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Article: The impact of quadrivalent human papillomavirus (HPV; Types 6, 11, 16, and 18) L1 virus-like particle vaccine on infection and disease due to oncogenic nonvaccine HPV types in generally HPV-naive women aged 16-26 years
Title | The impact of quadrivalent human papillomavirus (HPV; Types 6, 11, 16, and 18) L1 virus-like particle vaccine on infection and disease due to oncogenic nonvaccine HPV types in generally HPV-naive women aged 16-26 years |
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Authors | Brown, DRKjaer, SKSigurdsson, KIversen, OEMauricio, HAWheeler, CMPerez, GKoutsky, LATay, EHGarcia, PAult, KAGarland, SMLeodolter, SOlsson, SETang, GWKFerris, DGPaavonen, JSteben, MBosch, FXDillner, JJoura, EAKurman, RJMajewski, SMuñoz, NMyers, ERVilla, LLTaddeo, FJRoberts, CTadesse, ABryan, JLupinacci, LCGiacoletti, KEDSings, HLJames, MHesley, TMBarra, E |
Issue Date | 2009 |
Publisher | Oxford University Press. The Journal's web site is located at http://jid.oxfordjournals.org |
Citation | Journal Of Infectious Diseases, 2009, v. 199 n. 7, p. 926-935 How to Cite? |
Abstract | Background. Human papillomavirus (HPV)-6/11/16/18 vaccine reduces the risk of HPV-6/11/16/18-related cervical intraepithelial neoplasia (CIN) 1-3 or adenocarcinoma in situ (AIS). Here, its impact on CIN1-3/AIS associated with nonvaccine oncogenic HPV types was evaluated. Methods. We enrolled 17,622 women aged 16-26 years. All underwent cervicovaginal sampling and Pap testing at regular intervals for up to 4 years. HPV genotying was performed for biopsy samples, and histological diagnoses were determined by a pathology panel. Analyses were conducted among subjects who were negative for 14 HPV types on day 1. Prespecified analyses included infection of-6 months' duration and CIN1-3/AIS due to the 2 and 5 most common HPV types in cervical cancer after HPV types 16 and 18, as well as all tested nonvaccine types. Results. Vaccination reduced the incidence of HPV-31/45 infection by 40.3% (95% confidence interval [CI], 13.9% to 59.0%) and of CIN1-3/AIS by 43.6% (95% CI, 12.9% to 64.1%), respectively. The reduction in HPV-31/ 33/45/52/58 infection and CIN1-3/AIS was 25.0% (95% CI, 5.0% to 40.9%) and 29.2% (95% CI, 8.3% to 45.5%), respectively. Efficacy for CIN2-3/AIS associated with the 10 nonvaccine HPV types was 32.5% (95% CI, 6.0% to 51.9%). Reductions were most notable for HPV-31. Conclusions. HPV-6/11/16/18 vaccine reduced the risk of CIN2-3/AIS associated with nonvaccine types responsible for 20% of cervical cancers. The clinical benefit of cross-protection is not expected to be fully additive to the efficacy already observed against HPV-6/11/16/18-related disease, because women may have >1 CIN lesion, each associated with a different HPV type. Trial registration. ClinicalTrials.gov identifiers: NCT00092521, NCT00092534, and NCT00092482. © 2009 by the Infectious Diseases Society of America. |
Persistent Identifier | http://hdl.handle.net/10722/60344 |
ISSN | 2023 Impact Factor: 5.0 2023 SCImago Journal Rankings: 2.387 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Brown, DR | en_HK |
dc.contributor.author | Kjaer, SK | en_HK |
dc.contributor.author | Sigurdsson, K | en_HK |
dc.contributor.author | Iversen, OE | en_HK |
dc.contributor.author | Mauricio, HA | en_HK |
dc.contributor.author | Wheeler, CM | en_HK |
dc.contributor.author | Perez, G | en_HK |
