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Impact of partial bivalent HPV vaccination on vaccine-type infection: a population-based analysis

BACKGROUND: Data on the effectiveness of one dose of HPV vaccine are lacking, particularly in population-based settings. Data from a national HPV immunisation catch-up programme of 14–18-year-old girls were used to assess the effectiveness of<3 doses of the bivalent vaccine on vaccine-type and cr...

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Autores principales: Cuschieri, K, Kavanagh, K, Moore, C, Bhatia, R, Love, J, Pollock, K G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4891516/
https://www.ncbi.nlm.nih.gov/pubmed/27115467
http://dx.doi.org/10.1038/bjc.2016.97
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author Cuschieri, K
Kavanagh, K
Moore, C
Bhatia, R
Love, J
Pollock, K G
author_facet Cuschieri, K
Kavanagh, K
Moore, C
Bhatia, R
Love, J
Pollock, K G
author_sort Cuschieri, K
collection PubMed
description BACKGROUND: Data on the effectiveness of one dose of HPV vaccine are lacking, particularly in population-based settings. Data from a national HPV immunisation catch-up programme of 14–18-year-old girls were used to assess the effectiveness of<3 doses of the bivalent vaccine on vaccine-type and cross-reactive-type HPV infection. METHODS: Cervical samples from women attending for their first cervical smear, which had been genotyped for HPV as part of a longitudinal HPV surveillance programme were linked to immunisation records to establish the number of vaccine doses (0, 1, 2 and 3) administered. Vaccine effectiveness (VE) adjusted for deprivation and age at first dose, was assessed for prevalent HPV 16/18 and HPV 31/33/45 infection. RESULTS: VE for prevalent HPV 16/18 infection associated with 1, 2 and 3 doses was 48.2% (95% CI 16.8, 68.9), 54.8% (95% CI 30.7, 70.8) and 72.8% (95% CI 62.8, 80.3). Equivalent VE for prevalent HPV 31/33/45 infection was −1.62% (95% CI −85.1, 45.3), 48.3% (95% CI 7.6, 71.8) and 55.2% (95% CI 32.6, 70.2). CONCLUSIONS: Consistent with recent aggregated trial data, we demonstrate the potential effectiveness of even one dose of HPV vaccine on vaccine-type infection. Given that these women were immunised as part of a catch-up campaign, the VE observed in this study is likely to be an underestimate of what will occur in girls vaccinated at younger ages. Further population-based studies which look at the clinical efficacy of one-dose schedules are warranted.
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spelling pubmed-48915162017-05-24 Impact of partial bivalent HPV vaccination on vaccine-type infection: a population-based analysis Cuschieri, K Kavanagh, K Moore, C Bhatia, R Love, J Pollock, K G Br J Cancer Short Communication BACKGROUND: Data on the effectiveness of one dose of HPV vaccine are lacking, particularly in population-based settings. Data from a national HPV immunisation catch-up programme of 14–18-year-old girls were used to assess the effectiveness of<3 doses of the bivalent vaccine on vaccine-type and cross-reactive-type HPV infection. METHODS: Cervical samples from women attending for their first cervical smear, which had been genotyped for HPV as part of a longitudinal HPV surveillance programme were linked to immunisation records to establish the number of vaccine doses (0, 1, 2 and 3) administered. Vaccine effectiveness (VE) adjusted for deprivation and age at first dose, was assessed for prevalent HPV 16/18 and HPV 31/33/45 infection. RESULTS: VE for prevalent HPV 16/18 infection associated with 1, 2 and 3 doses was 48.2% (95% CI 16.8, 68.9), 54.8% (95% CI 30.7, 70.8) and 72.8% (95% CI 62.8, 80.3). Equivalent VE for prevalent HPV 31/33/45 infection was −1.62% (95% CI −85.1, 45.3), 48.3% (95% CI 7.6, 71.8) and 55.2% (95% CI 32.6, 70.2). CONCLUSIONS: Consistent with recent aggregated trial data, we demonstrate the potential effectiveness of even one dose of HPV vaccine on vaccine-type infection. Given that these women were immunised as part of a catch-up campaign, the VE observed in this study is likely to be an underestimate of what will occur in girls vaccinated at younger ages. Further population-based studies which look at the clinical efficacy of one-dose schedules are warranted. Nature Publishing Group 2016-05-24 2016-04-26 /pmc/articles/PMC4891516/ /pubmed/27115467 http://dx.doi.org/10.1038/bjc.2016.97 Text en Copyright © 2016 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Short Communication
Cuschieri, K
Kavanagh, K
Moore, C
Bhatia, R
Love, J
Pollock, K G
Impact of partial bivalent HPV vaccination on vaccine-type infection: a population-based analysis
title Impact of partial bivalent HPV vaccination on vaccine-type infection: a population-based analysis
title_full Impact of partial bivalent HPV vaccination on vaccine-type infection: a population-based analysis
title_fullStr Impact of partial bivalent HPV vaccination on vaccine-type infection: a population-based analysis
title_full_unstemmed Impact of partial bivalent HPV vaccination on vaccine-type infection: a population-based analysis
title_short Impact of partial bivalent HPV vaccination on vaccine-type infection: a population-based analysis
title_sort impact of partial bivalent hpv vaccination on vaccine-type infection: a population-based analysis
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4891516/
https://www.ncbi.nlm.nih.gov/pubmed/27115467
http://dx.doi.org/10.1038/bjc.2016.97
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