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dc.creatorAgorastos, T.en
dc.creatorChatzistamatiou, K.en
dc.creatorKatsamagkas, T.en
dc.creatorKoliopoulos, G.en
dc.creatorDaponte, A.en
dc.creatorConstantinidis, T.en
dc.creatorConstantinidis, T. C.en
dc.date.accessioned2015-11-23T10:21:47Z
dc.date.available2015-11-23T10:21:47Z
dc.date.issued2015
dc.identifier10.1371/journal.pone.0119755
dc.identifier.issn19326203
dc.identifier.urihttp://hdl.handle.net/11615/25383
dc.description.abstractObjectives The objective of the present study is to assess the performance of a high-risk human papillomavirus (HR-HPV) DNA test with individual HPV-16/HPV-18 genotyping as a method for primary cervical cancer screening compared with liquid-based cytology (LBC) in a population of Greek women taking part in routine cervical cancer screening. Methods The study, conducted by the "HEllenic Real life Multicentric cErvical Screening" (HERMES) study group, involved the recruitment of 4,009 women, aged 25-55, who took part in routine cervical screening at nine Gynecology Departments in Greece. At first visit cervical specimens were collected for LBC and HPV testing using the Roche Cobas 4800 system. Women found positive for either cytology or HPV were referred for colposcopy, whereas women negative for both tests will be retested after three years. The study is ongoing and the results of the first screening round are reported herein. Results Valid results for cytology and HPV testing were obtained for 3,993 women. The overall prevalence of HR-HPV was 12.7%, of HPV-16 2.7% and of HPV-18 1.4%. Of those referred for colposcopy, cervical intraepithelial neoplasia grade 2 or worse (CIN2+) was detected in 41 women (1.07%). At the threshold of CIN2+, cytology [atypical squamous cells of undetermined significance (ASC-US) or worse] and HPV testing showed a sensitivity of 53.7%and 100% respectively, without change between age groups. Cytology and HPV testing showed specificity of 96.8% and 90.3%respectively, which was increased in older women (-30) in comparison to younger ones (25-29). Genotyping for HPV16/18 had similar accuracy to cytology for the detection of CIN2+ (sensitivity: 58.5%; specificity 97.5%) as well as for triage to colposcopy (sensitivity: 58.5% vs 53.7%for cytology). Conclusion HPV testing has much better sensitivity than cytology to identify high-grade cervical lesions with slightly lower specificity. HPV testing with individual HPV-16/HPV-18 genotyping could represent a more accurate methodology for primary cervical cancer screening in comparison to liquid-based cytology, especially in older women. © 2015 Agorastos et al.en
dc.sourcePLoS ONEen
dc.source.urihttp://www.scopus.com/inward/record.url?eid=2-s2.0-84925597699&partnerID=40&md5=08973f0b3ddb5159a8e4b42468658430
dc.subjectadulten
dc.subjectage distributionen
dc.subjectArticleen
dc.subjectbiopsy brushen
dc.subjectcancer risken
dc.subjectcancer screeningen
dc.subjectcolposcopyen
dc.subjectcontrolled clinical trialen
dc.subjectcontrolled studyen
dc.subjectdiagnostic accuracyen
dc.subjectdiagnostic test accuracy studyen
dc.subjectemergency health serviceen
dc.subjectfemaleen
dc.subjectgenotyping techniqueen
dc.subjectGreeceen
dc.subjectGreek (people)en
dc.subjecthistopathologyen
dc.subjecthumanen
dc.subjectHuman papillomavirus DNA testen
dc.subjectHuman papillomavirus type 16en
dc.subjectHuman papillomavirus type 18en
dc.subjecthuman tissueen
dc.subjectintermethod comparisonen
dc.subjectmajor clinical studyen
dc.subjectmulticenter studyen
dc.subjectpapillomavirus infectionen
dc.subjectpredictive valueen
dc.subjectprevalenceen
dc.subjectrisk assessmenten
dc.subjectsensitivity and specificityen
dc.subjectuterine cervix canceren
dc.subjectuterine cervix carcinoma in situen
dc.subjectuterine cervix cytologyen
dc.subjectvirus detectionen
dc.subjectHuman papillomavirusen
dc.titlePrimary screening for cervical cancer based on high-risk human papillomavirus (HPV) detection and HPV 16 and HPV 18 genotyping, in comparison to cytologyen
dc.typejournalArticleen


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