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Screening for cervical cancer among HIV-positive and HIV-negative women in Cameroon using simultaneous co-testing with careHPV DNA testing and visual inspection enhanced by digital cervicography: Findings of initial screening and one-year follow-up
The World Health Organization (WHO)'s cervical cancer screening guidelines for limited-resource settings recommend sequential screening followed by same-day treatment under a “screen-and-treat” approach. We aimed to (1) assess feasibility and clinical outcomes of screening HIV-positive and HIV-...
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Published in: | Gynecologic oncology 2018-01, Vol.148 (1), p.118-125 |
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creator | Cholli, Preetam Bradford, Leslie Manga, Simon Nulah, Kathleen Kiyang, Edith Manjuh, Florence DeGregorio, Geneva Ogembo, Rebecca K. Orock, Enow Liu, Yuxin Wamai, Richard G. Sheldon, Lisa Kennedy Gona, Philimon N. Sando, Zacharie Welty, Thomas Welty, Edith Ogembo, Javier Gordon |
description | The World Health Organization (WHO)'s cervical cancer screening guidelines for limited-resource settings recommend sequential screening followed by same-day treatment under a “screen-and-treat” approach. We aimed to (1) assess feasibility and clinical outcomes of screening HIV-positive and HIV-negative Cameroonian women by pairing visual inspection with acetic acid and Lugol's iodine enhanced by digital cervicography (VIA/VILI-DC) with careHPV, a high-risk human papillomavirus (HR-HPV) nucleic acid test designed for low-resource settings; and (2) determine persistence of HR-HPV infection after one-year follow-up to inform optimal screening, treatment, and follow-up algorithms.
We co-tested 913 previously unscreened women aged ≥30years and applied WHO-recommended treatment for all VIA/VILI-DC-positive women. Baseline prevalence of HR-HPV and HIV were 24% and 42%, respectively.
On initial screen, 44 (5%) women were VIA/VILI-DC-positive, of whom 22 had HR-HPV infection, indicating 50% of women screened false-positive and would have been triaged for unnecessary same-day treatment. VIA/VILI-DC-positive women with HIV infection were three times more likely to be HR-HPV-positive than HIV-negative women (65% vs. 20%). All women positive for either VIA/VILI-DC or HR-HPV (n=245) were invited for repeat co-testing after one year, of which 136 (56%) returned for follow-up. Of 122 women who were HR-HPV-positive on initial screen, 60 (49%) re-tested negative, of whom 6 had received treatment after initial screen, indicating that 44% of initially HR-HPV-positive women spontaneously cleared infection after one year without treatment. Women with HIV were more likely to remain HR-HPV-positive on follow-up than HIV-negative women (61% vs. 22%, p |
doi_str_mv | 10.1016/j.ygyno.2017.11.002 |
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We co-tested 913 previously unscreened women aged ≥30years and applied WHO-recommended treatment for all VIA/VILI-DC-positive women. Baseline prevalence of HR-HPV and HIV were 24% and 42%, respectively.
On initial screen, 44 (5%) women were VIA/VILI-DC-positive, of whom 22 had HR-HPV infection, indicating 50% of women screened false-positive and would have been triaged for unnecessary same-day treatment. VIA/VILI-DC-positive women with HIV infection were three times more likely to be HR-HPV-positive than HIV-negative women (65% vs. 20%). All women positive for either VIA/VILI-DC or HR-HPV (n=245) were invited for repeat co-testing after one year, of which 136 (56%) returned for follow-up. Of 122 women who were HR-HPV-positive on initial screen, 60 (49%) re-tested negative, of whom 6 had received treatment after initial screen, indicating that 44% of initially HR-HPV-positive women spontaneously cleared infection after one year without treatment. Women with HIV were more likely to remain HR-HPV-positive on follow-up than HIV-negative women (61% vs. 22%, p<0.001). Treatment was offered to all VIA/VILI-DC positive women on initial screen, and to all women screening VIA/VILI-DC or HR-HPV positive on follow-up.
We found careHPV co-testing with VIA/VILI-DC to be feasible and valuable in identifying false-positives, but careHPV screening-to-result time was too long to inform same-day treatment.