dc.contributor.author | Koutsky, LA | en_HK |
dc.contributor.author | Tay, EH | en_HK |
dc.contributor.author | Garcia, P | en_HK |
dc.contributor.author | Ault, KA | en_HK |
dc.contributor.author | Garland, SM | en_HK |
dc.contributor.author | Leodolter, S | en_HK |
dc.contributor.author | Olsson, SE | en_HK |
dc.contributor.author | Tang, GWK | en_HK |
dc.contributor.author | Ferris, DG | en_HK |
dc.contributor.author | Paavonen, J | en_HK |
dc.contributor.author | Steben, M | en_HK |
dc.contributor.author | Bosch, FX | en_HK |
dc.contributor.author | Dillner, J | en_HK |
dc.contributor.author | Joura, EA | en_HK |
dc.contributor.author | Kurman, RJ | en_HK |
dc.contributor.author | Majewski, S | en_HK |
dc.contributor.author | Muñoz, N | en_HK |
dc.contributor.author | Myers, ER | en_HK |
dc.contributor.author | Villa, LL | en_HK |
dc.contributor.author | Taddeo, FJ | en_HK |
dc.contributor.author | Roberts, C | en_HK |
dc.contributor.author | Tadesse, A | en_HK |
dc.contributor.author | Bryan, J | en_HK |
dc.contributor.author | Lupinacci, LC | en_HK |
dc.contributor.author | Giacoletti, KED | en_HK |
dc.contributor.author | Sings, HL | en_HK |
dc.contributor.author | James, M | en_HK |
dc.contributor.author | Hesley, TM | en_HK |
dc.contributor.author | Barra, E | en_HK |
dc.date.accessioned | 2010-05-31T04:08:46Z | - |
dc.date.available | 2010-05-31T04:08:46Z | - |
dc.date.issued | 2009 | en_HK |
dc.identifier.citation | Journal Of Infectious Diseases, 2009, v. 199 n. 7, p. 926-935 | en_HK |
dc.identifier.issn | 0022-1899 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/60344 | - |
dc.description.abstract | Background. Human papillomavirus (HPV)-6/11/16/18 vaccine reduces the risk of HPV-6/11/16/18-related cervical intraepithelial neoplasia (CIN) 1-3 or adenocarcinoma in situ (AIS). Here, its impact on CIN1-3/AIS associated with nonvaccine oncogenic HPV types was evaluated. Methods. We enrolled 17,622 women aged 16-26 years. All underwent cervicovaginal sampling and Pap testing at regular intervals for up to 4 years. HPV genotying was performed for biopsy samples, and histological diagnoses were determined by a pathology panel. Analyses were conducted among subjects who were negative for 14 HPV types on day 1. Prespecified analyses included infection of-6 months' duration and CIN1-3/AIS due to the 2 and 5 most common HPV types in cervical cancer after HPV types 16 and 18, as well as all tested nonvaccine types. Results. Vaccination reduced the incidence of HPV-31/45 infection by 40.3% (95% confidence interval [CI], 13.9% to 59.0%) and of CIN1-3/AIS by 43.6% (95% CI, 12.9% to 64.1%), respectively. The reduction in HPV-31/ 33/45/52/58 infection and CIN1-3/AIS was 25.0% (95% CI, 5.0% to 40.9%) and 29.2% (95% CI, 8.3% to 45.5%), respectively. Efficacy for CIN2-3/AIS associated with the 10 nonvaccine HPV types was 32.5% (95% CI, 6.0% to 51.9%). Reductions were most notable for HPV-31. Conclusions. HPV-6/11/16/18 vaccine reduced the risk of CIN2-3/AIS associated with nonvaccine types responsible for 20% of cervical cancers. The clinical benefit of cross-protection is not expected to be fully additive to the efficacy already observed against HPV-6/11/16/18-related disease, because women may have >1 CIN lesion, each associated with a different HPV type. Trial registration. ClinicalTrials.gov identifiers: NCT00092521, NCT00092534, and NCT00092482. © 2009 by the Infectious Diseases Society of America. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Oxford University Press. The Journal's web site is located at http://jid.oxfordjournals.org | en_HK |
