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Triaging HPV-positive women with p16/Ki-67 dual-stained cytology: Results from a sub-study nested into the ATHENA trial
Abstract Objectives In addition to genotyping for HPV16/18, dual-immunostaining for p16/Ki-67 has shown promise as a triage of HPV-positive women. We assessed the performance of p16/Ki-67 dual-stained cytology for triaging HPV-positive women undergoing primary HPV screening. Methods All women ≥ 25 y...
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Published in: | Gynecologic oncology 2017-01, Vol.144 (1), p.51-56 |
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description | Abstract Objectives In addition to genotyping for HPV16/18, dual-immunostaining for p16/Ki-67 has shown promise as a triage of HPV-positive women. We assessed the performance of p16/Ki-67 dual-stained cytology for triaging HPV-positive women undergoing primary HPV screening. Methods All women ≥ 25 years with valid cervical biopsy and cobas® HPV Test results from the cross-sectional phase of ATHENA who were referred to colposcopy (n = 7727) were eligible for enrolment. p16/Ki-67 dual-stained cytology was retrospectively performed on residual cytologic material collected into a second liquid-based cytology vial during the ATHENA enrolment visit. The diagnostic performance of dual-stained cytology, with or without HPV16/18 genotyping, for the detection of biopsy-confirmed cervical intraepithelial neoplasia grade 3 or worse (CIN3+) was determined and compared to Pap cytology. Furthermore, the number of colposcopies required per CIN3+ detected was determined. Results Dual-stained cytology was significantly more sensitive than Pap cytology (74.9% vs. 51.9%; p < 0.0001) for triaging HPV-positive women, whereas specificity was comparable (74.1% vs. 75.0%; p = 0.3198). Referral of all HPV16/18 positive women combined with dual-stained cytology triage of women positive for 12 “other” HPV genotypes provided the highest sensitivity for CIN3+ (86.8%; 95% CI: 81.9–90.8). A similar strategy but using Pap cytology for the triage of women positive for 12 “other” HPV genotypes was less sensitive (78.2%; 95% CI: 72.5–83.2; p = 0.0003), but required a similar number of colposcopies per CIN3+ detected. Conclusions p16/Ki-67 dual-stained cytology, either alone or combined with HPV16/18 genotyping, represents a promising approach as a sensitive and efficient triage for colposcopy of HPV-positive women when primary HPV screening is utilized. |
doi_str_mv | 10.1016/j.ygyno.2016.10.031 |
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We assessed the performance of p16/Ki-67 dual-stained cytology for triaging HPV-positive women undergoing primary HPV screening. Methods All women ≥ 25 years with valid cervical biopsy and cobas® HPV Test results from the cross-sectional phase of ATHENA who were referred to colposcopy (n = 7727) were eligible for enrolment. p16/Ki-67 dual-stained cytology was retrospectively performed on residual cytologic material collected into a second liquid-based cytology vial during the ATHENA enrolment visit. The diagnostic performance of dual-stained cytology, with or without HPV16/18 genotyping, for the detection of biopsy-confirmed cervical intraepithelial neoplasia grade 3 or worse (CIN3+) was determined and compared to Pap cytology. Furthermore, the number of colposcopies required per CIN3+ detected was determined. Results Dual-stained cytology was significantly more sensitive than Pap cytology (74.9% vs. 51.9%; p < 0.0001) for triaging HPV-positive women, whereas specificity was comparable (74.1% vs. 75.0%; p = 0.3198). Referral of all HPV16/18 positive women combined with dual-stained cytology triage of women positive for 12 “other” HPV genotypes provided the highest sensitivity for CIN3+ (86.8%; 95% CI: 81.9–90.8). A similar strategy but using Pap cytology for the triage of women positive for 12 “other” HPV genotypes was less sensitive (78.2%; 95% CI: 72.5–83.2; p = 0.0003), but required a similar number of colposcopies per CIN3+ detected. Conclusions p16/Ki-67 dual-stained cytology, either alone or combined with HPV16/18 genotyping, represents a promising approach as a sensitive and efficient triage for colposcopy of HPV-positive women when primary HPV screening is utilized.