Risk of new onset autoimmune disease in 9-to 25-year-old women exposed to human papillomavirus-16/18 AS04-adjuvanted vaccine in the United Kingdom

被引:34
|
作者
Willame, Corinne [1 ]
Rosillon, Dominique [2 ]
Zima, Julia [2 ]
Angelo, Maria-Genalin [2 ]
Stuurman, Anke L. [3 ]
Vroling, Hilde [3 ]
Boggon, Rachael [4 ]
Bunge, Eveline M. [3 ]
Pladevall-Vila, Manel [5 ,6 ]
Baril, Laurence [2 ]
机构
[1] GSK Vaccines, Business & Decis Life Sci, Ave Fleming 20, B-1300 Wavre, Belgium
[2] GSK Vaccines, Wavre, Belgium
[3] Pallas Hlth Res & Consultancy, Rotterdam, Netherlands
[4] CPRD Res Grp, London, England
[5] RTI Hlth Solut, Barcelona, Spain
[6] Henry Ford Hlth Syst, Ctr Hlth Policy & Hlth Serv Res, Detroit, MI USA
关键词
autoimmune conditions; human papilloma virus; human papillomavirus vaccine; post-licensure safety study; vaccination; vaccine safety; POST-LICENSURE SAFETY; BLIND PATRICIA TRIAL; OF-STUDY ANALYSIS; ADOLESCENT GIRLS; CLINICAL-TRIALS; CERVICAL-CANCER; POOLED ANALYSIS; FOLLOW-UP; EFFICACY; SURVEILLANCE;
D O I
10.1080/21645515.2016.1199308
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To assess the risk of autoimmune disease (AD) in 9-25 year-old women within 1 year after the first AS04-HPV-16/18vaccine dose, a retrospective, observational database cohort study was conducted using CPRD GOLD. From CPRD GOLD 4 cohorts (65,000 subjects each) were retrieved: 1 exposed female cohort (received >= 1 AS04-HPV-16/18 vaccine dose between Sep2008-Aug2010) and 3 unexposed cohorts: historical female (Sep2005-Aug2007), concurrent male, and historical male. Co-primary endpoints were confirmed neuroinflammatory/ophthalmic AD and other AD, secondary endpoints were confirmed individual AD. Risk of new onset of AD was compared between cohorts (reference: historical cohort) using Poisson regression. The main analysis using confirmed cases showed no neuroinflammatory/ophthalmic AD cases in the female exposed cohort. Incidence rate ratio (IRR) (95% CI) of other AD was 1.41 (0.86 to 2.31) in female and 1.77 (0.94 to 3.35) in male cohorts when compared to the female and male historical cohort, respectively. Secondary endpoints were evaluated for diseases with >10 cases, which were Crohn's disease (IRR: 1.21 [0.37 to 3.95] for female and 4.22 [0.47 to 38.02] for male cohorts), autoimmune thyroiditis (IRR: 3.75 [1.25 to 11.31] for female and no confirmed cases for male cohorts) and type 1 diabetes (IRR: 0.30 [0.11 to 0.83] for female and 2.46 [1.08 to 5.60] for male cohorts). Analysis using confirmed and non-confirmed cases showed similar results, except for autoimmune thyroiditis in females, IRR: 1.45 (0.79 to 2.64). There was no evidence of an increased risk of AD in women aged 9 to 25 years after AS04-HPV-16/18 vaccination.
引用
收藏
页码:2862 / 2871
页数:10
相关论文
共 41 条
  • [31] Efficacy of Human Papillomavirus 16 and 18 (HPV-16/18) AS04-Adjuvanted Vaccine against Cervical Infection and Precancer in Young Women: Final Event-Driven Analysis of the Randomized, Double-Blind PATRICIA Trial
    Apter, Dan
    Wheeler, Cosette M.
    Paavonen, Jorma
    Castellsague, Xavier
    Garland, Suzanne M.
    Skinner, S. Rachel
    Naud, Paulo
    Salmeron, Jorge
    Chow, Song-Nan
    Kitchener, Henry C.
    Teixeira, Julio C.
    Jaisamram, Unnop
    Limson, Genara
    Szarewski, Anne
    Romanowski, Barbara
    Aoki, Fred Y.
    Schwarz, Tino F.
    Poppe, Willy A. J.
    Xavier Bosch, F.
    Mindel, Adrian
    De Sutter, Philippe
    Hardt, Karin
    Zahaf, Toufik
    Descamps, Dominique
    Struyf, Frank
    Lehtinen, Matti
    Dubin, Gary
    CLINICAL AND VACCINE IMMUNOLOGY, 2015, 22 (04) : 361 - 373
  • [32] Lessons Learned from Implementation of a Prospective, Observational Cohort Study to Assess Risk of Spontaneous Abortion (SA) Following Administration of Human Papillomavirus (HPV)-16/18 AS04-Adjuvanted Vaccine around Conception
    Chambers, Christina
    Johnson, Diana
    Xu, Ronghui
    Rosillon, Dominique
    den Bosch, Judithvan
    Baril, Laurence
    Taylor, Sylvia
    PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2013, 22 : 140 - 141
  • [33] Six-year multi-centre, observational, post-marketing surveillance of the safety of the HPV-16/18 AS04-adjuvanted vaccine in women aged 10-25years in Korea
    Kim, Chul-Jung
    Song, Rok
    Chen, Jing
    Da Silva, Fernanda Tavares
    Gopala, Kusuma B.
