Sustained efficacy up to 4-5 years of a bivalent L1 virus-like particle vaccine against human papillomavirus types 16 and 18: follow-up from a randomised control trial

被引:1166
作者
Harper, DM
Franco, EL
Wheeler, CM
Moscicki, AB
Romonowski, B
Roteli-Martins, CM
Jenkins, D
Schuind, A
Clemens, SAC
Dubin, G
机构
[1] Dartmouth Med Sch, Norris Cotton Canc Ctr, Dept Obstet & Gynecol, Lebanon, NH 03756 USA
[2] Dartmouth Med Sch, Norris Cotton Canc Ctr, Dept Community & Family Med, Lebanon, NH 03756 USA
[3] McGill Univ, Dept Oncol, Montreal, PQ, Canada
[4] McGill Univ, Dept Epidemiol & Biostat, Montreal, PQ, Canada
[5] Univ New Mexico, Hlth Sci Ctr, Dept Mol Genet & Microbiol, Albuquerque, NM 87131 USA
[6] Univ New Mexico, Hlth Sci Ctr, Dept Obstet & Gynecol, Albuquerque, NM 87131 USA
[7] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
[8] Univ Alberta, Edmonton, AB, Canada
[9] Nove Julho Hosp, Sao Paulo, Brazil
[10] GlaxoSmithKline Biol, Rixensart, Belgium
[11] GlaxoSmithKline Biol, King Of Prussia, PA USA
[12] GlaxoSmithKline Biol, Rio De Janeiro, Brazil
关键词
D O I
10.1016/S0140-6736(06)68439-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Effective vaccination against HPV 16 and HPV 18 to prevent cervical cancer will require a high level of sustained protection against infection and precancerous lesions. Our aim was to assess the long-term efficacy, immunogenicity, and safety of a bivalent HPV-16/18 L1 virus-like particle AS04 vaccine against incident and persistent infection with HPV 16 and HPV 18 and their associated cytological and histological outcomes. Methods We did a follow-up study of our multicentre, double-blind, randomised, placebo-controlled trial reported in 2004. We included women who originally received all three doses of bivalent HPV-16/18 virus-like particle AS04 vaccine (0.5 mL; n=393) or placebo (n=383). We assessed HPV DNA, using cervical samples, and did yearly cervical cytology assessments. We also studied the long-term immunogenicity and safety of the vaccine. Findings More than 98% seropositivity was maintained for HPV-16/18 antibodies during the extended follow-up phase. We noted significant vaccine efficacy against HPV-16 and HPV-18 endpoints: incident infection, 96.9% (95% CI 81.3-99.9); persistent infection: 6 month definition, 94.3 (63.2-99.9); 12 month definition, 100% (33.6-100). In a combined analysis of the initial efficacy and extended follow-up studies, vaccine efficacy of 100% (42.4-100) against cervical intraepithelial neoplasia (CIN) lesions associated with vaccine types. We noted broad protection against cytohistological outcomes beyond that anticipated for HPV 16/18 and protection against incident infection with HPV 45 and HPV 31. The vaccine has a good long-term safety profile. Interpretation Up to 4.5 years, the HPV-16/18 L1 virus-like particle AS04 vaccine is highly immunogenic and safe, and induces a high degree of protection against HPV-16/18 infection and associated cervical lesions. There is also evidence of cross protection.
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页码:1247 / 1255
页数:9
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