</description><identifier>ISSN: 0090-8258</identifier><identifier>EISSN: 1095-6859</identifier><identifier>DOI: 10.1016/j.ygyno.2016.10.031</identifier><identifier>PMID: 28094038</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; ATHENA ; Biopsy ; Cervical cancer screening ; Cervical Intraepithelial Neoplasia - chemistry ; Cervical Intraepithelial Neoplasia - diagnosis ; Cervical Intraepithelial Neoplasia - pathology ; Cervical Intraepithelial Neoplasia - virology ; Cervix Uteri - pathology ; CINtec PLUS ; Clinical Trials as Topic ; Colposcopy ; Cyclin-Dependent Kinase Inhibitor p16 - analysis ; Female ; Genotype ; Genotyping ; Hematology, Oncology and Palliative Medicine ; HPV ; Humans ; Ki-67 Antigen - analysis ; Obstetrics and Gynecology ; p16/Ki-67 dual-stained cytology ; Papanicolaou Test ; Papillomaviridae - genetics ; Papillomavirus Infections - diagnosis ; Papillomavirus Infections - virology ; Predictive Value of Tests ; Referral and Consultation ; Retrospective Studies ; Triage ; Triage - methods ; Uterine Cervical Neoplasms - chemistry ; Uterine Cervical Neoplasms - diagnosis ; Uterine Cervical Neoplasms - pathology ; Uterine Cervical Neoplasms - virology ; Vaginal Smears</subject><ispartof>Gynecologic oncology, 2017-01, Vol.144 (1), p.51-56</ispartof><rights>2016</rights><rights>Copyright © 2016. Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c414t-85f2816e87498aa088f4a68107eb9893f6d21bcfe7f37593baa2c3a67078aa013</citedby><cites>FETCH-LOGICAL-c414t-85f2816e87498aa088f4a68107eb9893f6d21bcfe7f37593baa2c3a67078aa013</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28094038$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wright, Thomas C</creatorcontrib><creatorcontrib>Behrens, Catherine M</creatorcontrib><creatorcontrib>Ranger-Moore, James</creatorcontrib><creatorcontrib>Rehm, Susanne</creatorcontrib><creatorcontrib>Sharma, Abha</creatorcontrib><creatorcontrib>Stoler, Mark H</creatorcontrib><creatorcontrib>Ridder, Ruediger</creatorcontrib><title>Triaging HPV-positive women with p16/Ki-67 dual-stained cytology: Results from a sub-study nested into the ATHENA trial</title><title>Gynecologic oncology</title><addtitle>Gynecol Oncol</addtitle><description>Abstract Objectives In addition to genotyping for HPV16/18, dual-immunostaining for p16/Ki-67 has shown promise as a triage of HPV-positive women. We assessed the performance of p16/Ki-67 dual-stained cytology for triaging HPV-positive women undergoing primary HPV screening. Methods All women ≥ 25 years with valid cervical biopsy and cobas® HPV Test results from the cross-sectional phase of ATHENA who were referred to colposcopy (n = 7727) were eligible for enrolment. p16/Ki-67 dual-stained cytology was retrospectively performed on residual cytologic material collected into a second liquid-based cytology vial during the ATHENA enrolment visit. The diagnostic performance of dual-stained cytology, with or without HPV16/18 genotyping, for the detection of biopsy-confirmed cervical intraepithelial neoplasia grade 3 or worse (CIN3+) was determined and compared to Pap cytology. Furthermore, the number of colposcopies required per CIN3+ detected was determined. Results Dual-stained cytology was significantly more sensitive than Pap cytology (74.9% vs. 51.9%; p < 0.0001) for triaging HPV-positive women, whereas specificity was comparable (74.1% vs. 75.0%; p = 0.3198). Referral of all HPV16/18 positive women combined with dual-stained cytology triage of women positive for 12 “other” HPV genotypes provided the highest sensitivity for CIN3+ (86.8%; 95% CI: 81.9–90.8). A similar strategy but using Pap cytology for the triage of women positive for 12 “other” HPV genotypes was less sensitive (78.2%; 95% CI: 72.5–83.2; p = 0.0003), but required a similar number of colposcopies per CIN3+ detected. Conclusions p16/Ki-67 dual-stained cytology, either alone or combined with HPV16/18 genotyping, represents a promising approach as a sensitive and efficient triage for colposcopy of HPV-positive women when primary HPV screening is utilized.