•Co-testing for cervical cancer and its precursors in resource-limited settings.•Half of all VIA/VILI-DC positive women had no associated high risk HPV infection.•VIA/VILI-DC false positives dropped from 50% overall to 14% in HIV-positive women•Nearly half (44.3%) of all HPV-positive women spontaneously cleared infection in one year•HPV co-testing with VIA/VILI-DC may identify false positives, reduce overtreatment</description><identifier>ISSN: 0090-8258</identifier><identifier>EISSN: 1095-6859</identifier><identifier>DOI: 10.1016/j.ygyno.2017.11.002</identifier><identifier>PMID: 29153541</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Cervical cancer screening ; HPV DNA testing ; Sub-Saharan Africa ; Visual inspection with acetic acid ; Women's health</subject><ispartof>Gynecologic oncology, 2018-01, Vol.148 (1), p.118-125</ispartof><rights>2017 Elsevier Inc.</rights><rights>Copyright © 2017 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-22f070f42d9f4640a8c7c6bab2d76f7320c2340e0c195cd63e9c40fe3b93d3693</citedby><cites>FETCH-LOGICAL-c359t-22f070f42d9f4640a8c7c6bab2d76f7320c2340e0c195cd63e9c40fe3b93d3693</cites><orcidid>0000-0001-6949-8693 ; 0000-0002-3701-4575</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29153541$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cholli, Preetam</creatorcontrib><creatorcontrib>Bradford, Leslie</creatorcontrib><creatorcontrib>Manga, Simon</creatorcontrib><creatorcontrib>Nulah, Kathleen</creatorcontrib><creatorcontrib>Kiyang, Edith</creatorcontrib><creatorcontrib>Manjuh, Florence</creatorcontrib><creatorcontrib>DeGregorio, Geneva</creatorcontrib><creatorcontrib>Ogembo, Rebecca K.</creatorcontrib><creatorcontrib>Orock, Enow</creatorcontrib><creatorcontrib>Liu, Yuxin</creatorcontrib><creatorcontrib>Wamai, Richard G.</creatorcontrib><creatorcontrib>Sheldon, Lisa Kennedy</creatorcontrib><creatorcontrib>Gona, Philimon N.</creatorcontrib><creatorcontrib>Sando, Zacharie</creatorcontrib><creatorcontrib>Welty, Thomas</creatorcontrib><creatorcontrib>Welty, Edith</creatorcontrib><creatorcontrib>Ogembo, Javier Gordon</creatorcontrib><title>Screening for cervical cancer among HIV-positive and HIV-negative women in Cameroon using simultaneous co-testing with careHPV DNA testing and visual inspection enhanced by digital cervicography: Findings of initial screening and one-year follow-up</title><title>Gynecologic oncology</title><addtitle>Gynecol Oncol</addtitle><description>The World Health Organization (WHO)'s cervical cancer screening guidelines for limited-resource settings recommend sequential screening followed by same-day treatment under a “screen-and-treat” approach. We aimed to (1) assess feasibility and clinical outcomes of screening HIV-positive and HIV-negative Cameroonian women by pairing visual inspection with acetic acid and Lugol's iodine enhanced by digital cervicography (VIA/VILI-DC) with careHPV, a high-risk human papillomavirus (HR-HPV) nucleic acid test designed for low-resource settings; and (2) determine persistence of HR-HPV infection after one-year follow-up to inform optimal screening, treatment, and follow-up algorithms.
We co-tested 913 previously unscreened women aged ≥30years and applied WHO-recommended treatment for all VIA/VILI-DC-positive women. Baseline prevalence of HR-HPV and HIV were 24% and 42%, respectively.
On initial screen, 44 (5%) women were VIA/VILI-DC-positive, of whom 22 had HR-HPV infection, indicating 50% of women screened false-positive and would have been triaged for unnecessary same-day treatment. VIA/VILI-DC-positive women with HIV infection were three times more likely to be HR-HPV-positive than HIV-negative women (65% vs. 20%). All women positive for either VIA/VILI-DC or HR-HPV (n=245) were invited for repeat co-testing after one year, of which 136 (56%) returned for follow-up. Of 122 women who were HR-HPV-positive on initial screen, 60 (49%) re-tested negative, of whom 6 had received treatment after initial screen, indicating that 44% of initially HR-HPV-positive women spontaneously cleared infection after one year without treatment. Women with HIV were more likely to remain HR-HPV-positive on follow-up than HIV-negative women (61% vs. 22%, p<0.001). Treatment was offered to all VIA/VILI-DC positive women on initial screen, and to all women screening VIA/VILI-DC or HR-HPV positive on follow-up.
We found careHPV co-testing with VIA/VILI-DC to be feasible and valuable in identifying false-positives, but careHPV screening-to-result time was too long to inform same-day treatment.
