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dc.rights.licenseopenen_US
dc.contributor.authorDEBEAUDRAP, Pierre
dc.contributor.authorKABORE, Firmin Nongodo
dc.contributor.authorSETHA, Limsreng
dc.contributor.authorTEGBE, Joseph
dc.contributor.authorDOUKOURE, Brahima
dc.contributor.authorSOTHEARA, Moeung
dc.contributor.authorSEGERAL, Olivier
dc.contributor.authorAUN, Korn
dc.contributor.authorMESSOU, Eugene
dc.contributor.authorBITOLOG, Pauline
dc.contributor.authorSOTHEA, Kim
dc.contributor.authorVASSILAKOS, Pierre
dc.contributor.authorPODA, Armel
dc.contributor.authorPODA, Evelyn Kasile
hal.structure.identifierBordeaux population health [BPH]
hal.structure.identifierGlobal Health in the Global South [GHiGS]
dc.contributor.authorJAQUET, Antoine
dc.contributor.authorSOME, Adolphe
dc.contributor.authorPETIGNAT, Patrick
dc.contributor.authorCLIFFORD, Gary
dc.contributor.authorHORO, Apollinaire
dc.date.accessioned2024-10-18T08:23:41Z
dc.date.available2024-10-18T08:23:41Z
dc.date.issued2024-09-25
dc.identifier.issn0020-7136en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/202574
dc.description.abstractEnThe WHO recommends the use of human papillomavirus (HPV) testing for primary cervical cancer (CC) screening because of its high sensitivity. However, triage is desirable to correctly identify HPV+ women who have high-grade lesions (CIN2+) and require treatment. The ANRS-12375 study was conducted in Côte d'Ivoire, Burkina Faso and Cambodia to assess the performance, feasibility and benefits of different triage options for detecting CIN2+ lesions: partial (HPV16 and HPV16/18/45) and extended genotyping, visual inspection (VIA) alone and VIA combined with partial genotyping. VIA was performed by gynecologists. The sensitivity, specificity, and diagnostic likelihood ratio (DLR) of each triage option for detecting CIN2+ lesions with histology as a reference standard were calculated. Of the 2253 women living with HIV (WLHIV) included, 932 (41%) were HPV+. A CIN2+ lesion was identified in 105 (13%) of the 777 participants with histopathology results. The sensitivity of VIA as a triage test for CIN2+ patients was 89%, while that for extended genotyping was 89%, that for HPV16/18/45 partial genotyping was 51%, and that for HPV16 partial genotyping was 36%. The specificities for these tests were 45%, 29%, 72%., and 85%, respectively. Combining VIA and/or partial genotyping positivity slightly increased the sensitivity (94%) at the cost of lower specificity (28%). There was significant intersite heterogeneity (p = .04). Among the three triage tests with a sensitivity ≥85%, the VIA had the highest specificity and positive likelihood ratio (p < .001). VIA and extended genotyping, whether independent or combined, are good triage options with high sensitivity for identifying WLHIV needing treatment for CIN2+.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/us/*
dc.subject.enHIV
dc.subject.enHPV
dc.subject.enCervical Cancer
dc.subject.enResource‐Limited Countries
dc.subject.enScreening
dc.title.enPerformance of visual inspection, partial genotyping, and their combination for the triage of women living with HIV who are screen positive for human papillomavirus: Results from the AIMA-CC ANRS 12375 multicentric screening study
dc.title.alternativeInt J Canceren_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1002/ijc.35190en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed39319557en_US
bordeaux.journalInternational Journal of Canceren_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamGHIGS_BPHen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.identifier.funderIDAgence Nationale de Recherches sur le Sida et les Hépatites Viralesen_US
bordeaux.identifier.funderIDInstitut de Recherche pour le Développementen_US
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=International%20Journal%20of%20Cancer&amp;rft.date=2024-09-25&amp;rft.eissn=0020-7136&amp;rft.issn=0020-7136&amp;rft.au=DEBEAUDRAP,%20Pierre&amp;KABORE,%20Firmin%20Nongodo&amp;SETHA,%20Limsreng&amp;TEGBE,%20Joseph&amp;DOUKOURE,%20Brahima&amp;rft.genre=article


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