</description><subject>Adult</subject><subject>ATHENA</subject><subject>Biopsy</subject><subject>Cervical cancer screening</subject><subject>Cervical Intraepithelial Neoplasia - chemistry</subject><subject>Cervical Intraepithelial Neoplasia - diagnosis</subject><subject>Cervical Intraepithelial Neoplasia - pathology</subject><subject>Cervical Intraepithelial Neoplasia - virology</subject><subject>Cervix Uteri - pathology</subject><subject>CINtec PLUS</subject><subject>Clinical Trials as Topic</subject><subject>Colposcopy</subject><subject>Cyclin-Dependent Kinase Inhibitor p16 - analysis</subject><subject>Female</subject><subject>Genotype</subject><subject>Genotyping</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>HPV</subject><subject>Humans</subject><subject>Ki-67 Antigen - analysis</subject><subject>Obstetrics and Gynecology</subject><subject>p16/Ki-67 dual-stained cytology</subject><subject>Papanicolaou Test</subject><subject>Papillomaviridae - genetics</subject><subject>Papillomavirus Infections - diagnosis</subject><subject>Papillomavirus Infections - virology</subject><subject>Predictive Value of Tests</subject><subject>Referral and Consultation</subject><subject>Retrospective Studies</subject><subject>Triage</subject><subject>Triage - methods</subject><subject>Uterine Cervical Neoplasms - chemistry</subject><subject>Uterine Cervical Neoplasms - diagnosis</subject><subject>Uterine Cervical Neoplasms - pathology</subject><subject>Uterine Cervical Neoplasms - virology</subject><subject>Vaginal Smears</subject><issn>0090-8258</issn><issn>1095-6859</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqFkcFu1DAQhi0EokvhCZCQj1yy2HHiOEggrarSrVoVBAtXy3EmWy-JvbWdrvL2ddjCgUtPlkff-B9_g9BbSpaUUP5ht5y2k3XLPF1SZUkYfYYWlNRlxkVZP0cLQmqSibwUJ-hVCDtCCCM0f4lOckHqgjCxQIeNN2pr7Bavv_3K9i6YaO4BH9wAFh9MvMX7FHVlMl7hdlR9FqIyFlqsp-h6t50-4u8Qxj4G3Hk3YIXD2CRobCdsIcREGhsdjreAV5v1-c0Kx5TYv0YvOtUHePN4nqKfX843Z-vs-uvF5dnqOtMFLWImyi4XlIOoilooRYToCsUFJRU0tahZx9ucNrqDqmNVWbNGqVwzxStSzThlp-j98d29d3djGkgOJmjoe2XBjUFSwWlZFkVVJ5QdUe1dCB46ufdmUH6SlMjZuNzJP8blbHwuJuOp691jwNgM0P7r-as4AZ-OAKRv3hvwMmgDVkNrPOgoW2eeCPj8X7_ujTVa9b9hgrBzo7fJoKQy5JLIH_PS551TzmhJBGcPeaunJw</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Wright, Thomas C</creator><creator>Behrens, Catherine M</creator><creator>Ranger-Moore, James</creator><creator>Rehm, Susanne</creator><creator>Sharma, Abha</creator><creator>Stoler, Mark H</creator><creator>Ridder, Ruediger</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20170101</creationdate><title>Triaging HPV-positive women with p16/Ki-67 dual-stained cytology: Results from a sub-study nested into the ATHENA trial</title><author>Wright, Thomas C ; Behrens, Catherine M ; Ranger-Moore, James ; Rehm, Susanne ; Sharma, Abha ; Stoler, Mark H ; Ridder, Ruediger</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c414t-85f2816e87498aa088f4a68107eb9893f6d21bcfe7f37593baa2c3a67078aa013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>ATHENA</topic><topic>Biopsy</topic><topic>Cervical cancer screening</topic><topic>Cervical Intraepithelial Neoplasia - chemistry</topic><topic>Cervical Intraepithelial Neoplasia - diagnosis</topic><topic>Cervical Intraepithelial Neoplasia - pathology</topic><topic>Cervical Intraepithelial Neoplasia - virology</topic><topic>Cervix Uteri - pathology</topic><topic>CINtec PLUS</topic><topic>Clinical Trials as Topic</topic><topic>Colposcopy</topic><topic>Cyclin-Dependent Kinase Inhibitor p16 - analysis</topic><topic>Female</topic><topic>Genotype</topic><topic>Genotyping</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>HPV</topic><topic>Humans</topic><topic>Ki-67 Antigen - analysis</topic><topic>Obstetrics and Gynecology</topic><topic>p16/Ki-67 dual-stained cytology</topic><topic>Papanicolaou Test</topic><topic>Papillomaviridae - genetics</topic><topic>Papillomavirus Infections - diagnosis</topic><topic>Papillomavirus Infections - virology</topic><topic>Predictive Value of Tests</topic><topic>Referral and Consultation</topic><topic>Retrospective Studies</topic><topic>Triage</topic><topic>Triage - methods</topic><topic>Uterine Cervical Neoplasms - chemistry</topic><topic>Uterine Cervical Neoplasms - diagnosis</topic><topic>Uterine Cervical Neoplasms - pathology</topic><topic>Uterine Cervical Neoplasms - virology</topic><topic>Vaginal