    Kim, Joon Hyung
    Bi, Dan
    Park, Jong Sup
    PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2017, 26 (07) : 837 - 842
  • [34] Design and Feasibility of a Study Using the Clinical Practice Research Datalink General Practice OnLine Database (CPRD GOLD) To Assess the Risk of New Onset of Auto-Immune Diseases (NOAD) Following Administration of the Human Papillomavirus (HPV)-16/18 AS04-Adjuvanted Vaccine
    Rosillon, Dominique
    Willame, Corinne
    Pladevall, Manel
    Zima, Julia
    van den Bosch, Judith H.
    Bunge, Eveline
    van Staa, Tjeerd
    Boggon, Rachael
    Baril, Laurence
    PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2014, 23 : 164 - 165
  • [35] Efficacy of human papillomavirus (HPV)-16/18 AS04-adjuvanted vaccine against cervical infection and precancer caused by oncogenic HPV types (PATRICIA): final analysis of a double-blind, randomised study in young women
    Paovonen, J.
    Naud, P.
    Salmeron, J.
    Wheeler, C. M.
    Chow, S-N
    Apter, D.
    Kitchener, H.
    Castellsague, X.
    Teixeira, J. C.
    Skinner, S. R.
    Hedrick, J.
    Jaisamrarn, U.
    Limson, G.
    Garland, S.
    Szarewski, A.
    Romanowski, B.
    Aoki, F. Y.
    Schwarz, T. F.
    Poppe, W. A. J.
    Bosch, F. X.
    Jenkins, D.
    Hardt, K.
    Zahaf, T.
    Descamps, D.
    Struyf, F.
    Lehtinen, M.
    Dubin, G.
    LANCET, 2009, 374 (9686): : 301 - 314
  • [36] Comparison of long-term immunogenicity and safety of human papillomavirus (HPV)-16/18 AS04-adjuvanted vaccine and HPV-6/11/16/18 vaccine in healthy women aged 18-45 years: End-of-study analysis of a Phase III randomized trial
    Einstein, Mark H.
    Takacs, Peter
    Chatterjee, Archana
    Sperling, Rhoda S.
    Chakhtoura, Nahida
    Blatter, Mark M.
    Lalezari, Jacob
    David, Marie-Pierre
    Lin, Lan
    Struyf, Frank
    Dubin, Gary
    HUMAN VACCINES & IMMUNOTHERAPEUTICS, 2014, 10 (12) : 3435 - 3445
  • [37] Comparative humoral and cellular immunogenicity and safety of human papillomavirus (HPV)-16/18 AS04-adjuvanted vaccine and HPV-6/11/16/18 vaccine in healthy women aged 18-45 years: Follow-up through Month 48 in a Phase III randomized study
    Einstein, Mark H.
    Levin, Myron J.
    Chatterjee, Archana
    Chakhtoura, Nahida
    Takacs, Peter
    Catteau, Gregory
    Dessy, Francis J.
    Moris, Philippe
    Lin, Lan
    Struyf, Frank
    Dubin, Gary
    HUMAN VACCINES & IMMUNOTHERAPEUTICS, 2014, 10 (12) : 3455 - 3465
  • [38] Design and Feasibility of a Study Using the Clinical Practice Research Datalink General Practice OnLine Database (CPRD GOLD) to Assess the Risk of Spontaneous Abortion (SA) Following Administration of the Human Papillomavirus (HPV)-16/18 AS04-Adjuvanted Vaccine
    Rosillon, Dominique
    Willame, Corinne
    Logie, John
    Taylor, Sylvia
    Bauchau, Vincent
    Angelo, Maria-Genalin
    Zima, Julia
    den Bosch, Judithvan
    Staa, Tjeerdvan
    Boggon, Rachael
    Chambers, Christina
    Hernandez-Diaz, Sonia
    Baril, Laurence
    PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2013, 22 : 140 - 140
  • [39] Comparative immunogenicity and safety of human papillomavirus (HPV)-16/18 AS04-adjuvanted vaccine and HPV-6/11/16/18 vaccine administered according to 2-and 3-dose schedules in girls aged 9-14 years: Results to month 12 from a randomized trial
    Leung, Ting Fan
    Liu, Anthony Pak-Yin
    Lim, Fong Seng
    Thollot, Franck
    Oh, Helen May Lin
    Lee, Bee Wah
    Rombo, Lars
    Tan, Ngiap Chuan
    Rouzier, Roman
    Friel, Damien
    De Muynck, Benoit
    De Simoni, Stephanie
    Suryakiran, Pemmaraju
    Hezareh, Marjan
    Folschweiller, Nicolas
    Thomas, Florence
    Struyf, Frank
    HUMAN VACCINES & IMMUNOTHERAPEUTICS, 2015, 11 (07) : 1689 - 1702
  • [40] Efficacy of the human papillomavirus (HPV)-16/18 AS04-adjuvanted vaccine against cervical intraepithelial neoplasia and cervical infection in young Japanese women Open follow-up of a randomized clinical trial up to 4 years post-vaccination
    Konno, Ryo
    Yoshikawa, Hiroyuki
    Okutani, Marie
    Quint, Wim
    Suryakiran, Pemmaraju V.
    Lin, Lan
    Struyf, Frank
    HUMAN VACCINES & IMMUNOTHERAPEUTICS, 2014, 10 (07) : 1781 - 1794