dc.relation.ispartof | Journal of Infectious Diseases | en_HK |
dc.title | The impact of quadrivalent human papillomavirus (HPV; Types 6, 11, 16, and 18) L1 virus-like particle vaccine on infection and disease due to oncogenic nonvaccine HPV types in generally HPV-naive women aged 16-26 years | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Tang, GWK:gwktang@hkucc.hku.hk | en_HK |
dc.identifier.authority | Tang, GWK=rp00328 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1086/597307 | en_HK |
dc.identifier.scopus | eid_2-s2.0-65549109389 | en_HK |
dc.identifier.hkuros | 155035 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-65549109389&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 199 | en_HK |
dc.identifier.issue | 7 | en_HK |
dc.identifier.spage | 926 | en_HK |
dc.identifier.epage | 935 | en_HK |
dc.identifier.isi | WOS:000264056600003 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Brown, DR=7407095050 | en_HK |
dc.identifier.scopusauthorid | Kjaer, SK=7004418213 | en_HK |
dc.identifier.scopusauthorid | Sigurdsson, K=35475355400 | en_HK |
dc.identifier.scopusauthorid | Iversen, OE=7102966661 | en_HK |
dc.identifier.scopusauthorid | Mauricio, HA=36710324400 | en_HK |
dc.identifier.scopusauthorid | Wheeler, CM=7202505711 | en_HK |
dc.identifier.scopusauthorid | Perez, G=16307983600 | en_HK |
dc.identifier.scopusauthorid | Koutsky, LA=7006120337 | en_HK |
dc.identifier.scopusauthorid | Tay, EH=7004902850 | en_HK |
dc.identifier.scopusauthorid | Garcia, P=7201693727 | en_HK |
dc.identifier.scopusauthorid | Ault, KA=7005241226 | en_HK |
dc.identifier.scopusauthorid | Garland, SM=7102220459 | en_HK |
dc.identifier.scopusauthorid | Leodolter, S=7005056838 | en_HK |
dc.identifier.scopusauthorid | Olsson, SE=7202623557 | en_HK |
dc.identifier.scopusauthorid | Tang, GWK=7401633864 | en_HK |
dc.identifier.scopusauthorid | Ferris, DG=17634377600 | en_HK |
dc.identifier.scopusauthorid | Paavonen, J=7102724434 | en_HK |
dc.identifier.scopusauthorid | Steben, M=6602790643 | en_HK |
dc.identifier.scopusauthorid | Bosch, FX=7201833375 | en_HK |
dc.identifier.scopusauthorid | Dillner, J=7007135194 | en_HK |
dc.identifier.scopusauthorid | Joura, EA=7004817276 | en_HK |
dc.identifier.scopusauthorid | Kurman, RJ=7101640655 | en_HK |
dc.identifier.scopusauthorid | Majewski, S=7103224726 | en_HK |
dc.identifier.scopusauthorid | Muñoz, N=7102360543 | en_HK |
dc.identifier.scopusauthorid | Myers, ER=35433205900 | en_HK |
dc.identifier.scopusauthorid | Villa, LL=7102824355 | en_HK |
dc.identifier.scopusauthorid | Taddeo, FJ=6603004214 | en_HK |
dc.identifier.scopusauthorid | Roberts, C=35474924800 | en_HK |
dc.identifier.scopusauthorid | Tadesse, A=6602812727 | en_HK |
dc.identifier.scopusauthorid | Bryan, J=7202481712 | en_HK |
dc.identifier.scopusauthorid | Lupinacci, LC=16307166200 | en_HK |
dc.identifier.scopusauthorid | Giacoletti, KED=15131768700 | en_HK |
dc.identifier.scopusauthorid | Sings, HL=8401383500 | en_HK |
dc.identifier.scopusauthorid | James, M=10438802400 | en_HK |
dc.identifier.scopusauthorid | Hesley, TM=6603486789 | en_HK |
dc.identifier.scopusauthorid | Barra, E=36709232100 | en_HK |
dc.identifier.citeulike | 4089363 | - |
dc.identifier.issnl | 0022-1899 | - |