•Co-testing for cervical cancer and its precursors in resource-limited settings.•Half of all VIA/VILI-DC positive women had no associated high risk HPV infection.•VIA/VILI-DC false positives dropped from 50% overall to 14% in HIV-positive women•Nearly half (44.3%) of all HPV-positive women spontaneously cleared infection in one year•HPV co-testing with VIA/VILI-DC may identify false positives, reduce overtreatment</description><subject>Cervical cancer screening</subject><subject>HPV DNA testing</subject><subject>Sub-Saharan Africa</subject><subject>Visual inspection with acetic acid</subject><subject>Women's health</subject><issn>0090-8258</issn><issn>1095-6859</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9UcGO0zAQjRCILQtfgIR85JIwtpO0RuKwKux2pRUgAXu1HGfSukrsYCet8ucc12l398jJ1sybN-_NS5L3FDIKtPy0z6btZF3GgC4zSjMA9iJZUBBFWq4K8TJZAAhIV6xYXSRvQtgDAAfKXicXTNCCFzldJP9-aY9ojd2Sxnmi0R-MVi3RysY_UZ2Lnc3tfdq7YAZzQKJsfSpY3KpT4eg6tMRYslYdeucsGcPMF0w3toOy6MZAtEsHDMNcP5phF_k9bn7ek6_fr8hTY2Y-mDDG9caGHvVgIhna3aylJtVEarM1w6zuJNNtvep302dybWwdCQJxTZyMMiMkPPuaaZ3FdELlo8m2dcd07N8mrxrVBnz3-F4mf66__V5v0rsfN7frq7tU80IMKWMNLKHJWS2avMxBrfRSl5WqWL0smyVnoBnPAUFTUei65Ch0Dg3ySvCal4JfJh_PvL13f8foVHYmaGzb82EkFWWZ5wIKiFB-hmrvQvDYyN6bTvlJUpBz5HIvT5HLOXJJqYyRx6kPjwvGqsP6eeYp4wj4cgZgtHkw6GXQBueTGh9vLGtn_rvgAQvExEI</recordid><startdate>201801</startdate><enddate>201801</enddate><creator>Cholli, Preetam</creator><creator>Bradford, Leslie</creator><creator>Manga, Simon</creator><creator>Nulah, Kathleen</creator><creator>Kiyang, Edith</creator><creator>Manjuh, Florence</creator><creator>DeGregorio, Geneva</creator><creator>Ogembo, Rebecca K.</creator><creator>Orock, Enow</creator><creator>Liu, Yuxin</creator><creator>Wamai, Richard G.</creator><creator>Sheldon, Lisa Kennedy</creator><creator>Gona, Philimon N.</creator><creator>Sando, Zacharie</creator><creator>Welty, Thomas</creator><creator>Welty, Edith</creator><creator>Ogembo, Javier Gordon</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6949-8693</orcidid><orcidid>https://orcid.org/0000-0002-3701-4575</orcidid></search><sort><creationdate>201801</creationdate><title>Screening for cervical cancer among HIV-positive and HIV-negative women in Cameroon using simultaneous co-testing with careHPV DNA testing and visual inspection enhanced by digital cervicography: Findings of initial screening and one-year follow-up</title><author>Cholli, Preetam ; Bradford, Leslie ; Manga, Simon ; Nulah, Kathleen ; Kiyang, Edith ; Manjuh, Florence ; DeGregorio, Geneva ; Ogembo, Rebecca K. ; Orock, Enow ; Liu, Yuxin ; Wamai, Richard G. ; Sheldon, Lisa Kennedy ; Gona, Philimon N. ; Sando, Zacharie ; Welty, Thomas ; Welty, Edith ; Ogembo, Javier Gordon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-22f070f42d9f4640a8c7c6bab2d76f7320c2340e0c195cd63e9c40fe3b93d3693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Cervical cancer screening</topic><topic>HPV DNA testing</topic><topic>Sub-Saharan Africa</topic><topic>Visual inspection with acetic acid</topic><topic>Women's health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cholli, Preetam</creatorcontrib><creatorcontrib>Bradford, Leslie</creatorcontrib><creatorcontrib>Manga, Simon</creatorcontrib><creatorcontrib>Nulah, Kathleen</creatorcontrib><creatorcontrib>Kiyang, Edith</creatorcontrib><creatorcontrib>Manjuh, Florence</creatorcontrib><creatorcontrib>DeGregorio, Geneva</creatorcontrib><creatorcontrib>Ogembo, Rebecca K.</creatorcontrib><creatorcontrib>Orock, Enow</creatorcontrib><creatorcontrib>Liu, Yuxin</creatorcontrib><creatorcontrib>Wamai, Richard G.</creatorcontrib><creatorcontrib>Sheldon, Lisa Kennedy</creatorcontrib><creatorcontrib>Gona, Philimon N.</creatorcontrib><creatorcontrib>Sando, Zacharie</creatorcontrib><creatorcontrib>Welty, Thomas</creatorcontrib><creatorcontrib>Welty, Edith</creatorcontrib><creatorcontrib>Ogembo, Javier Gordon</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Gynecologic oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cholli, Preetam</au><au>Bradford, Leslie</au><au>Manga, Simon</au><au>Nulah, Kathleen</au><au>Kiyang, Edith</au><au>Manjuh, Florence</au><au>DeGregorio, Geneva</au><au>Ogembo, Rebecca K.