Self-collection for high-risk HPV detection in Brazilian women using the care HPV™ test

Detalhes bibliográficos
Autor(a) principal: Lorenzi, Adriana Tarlá
Data de Publicação: 2013
Outros Autores: Fregnani, José Humberto, Possati-Resende, Júlio César, Neto, Cristovam Scapulatempo, Villa, Luisa Lina, Longatto Filho, Adhemar
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/25221
Resumo: Cervical cancer is the second most common cancer among Brazilian women. High-risk human papillomavirus (hr-HPV) persistence is the primary cause of cervical neoplasia. Early detection of hr-HPV is important for identifying women at risk for developing cervical lesions. Approximately 85% of new cases of cervical cancer worldwide and 50% of the total cervical cancer deaths occurred in developing countries. Here, a new methodology to support a cervical cancer screening program was evaluated in women from various Brazilian regions. METHODS: Two thousand women aged 18-77years were enrolled in an opportunistic cervical cancer screening program and were randomized into self-vaginal or health professional-guided cervical sampling groups. The Qiagen careHPV™ test was performed on all samples. Pap tests were performed on all women using liquid-based cytology. RESULTS: Positive hr-HPV results were obtained in 12.3% (245/2000) of women; similar rates were observed in self- or health professional-collected samples. Eighty-nine percent (1719/2000) of cervical cytologies classified as normal were negative to hr-HPV. Among the cytological samples, 36.6% classified as ASC-US+ were positive to hr-HPV, 78.8% were LSIL and 75.0% were HSIL. CONCLUSIONS: Self-sampled and health professional-sampled vaginal/cervical specimens did not differ in their rates of detection of hr-HPV. Therefore, HPV DNA testing in self-sampled vaginal cells is an alternative to primary screening in low-resource settings.
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spelling Self-collection for high-risk HPV detection in Brazilian women using the care HPV™ testHuman papillomavirusCervical cancerSelf-samplingMolecular testScreeningScience & TechnologyCervical cancer is the second most common cancer among Brazilian women. High-risk human papillomavirus (hr-HPV) persistence is the primary cause of cervical neoplasia. Early detection of hr-HPV is important for identifying women at risk for developing cervical lesions. Approximately 85% of new cases of cervical cancer worldwide and 50% of the total cervical cancer deaths occurred in developing countries. Here, a new methodology to support a cervical cancer screening program was evaluated in women from various Brazilian regions. METHODS: Two thousand women aged 18-77years were enrolled in an opportunistic cervical cancer screening program and were randomized into self-vaginal or health professional-guided cervical sampling groups. The Qiagen careHPV™ test was performed on all samples. Pap tests were performed on all women using liquid-based cytology. RESULTS: Positive hr-HPV results were obtained in 12.3% (245/2000) of women; similar rates were observed in self- or health professional-collected samples. Eighty-nine percent (1719/2000) of cervical cytologies classified as normal were negative to hr-HPV. Among the cytological samples, 36.6% classified as ASC-US+ were positive to hr-HPV, 78.8% were LSIL and 75.0% were HSIL. CONCLUSIONS: Self-sampled and health professional-sampled vaginal/cervical specimens did not differ in their rates of detection of hr-HPV. Therefore, HPV DNA testing in self-sampled vaginal cells is an alternative to primary screening in low-resource settings.The authors thank the following: Cancer Prevention Department Team, Cleyton Zanardo de Oliveira and Allini Mafra of the Researcher Support Team and the Pathology Depai Intent of the Barretos Cancer Hospital. Rui Manuel Reis and Andre Lopes Carvalho from the Molecular Oncology Center; Jose Eduardo Levi from Sao Paulo University; Cintia B. Oliveira, Raphael Haikel junior and Edmundo Mauad from Barretos Cancer Hospital. Luisa Lina Villa was supported by a grant from CNPq and FAPESP (INCT-HPV). Study Supported by CNPq - Process no 573799/2008-3 and FAPESP no 2008/57889-1. They also thank all volunteer women