Smears</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wright, Thomas C</creatorcontrib><creatorcontrib>Behrens, Catherine M</creatorcontrib><creatorcontrib>Ranger-Moore, James</creatorcontrib><creatorcontrib>Rehm, Susanne</creatorcontrib><creatorcontrib>Sharma, Abha</creatorcontrib><creatorcontrib>Stoler, Mark H</creatorcontrib><creatorcontrib>Ridder, Ruediger</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><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>Wright, Thomas C</au><au>Behrens, Catherine M</au><au>Ranger-Moore, James</au><au>Rehm, Susanne</au><au>Sharma, Abha</au><au>Stoler, Mark H</au><au>Ridder, Ruediger</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Triaging HPV-positive women with p16/Ki-67 dual-stained cytology: Results from a sub-study nested into the ATHENA trial</atitle><jtitle>Gynecologic oncology</jtitle><addtitle>Gynecol Oncol</addtitle><date>2017-01-01</date><risdate>2017</risdate><volume>144</volume><issue>1</issue><spage>51</spage><epage>56</epage><pages>51-56</pages><issn>0090-8258</issn><eissn>1095-6859</eissn><abstract>Abstract Objectives In addition to genotyping for HPV16/18, dual-immunostaining for p16/Ki-67 has shown promise as a triage of HPV-positive women. We assessed the performance of p16/Ki-67 dual-stained cytology for triaging HPV-positive women undergoing primary HPV screening. Methods All women ≥ 25 years with valid cervical biopsy and cobas® HPV Test results from the cross-sectional phase of ATHENA who were referred to colposcopy (n = 7727) were eligible for enrolment. p16/Ki-67 dual-stained cytology was retrospectively performed on residual cytologic material collected into a second liquid-based cytology vial during the ATHENA enrolment visit. The diagnostic performance of dual-stained cytology, with or without HPV16/18 genotyping, for the detection of biopsy-confirmed cervical intraepithelial neoplasia grade 3 or worse (CIN3+) was determined and compared to Pap cytology. Furthermore, the number of colposcopies required per CIN3+ detected was determined. Results Dual-stained cytology was significantly more sensitive than Pap cytology (74.9% vs. 51.9%; p < 0.0001) for triaging HPV-positive women, whereas specificity was comparable (74.1% vs. 75.0%; p = 0.3198). Referral of all HPV16/18 positive women combined with dual-stained cytology triage of women positive for 12 “other” HPV genotypes provided the highest sensitivity for CIN3+ (86.8%; 95% CI: 81.9–90.8). A similar strategy but using Pap cytology for the triage of women positive for 12 “other” HPV genotypes was less sensitive (78.2%; 95% CI: 72.5–83.2; p = 0.0003), but required a similar number of colposcopies per CIN3+ detected. Conclusions p16/Ki-67 dual-stained cytology, either alone or combined with HPV16/18 genotyping, represents a promising approach as a sensitive and efficient triage for colposcopy of HPV-positive women when primary HPV screening is utilized.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28094038</pmid><doi>10.1016/j.ygyno.2016.10.031</doi><tpages>6</tpages></addata></record> |
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subjects | Adult ATHENA Biopsy Cervical cancer screening Cervical Intraepithelial Neoplasia - chemistry Cervical Intraepithelial Neoplasia - diagnosis Cervical Intraepithelial Neoplasia - pathology Cervical Intraepithelial Neoplasia - virology Cervix Uteri - pathology CINtec PLUS Clinical Trials as Topic Colposcopy Cyclin-Dependent Kinase Inhibitor p16 - analysis Female Genotype Genotyping Hematology, Oncology and Palliative Medicine HPV Humans Ki-67 Antigen - analysis Obstetrics and Gynecology p16/Ki-67 dual-stained cytology Papanicolaou Test Papillomaviridae - genetics Papillomavirus Infections - diagnosis Papillomavirus Infections - virology Predictive Value of Tests Referral and Consultation Retrospective Studies Triage Triage - methods Uterine Cervical Neoplasms - chemistry Uterine Cervical Neoplasms - diagnosis Uterine Cervical Neoplasms - pathology Uterine Cervical Neoplasms - virology Vaginal Smears |
title | Triaging HPV-positive women with p16/Ki-67 dual-stained cytology: Results from a sub-study nested into the ATHENA trial |
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