Quadrivalent vaccine against human papillomavirus to prevent high-grade cervical lesions

BACKGROUND Human papillomavirus types 16 (HPV-16) and 18 (HPV-18) cause approximately 70% of cervical cancers worldwide. A phase 3 trial was conducted to evaluate a quadrivalent vaccine against HPV types 6, 11, 16, and 18 (HPV-6/11/16/18) for the prevention of high-grade cervical lesions associated...

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Fecha de publicación:
2007
Institución:
Universidad del Rosario
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Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/26826
Acceso en línea:
https://doi.org/10.1056/NEJMoa061741
https://repository.urosario.edu.co/handle/10336/26826
Palabra clave:
Hematology
Oncology gynecologic
Oncology dermatology
Vaccines genetics
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oai_identifier_str oai:repository.urosario.edu.co:10336/26826
network_acronym_str EDOCUR2
network_name_str Repositorio EdocUR - U. Rosario
repository_id_str
spelling 396948886002020-08-19T14:40:19Z2020-08-19T14:40:19Z2007-05-10BACKGROUND Human papillomavirus types 16 (HPV-16) and 18 (HPV-18) cause approximately 70% of cervical cancers worldwide. A phase 3 trial was conducted to evaluate a quadrivalent vaccine against HPV types 6, 11, 16, and 18 (HPV-6/11/16/18) for the prevention of high-grade cervical lesions associated with HPV-16 and HPV-18. METHODS In this randomized, double-blind trial, we assigned 12,167 women between the ages of 15 and 26 years to receive three doses of either HPV-6/11/16/18 vaccine or placebo, administered at day 1, month 2, and month 6. The primary analysis was performed for a per-protocol susceptible population that included 5305 women in the vaccine group and 5260 in the placebo group who had no virologic evidence of infection with HPV-16 or HPV-18 through 1 month after the third dose (month 7). The primary composite end point was cervical intraepithelial neoplasia grade 2 or 3, adenocarcinoma in situ, or cervical cancer related to HPV-16 or HPV-18. RESULTS Subjects were followed for an average of 3 years after receiving the first dose of vaccine or placebo. Vaccine efficacy for the prevention of the primary composite end point was 98% (95.89% confidence interval [CI], 86 to 100) in the per-protocol susceptible population and 44% (95% CI, 26 to 58) in an intention-to-treat population of all women who had undergone randomization (those with or without previous infection). The estimated vaccine efficacy against all high-grade cervical lesions, regardless of causal HPV type, in this intention-to-treat population was 17% (95% CI, 1 to 31). CONCLUSIONS In young women who had not been previously infected with HPV-16 or HPV-18, those in the vaccine group had a significantly lower occurrence of high-grade cervical intraepithelial neoplasia related to HPV-16 or HPV-18 than did those in the placebo group. (ClinicalTrials.gov number, NCT00092534. opens in new tab.)application/pdfhttps://doi.org/10.1056/NEJMoa061741ISSN: 0028-4793EISSN: 1533-4406https://repository.urosario.edu.co/handle/10336/26826engMassachusetts Medical Society1927No. 191915The New England Journal of MedicineVol. 356The New England Journal of Medicine, ISSN: 0028-4793;EISSN: 1533-4406, Vol.356, No.19 (2007); pp. 1915-1927https://www.nejm.org/doi/pdf/10.1056/NEJMoa061741?articleTools=trueAbierto (Texto Completo)http://purl.org/coar/access_right/c_abf2The New England Journal of Medicineinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURHematologyOncology gynecologicOncology dermatologyVaccines geneticsQuadrivalent vaccine against human papillomavirus to prevent high-grade cervical lesionsVacuna cuadrivalente contra el virus del papiloma humano para prevenir lesiones cervicales de alto gradoarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Ruíz Sternberg, Ángela María10336/26826oai:repository.urosario.edu.co:10336/268262020-08-19 09:40:19.806https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv Quadrivalent vaccine against human papillomavirus to prevent high-grade cervical lesions
dc.title.TranslatedTitle.spa.fl_str_mv Vacuna cuadrivalente contra el virus del papiloma humano para prevenir lesiones cervicales de alto grado
title Quadrivalent vaccine against human papillomavirus to prevent high-grade cervical lesions
spellingShingle Quadrivalent vaccine against human papillomavirus to prevent high-grade cervical lesions
Hematology
Oncology gynecologic
Oncology dermatology
