jon Frias-Gomez,Marta Pineda,Joan Brunet,Jordi Ponce,Xavier Matías‐Guiu,Sílvia de Sanjosé,Laia Alemany,Adeola Olaitan,Michael L. Wong,D. Jurkovic,Emma J. Crosbie,Alan D. Rosenthal,Line Bjørge,Michal Zikán,Lukáš Dostálek,David Cibula,Karin Sundström,Joakim Dillner,Laura Costas,Martin Widschwendter
出处
期刊:Journal of Clinical Oncology [American Society of Clinical Oncology]
卷期号:40 (33): 3828-3838 被引量:17
标识
DOI:10.1200/jco.22.00266
摘要

Endometrial cancer (EC) incidence has been rising over the past 10 years. Delays in diagnosis reduce survival and necessitate more aggressive treatment. We aimed to develop and validate a simple, noninvasive, and reliable triage test for EC to reduce the number of invasive diagnostic procedures and improve patient survival.We developed a test to screen and triage women with suspected EC using 726 cervical smear samples from women with and without EC, and validated the test in 562 cervicovaginal samples using three different collection methods (cervical smear: n = 248; vaginal swab: n = 63; and self-collection: n = 251) and four different settings (case/control: n = 388; cohort of women presenting with postmenopausal bleeding: n = 63; a cohort of high-risk women with Lynch syndrome: n = 25; and a nested case/control setting from a screening cohort and samples taken up to 3 years before EC diagnosis: n = 86).We describe the Women's cancer risk IDentification - quantitative polymerase chain reaction test for Endometrial Cancer (WID-qEC), a three-marker test that evaluates DNA methylation in gene regions of GYPC and ZSCAN12. In cervical, self-collected, and vaginal swab samples derived from symptomatic patients, it detected EC with sensitivities of 97.2% (95% CI, 90.2 to 99.7), 90.1% (83.6 to 94.6), and 100% (63.1 to 100), respectively, and specificities of 75.8% (63.6 to 85.5), 86.7% (79.3 to 92.2), and 89.1% (77.8 to 95.9), respectively. The WID-qEC identified 90.9% (95% CI, 70.8 to 98.9) of EC cases in samples predating diagnosis up to 1 year. Test performance was similar across menopausal status, age, stage, grade, ethnicity, and histology.The WID-qEC is a noninvasive reliable test for triage of women with symptoms suggestive of ECs. Because of the potential for self-collection, it could improve early diagnosis and reduce the reliance for in-person visits.

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