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dc.contributor.authorHerzog, Chiara
dc.contributor.authorMarín, Fátima
dc.contributor.authorJones, Allison
dc.contributor.authorEvans, Iona
dc.contributor.authorReisel, Daniel
dc.contributor.authorRedl, Elisa
dc.contributor.authorSchreiberhuber, Lena
dc.contributor.authorPaytubi, Sonia
dc.contributor.authorPelegrina, Beatriz
dc.contributor.authorCarmona, Álvaro
dc.contributor.authorPeremiquel-Trillas, Paula
dc.contributor.authorFrias-Gomez, Jon
dc.contributor.authorPineda, Marta
dc.contributor.authorBrunet, Joan
dc.contributor.authorPonce, Jordi
dc.contributor.authorMatias-Guiu, Xavier
dc.contributor.authorde Sanjosé, Silvia
dc.contributor.authorAlemany, Laia
dc.contributor.authorOlaitan, Adeola
dc.contributor.authorWong, Michael
dc.contributor.authorJurkovic, Davor
dc.contributor.authorCrosbie, Emma J.
dc.contributor.authorRosenthal, Adam N.
dc.contributor.authorBjørge, Line
dc.contributor.authorZikan, Michal
dc.contributor.authorDostalek, Lukas
dc.contributor.authorCibula, David
dc.contributor.authorSundström, Karin
dc.contributor.authorDillner, Joakim
dc.contributor.authorCostas, Laura
dc.contributor.authorWidschwendter, Martin
dc.date.accessioned2023-01-19T13:48:03Z
dc.date.available2023-01-19T13:48:03Z
dc.date.created2022-12-02T13:38:00Z
dc.date.issued2022
dc.identifier.issn0732-183X
dc.identifier.urihttps://hdl.handle.net/11250/3044686
dc.description.abstractPURPOSE 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. METHODS 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). RESULTS 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. CONCLUSION 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.en_US
dc.language.isoengen_US
dc.publisherASCOen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleA Simple Cervicovaginal Epigenetic Test for Screening and Rapid Triage of Women With Suspected Endometrial Cancer: Validation in Several Cohort and Case/Control Setsen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2022 American Society of Clinical Oncologyen_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.doi10.1200/JCO.22.00266
dc.identifier.cristin2087787
dc.source.journalJournal of Clinical Oncologyen_US
dc.source.pagenumber3828-3838en_US
dc.identifier.citationJournal of Clinical Oncology. 2022, 40 (33), 3828-3838.en_US
dc.source.volume40en_US
dc.source.issue33en_US


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