Vaccines genetics
title_short Quadrivalent vaccine against human papillomavirus to prevent high-grade cervical lesions
title_full Quadrivalent vaccine against human papillomavirus to prevent high-grade cervical lesions
title_fullStr Quadrivalent vaccine against human papillomavirus to prevent high-grade cervical lesions
title_full_unstemmed Quadrivalent vaccine against human papillomavirus to prevent high-grade cervical lesions
title_sort Quadrivalent vaccine against human papillomavirus to prevent high-grade cervical lesions
dc.subject.keyword.spa.fl_str_mv Hematology
Oncology gynecologic
Oncology dermatology
Vaccines genetics
topic Hematology
Oncology gynecologic
Oncology dermatology
Vaccines genetics
description BACKGROUND Human papillomavirus types 16 (HPV-16) and 18 (HPV-18) cause approximately 70% of cervical cancers worldwide. A phase 3 trial was conducted to evaluate a quadrivalent vaccine against HPV types 6, 11, 16, and 18 (HPV-6/11/16/18) for the prevention of high-grade cervical lesions associated with HPV-16 and HPV-18. METHODS In this randomized, double-blind trial, we assigned 12,167 women between the ages of 15 and 26 years to receive three doses of either HPV-6/11/16/18 vaccine or placebo, administered at day 1, month 2, and month 6. The primary analysis was performed for a per-protocol susceptible population that included 5305 women in the vaccine group and 5260 in the placebo group who had no virologic evidence of infection with HPV-16 or HPV-18 through 1 month after the third dose (month 7). The primary composite end point was cervical intraepithelial neoplasia grade 2 or 3, adenocarcinoma in situ, or cervical cancer related to HPV-16 or HPV-18. RESULTS Subjects were followed for an average of 3 years after receiving the first dose of vaccine or placebo. Vaccine efficacy for the prevention of the primary composite end point was 98% (95.89% confidence interval [CI], 86 to 100) in the per-protocol susceptible population and 44% (95% CI, 26 to 58) in an intention-to-treat population of all women who had undergone randomization (those with or without previous infection). The estimated vaccine efficacy against all high-grade cervical lesions, regardless of causal HPV type, in this intention-to-treat population was 17% (95% CI, 1 to 31). CONCLUSIONS In young women who had not been previously infected with HPV-16 or HPV-18, those in the vaccine group had a significantly lower occurrence of high-grade cervical intraepithelial neoplasia related to HPV-16 or HPV-18 than did those in the placebo group. (ClinicalTrials.gov number, NCT00092534. opens in new tab.)
publishDate 2007
dc.date.created.spa.fl_str_mv 2007-05-10
dc.date.accessioned.none.fl_str_mv 2020-08-19T14:40:19Z
dc.date.available.none.fl_str_mv 2020-08-19T14:40:19Z
dc.type.eng.fl_str_mv article
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_6501
dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1056/NEJMoa061741
dc.identifier.issn.none.fl_str_mv ISSN: 0028-4793
EISSN: 1533-4406
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/26826
url https://doi.org/10.1056/NEJMoa061741
https://repository.urosario.edu.co/handle/10336/26826
identifier_str_mv ISSN: 0028-4793
EISSN: 1533-4406
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationEndPage.none.fl_str_mv 1927
dc.relation.citationIssue.none.fl_str_mv No. 19
dc.relation.citationStartPage.none.fl_str_mv 1915
dc.relation.citationTitle.none.fl_str_mv The New England Journal of Medicine
dc.relation.citationVolume.none.fl_str_mv Vol. 356
dc.relation.ispartof.spa.fl_str_mv The New England Journal of Medicine, ISSN: 0028-4793;EISSN: 1533-4406, Vol.356, No.19 (2007); pp. 1915-1927
dc.relation.uri.spa.fl_str_mv https://www.nejm.org/doi/pdf/10.1056/NEJMoa061741?articleTools=true
dc.rights.coar.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.rights.acceso.spa.fl_str_mv Abierto (Texto Completo)
rights_invalid_str_mv Abierto (Texto Completo)
http://purl.org/coar/access_right/c_abf2
dc.format.mimetype.none.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv Massachusetts Medical Society
dc.source.spa.fl_str_mv The New England Journal of Medicine
institution Universidad del Rosario
dc.source.instname.none.fl_str_mv instname:Universidad del Rosario
dc.source.reponame.none.fl_str_mv reponame:Repositorio Institucional EdocUR
repository.name.fl_str_mv Repositorio institucional EdocUR
repository.mail.fl_str_mv edocur@urosario.edu.co
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