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...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2007
- Institución:
- Universidad del Rosario
- Repositorio:
- 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
- Rights
- License
- Abierto (Texto Completo)
id |
EDOCUR2_729a6790e3e129a43f0a9ef730b494a6 |
---|---|
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 |
_version_ |
1814167559682916352 |