</au><au>Orock, Enow</au><au>Liu, Yuxin</au><au>Wamai, Richard G.</au><au>Sheldon, Lisa Kennedy</au><au>Gona, Philimon N.</au><au>Sando, Zacharie</au><au>Welty, Thomas</au><au>Welty, Edith</au><au>Ogembo, Javier Gordon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Screening for cervical cancer among HIV-positive and HIV-negative women in Cameroon using simultaneous co-testing with careHPV DNA testing and visual inspection enhanced by digital cervicography: Findings of initial screening and one-year follow-up</atitle><jtitle>Gynecologic oncology</jtitle><addtitle>Gynecol Oncol</addtitle><date>2018-01</date><risdate>2018</risdate><volume>148</volume><issue>1</issue><spage>118</spage><epage>125</epage><pages>118-125</pages><issn>0090-8258</issn><eissn>1095-6859</eissn><abstract>The World Health Organization (WHO)'s cervical cancer screening guidelines for limited-resource settings recommend sequential screening followed by same-day treatment under a “screen-and-treat” approach. We aimed to (1) assess feasibility and clinical outcomes of screening HIV-positive and HIV-negative Cameroonian women by pairing visual inspection with acetic acid and Lugol's iodine enhanced by digital cervicography (VIA/VILI-DC) with careHPV, a high-risk human papillomavirus (HR-HPV) nucleic acid test designed for low-resource settings; and (2) determine persistence of HR-HPV infection after one-year follow-up to inform optimal screening, treatment, and follow-up algorithms.
We co-tested 913 previously unscreened women aged ≥30years and applied WHO-recommended treatment for all VIA/VILI-DC-positive women. Baseline prevalence of HR-HPV and HIV were 24% and 42%, respectively.
On initial screen, 44 (5%) women were VIA/VILI-DC-positive, of whom 22 had HR-HPV infection, indicating 50% of women screened false-positive and would have been triaged for unnecessary same-day treatment. VIA/VILI-DC-positive women with HIV infection were three times more likely to be HR-HPV-positive than HIV-negative women (65% vs. 20%). All women positive for either VIA/VILI-DC or HR-HPV (n=245) were invited for repeat co-testing after one year, of which 136 (56%) returned for follow-up. Of 122 women who were HR-HPV-positive on initial screen, 60 (49%) re-tested negative, of whom 6 had received treatment after initial screen, indicating that 44% of initially HR-HPV-positive women spontaneously cleared infection after one year without treatment. Women with HIV were more likely to remain HR-HPV-positive on follow-up than HIV-negative women (61% vs. 22%, p<0.001). Treatment was offered to all VIA/VILI-DC positive women on initial screen, and to all women screening VIA/VILI-DC or HR-HPV positive on follow-up.
We found careHPV co-testing with VIA/VILI-DC to be feasible and valuable in identifying false-positives, but careHPV screening-to-result time was too long to inform same-day treatment.
•Co-testing for cervical cancer and its precursors in resource-limited settings.•Half of all VIA/VILI-DC positive women had no associated high risk HPV infection.•VIA/VILI-DC false positives dropped from 50% overall to 14% in HIV-positive women•Nearly half (44.3%) of all HPV-positive women spontaneously cleared infection in one year•HPV co-testing with VIA/VILI-DC may identify false positives, reduce overtreatment</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>29153541</pmid><doi>10.1016/j.ygyno.2017.11.002</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-6949-8693</orcidid><orcidid>https://orcid.org/0000-0002-3701-4575</orcidid></addata></record> |
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subjects | Cervical cancer screening HPV DNA testing Sub-Saharan Africa Visual inspection with acetic acid Women's health |
title | Screening for cervical cancer among HIV-positive and HIV-negative women in Cameroon using simultaneous co-testing with careHPV DNA testing and visual inspection enhanced by digital cervicography: Findings of initial screening and one-year follow-up |
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