Effect of the human papillomavirus (HPV) quadrivalent vaccine in a subgroup of women with cervical and vulvar disease: Retrospective pooled analysis of trial data

Elmar A. Joura, Suzanne M. Garland, Jorma Paavonen, Daron Gale Ferris, Gonzalo Perez, Kevin A. Ault, Warner K. Huh, Heather L. Sings, Margaret K. James, Richard M. Haupt

Research output: Contribution to journalArticle

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Abstract

Objectives: To determine the effect of human papillomavirus (HPV) quadrivalent vaccine on the risk of developing subsequent disease after an excisional procedure for cervical intraepithelial neoplasia or diagnosis of genital warts, vulvar intraepithelial neoplasia, or vaginal intraepithelial neoplasia. Design: Retrospective analysis of data from two international, double blind, placebo controlled, randomised efficacy trials of quadrivalent HPV vaccine (protocol 013 (FUTURE I) and protocol 015 (FUTURE II)). Setting: Primary care centres and university or hospital associated health centres in 24 countries and territories around the world. Participants: Among 17 622 women aged 15-26 years who underwent 1:1 randomisation to vaccine or placebo, 2054 received cervical surgery or were diagnosed with genital warts, vulvar intraepithelial neoplasia, or vaginal intraepithelial neoplasia. Intervention: Three doses of quadrivalent HPV vaccine or placebo at day 1, month 2, and month 6. Main outcome measures: Incidence of HPV related disease from 60 days after treatment or diagnosis, expressed as the number of women with an end point per 100 person years at risk. Results: A total of 587 vaccine and 763 placebo recipients underwent cervical surgery. The incidence of any subsequent HPV related disease was 6.6 and 12.2 in vaccine and placebo recipients respectively (46.2% reduction (95% confidence interval 22.5% to 63.2%) with vaccination). Vaccination was associated with a significant reduction in risk of any subsequent high grade disease of the cervix by 64.9% (20.1% to 86.3%). A total of 229 vaccine recipients and 475 placebo recipients were diagnosed with genital warts, vulvar intraepithelial neoplasia, or vaginal intraepithelial neoplasia, and the incidence of any subsequent HPV related disease was 20.1 and 31.0 in vaccine and placebo recipients respectively (35.2% reduction (13.8% to 51.8%)). Conclusions: Previous vaccination with quadrivalent HPV vaccine among women who had surgical treatment for HPV related disease significantly reduced the incidence of subsequent HPV related disease, including high grade disease. Trial registrations: NCT00092521 and NCT00092534.

Original languageEnglish (US)
Article numbere1401
JournalBMJ (Online)
Volume344
Issue number7851
DOIs
StatePublished - Apr 7 2012

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Vulvar Diseases
Papillomavirus Vaccines
Placebos
Vaccines
Condylomata Acuminata
Neoplasms
Vaccination
Incidence
Uterine Cervical Diseases
Cervical Intraepithelial Neoplasia
Risk Reduction Behavior
Random Allocation
Primary Health Care
Randomized Controlled Trials
Outcome Assessment (Health Care)
Confidence Intervals

ASJC Scopus subject areas

  • Medicine(all)

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Effect of the human papillomavirus (HPV) quadrivalent vaccine in a subgroup of women with cervical and vulvar disease : Retrospective pooled analysis of trial data. / Joura, Elmar A.; Garland, Suzanne M.; Paavonen, Jorma; Ferris, Daron Gale; Perez, Gonzalo; Ault, Kevin A.; Huh, Warner K.; Sings, Heather L.; James, Margaret K.; Haupt, Richard M.

In: BMJ (Online), Vol. 344, No. 7851, e1401, 07.04.2012.

Research output: Contribution to journalArticle

Joura, Elmar A. ; Garland, Suzanne M. ; Paavonen, Jorma ; Ferris, Daron Gale ; Perez, Gonzalo ; Ault, Kevin A. ; Huh, Warner K. ; Sings, Heather L. ; James, Margaret K. ; Haupt, Richard M. / Effect of the human papillomavirus (HPV) quadrivalent vaccine in a subgroup of women with cervical and vulvar disease : Retrospective pooled analysis of trial data. In: BMJ (Online). 2012 ; Vol. 344, No. 7851.
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abstract = "Objectives: To determine the effect of human papillomavirus (HPV) quadrivalent vaccine on the risk of developing subsequent disease after an excisional procedure for cervical intraepithelial neoplasia or diagnosis of genital warts, vulvar intraepithelial neoplasia, or vaginal intraepithelial neoplasia. Design: Retrospective analysis of data from two international, double blind, placebo controlled, randomised efficacy trials of quadrivalent HPV vaccine (protocol 013 (FUTURE I) and protocol 015 (FUTURE II)). Setting: Primary care centres and university or hospital associated health centres in 24 countries and territories around the world. Participants: Among 17 622 women aged 15-26 years who underwent 1:1 randomisation to vaccine or placebo, 2054 received cervical surgery or were diagnosed with genital warts, vulvar intraepithelial neoplasia, or vaginal intraepithelial neoplasia. Intervention: Three doses of quadrivalent HPV vaccine or placebo at day 1, month 2, and month 6. Main outcome measures: Incidence of HPV related disease from 60 days after treatment or diagnosis, expressed as the number of women with an end point per 100 person years at risk. Results: A total of 587 vaccine and 763 placebo recipients underwent cervical surgery. The incidence of any subsequent HPV related disease was 6.6 and 12.2 in vaccine and placebo recipients respectively (46.2{\%} reduction (95{\%} confidence interval 22.5{\%} to 63.2{\%}) with vaccination). Vaccination was associated with a significant reduction in risk of any subsequent high grade disease of the cervix by 64.9{\%} (20.1{\%} to 86.3{\%}). A total of 229 vaccine recipients and 475 placebo recipients were diagnosed with genital warts, vulvar intraepithelial neoplasia, or vaginal intraepithelial neoplasia, and the incidence of any subsequent HPV related disease was 20.1 and 31.0 in vaccine and placebo recipients respectively (35.2{\%} reduction (13.8{\%} to 51.8{\%})). Conclusions: Previous vaccination with quadrivalent HPV vaccine among women who had surgical treatment for HPV related disease significantly reduced the incidence of subsequent HPV related disease, including high grade disease. Trial registrations: NCT00092521 and NCT00092534.",
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