who participated of this study.ElsevierUniversidade do MinhoLorenzi, Adriana TarláFregnani, José HumbertoPossati-Resende, Júlio CésarNeto, Cristovam ScapulatempoVilla, Luisa LinaLongatto Filho, Adhemar20132013-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/25221eng0090-825810.1016/j.ygyno.2013.07.09223880151www.journals.elsevier.com/gynecologic-oncology/?info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:54:03Zoai:repositorium.sdum.uminho.pt:1822/25221Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:53:35.075643Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Self-collection for high-risk HPV detection in Brazilian women using the care HPV™ test
title Self-collection for high-risk HPV detection in Brazilian women using the care HPV™ test
spellingShingle Self-collection for high-risk HPV detection in Brazilian women using the care HPV™ test
Lorenzi, Adriana Tarlá
Human papillomavirus
Cervical cancer
Self-sampling
Molecular test
Screening
Science & Technology
title_short Self-collection for high-risk HPV detection in Brazilian women using the care HPV™ test
title_full Self-collection for high-risk HPV detection in Brazilian women using the care HPV™ test
title_fullStr Self-collection for high-risk HPV detection in Brazilian women using the care HPV™ test
title_full_unstemmed Self-collection for high-risk HPV detection in Brazilian women using the care HPV™ test
title_sort Self-collection for high-risk HPV detection in Brazilian women using the care HPV™ test
author Lorenzi, Adriana Tarlá
author_facet Lorenzi, Adriana Tarlá
Fregnani, José Humberto
Possati-Resende, Júlio César
Neto, Cristovam Scapulatempo
Villa, Luisa Lina
Longatto Filho, Adhemar
author_role author
author2 Fregnani, José Humberto
Possati-Resende, Júlio César
Neto, Cristovam Scapulatempo
Villa, Luisa Lina
Longatto Filho, Adhemar
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Lorenzi, Adriana Tarlá
Fregnani, José Humberto
Possati-Resende, Júlio César
Neto, Cristovam Scapulatempo
Villa, Luisa Lina
Longatto Filho, Adhemar
dc.subject.por.fl_str_mv Human papillomavirus
Cervical cancer
Self-sampling
Molecular test
Screening
Science & Technology
topic Human papillomavirus
Cervical cancer
Self-sampling
Molecular test
Screening
Science & Technology
description Cervical cancer is the second most common cancer among Brazilian women. High-risk human papillomavirus (hr-HPV) persistence is the primary cause of cervical neoplasia. Early detection of hr-HPV is important for identifying women at risk for developing cervical lesions. Approximately 85% of new cases of cervical cancer worldwide and 50% of the total cervical cancer deaths occurred in developing countries. Here, a new methodology to support a cervical cancer screening program was evaluated in women from various Brazilian regions. METHODS: Two thousand women aged 18-77years were enrolled in an opportunistic cervical cancer screening program and were randomized into self-vaginal or health professional-guided cervical sampling groups. The Qiagen careHPV™ test was performed on all samples. Pap tests were performed on all women using liquid-based cytology. RESULTS: Positive hr-HPV results were obtained in 12.3% (245/2000) of women; similar rates were observed in self- or health professional-collected samples. Eighty-nine percent (1719/2000) of cervical cytologies classified as normal were negative to hr-HPV. Among the cytological samples, 36.6% classified as ASC-US+ were positive to hr-HPV, 78.8% were LSIL and 75.0% were HSIL. CONCLUSIONS: Self-sampled and health professional-sampled vaginal/cervical specimens did not differ in their rates of detection of hr-HPV. Therefore, HPV DNA testing in self-sampled vaginal cells is an alternative to primary screening in low-resource settings.
publishDate 2013
dc.date.none.fl_str_mv 2013
2013-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/1822/25221
url http://hdl.handle.net/1822/25221
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0090-8258
10.1016/j.ygyno.2013.07.092
23880151
www.journals.elsevier.com/gynecologic-oncology/?
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dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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