Efficacy, immunogenicity and safety of the HPV‐16/18 AS04‐adjuvanted vaccine in healthy Chinese women aged 18–25 years: Results from a randomized controlled trial

This phase II/III, double‐blind, randomized trial assessed the efficacy, immunogenicity and safety of the human papillomavirus (HPV)‐16/18 AS04‐adjuvanted vaccine in young Chinese women (ClinicalTrials.gov registration NCT00779766). Women aged 18–25 years from Jiangsu province were randomized (1:1)...

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Published inInternational journal of cancer Vol. 135; no. 11; pp. 2612 - 2622
Main Authors Zhu, Feng‐Cai, Chen, Wen, Hu, Yue‐Mei, Hong, Ying, Li, Juan, Zhang, Xun, Zhang, Yi‐Ju, Pan, Qin‐Jing, Zhao, Fang‐Hui, Yu, Jia‐Xi, Zhang, Yan‐Shu, Yang, Xiaoping, Zhang, Cheng‐Fu, Tang, Haiwen, Zhang, Helen, Lebacq, Marie, David, Marie‐Pierre, Datta, Sanjoy K, Struyf, Frank, Bi, Dan, Descamps, Dominique
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.12.2014
BlackWell Publishing Ltd
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Online AccessGet full text
ISSN0020-7136
1097-0215
1097-0215
DOI10.1002/ijc.28897

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Summary:This phase II/III, double‐blind, randomized trial assessed the efficacy, immunogenicity and safety of the human papillomavirus (HPV)‐16/18 AS04‐adjuvanted vaccine in young Chinese women (ClinicalTrials.gov registration NCT00779766). Women aged 18–25 years from Jiangsu province were randomized (1:1) to receive HPV vaccine (n = 3,026) or Al(OH)3 control (n = 3,025) at months 0, 1 and 6. The primary objective was vaccine efficacy (VE) against HPV‐16/18 associated 6‐month persistent infection (PI) and/or cervical intraepithelial neoplasia (CIN) 1+. Secondary objectives were VE against virological and clinical endpoints associated with HPV‐16/18 and with high‐risk HPV types, immunogenicity and safety. Mean follow‐up for the according‐to‐protocol cohort for efficacy (ATP‐E) was ∼15 months after the third dose. In the ATP‐E (vaccine = 2,889; control = 2,894), for initially HPV DNA negative and seronegative subjects, HPV‐16/18 related VE (95% CI) was 94.2% (62.7, 99.9) against 6‐month PI and/or CIN1+ and 93.8% (60.2, 99.9) against cytological abnormalities. VE against HPV‐16/18 associated CIN1+ and CIN2+ was 100% (−50.4, 100) and 100% (−140.2, 100), respectively (no cases in the vaccine group and 4 CIN1+ and 3 CIN2+ cases in the control group). At Month 7, at least 99.7% of initially seronegative vaccine recipients had seroconverted for HPV‐16/18; geometric mean antibody titres (95% CI) were 6,996 (6,212 to 7,880) EU/mL for anti‐HPV‐16 and 3,309 (2,942 to 3,723) EU/mL for anti‐HPV‐18. Safety outcomes between groups were generally similar. The HPV‐16/18 AS04‐adjuvanted vaccine is effective, immunogenic and has a clinically acceptable safety profile in young Chinese women. Prophylactic HPV vaccination has the potential to substantially reduce the burden of cervical cancer in China. What's New? With an estimated 75,000 new cases and 34,000 women dying from the disease annually, cervical cancer is a major public‐health concern in China. This is the first large scale randomised clinical trial of a human papillomavirus (HPV) vaccine in China. The vaccine was found to be effective, immunogenic, and to have a clinically acceptable safety profile in young Chinese women. Prophylactic HPV vaccination thus has the potential to substantially reduce the burden of cervical cancers and precancers in China.
Bibliography:Other authors from the HPV‐039 study group who have contributed to the study and the review and approval of the article: Yong Chen, Yejiang Zhu (Binhai CDC). Shang‐ying Hu, Feng Chen, Bin Liu, Jian‐feng Cui, Xin‐fu Liu, Unench Sharnuud and Wen‐hua Zhang (CICAMS). Xiao‐Li Cui (Shenyang Fourth People's Hospital, Shenyang city, Liaoning Province). Hongxing Pan (Jiangsu Province CDC). Haihua Le, Changrong Wang (Jintan CDC). Shiyin Xue, Jiahong Zhu (Lianshui CDC). Yong Chen, Ling Ling Shen (Xuzhou CDC).
and declare that their respective institutions received clinical trial funding from the GlaxoSmithKline group of companies, through the Jiangsu Province CDC, the CICAMS (Beijing, China) and the National Institutes for Food and Drug Control (NIFDC) (Beijing, China). F. Zhu, F. Zhao, Y. Hu received support for travel to meetings related to the study from the GlaxoSmithKline group of companies. H. Tang, H. Zhang, M. Lebacq, M.‐P. David, S. Datta, F. Struyf, D. Bi and D. Descamps are employees of the GlaxoSmithKline group of companies. H. Tang, M.‐P. David, S. Datta, F. Struyf, D. Bi and D. Descamps hold restricted shares and/or stock options from the GlaxoSmithKline group of companies.
Conflict of Interest
All authors have completed the Unified Competing Interest form at
Contributors
http://www.icmje.org/coi_disclosure.pdf
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Conflict of Interest: All authors have completed the Unified Competing Interest form at http://www.icmje.org/coi_disclosure.pdf and declare that their respective institutions received clinical trial funding from the GlaxoSmithKline group of companies, through the Jiangsu Province CDC, the CICAMS (Beijing, China) and the National Institutes for Food and Drug Control (NIFDC) (Beijing, China). F. Zhu, F. Zhao, Y. Hu received support for travel to meetings related to the study from the GlaxoSmithKline group of companies. H. Tang, H. Zhang, M. Lebacq, M.-P. David, S. Datta, F. Struyf, D. Bi and D. Descamps are employees of the GlaxoSmithKline group of companies. H. Tang, M.-P. David, S. Datta, F. Struyf, D. Bi and D. Descamps hold restricted shares and/or stock options from the GlaxoSmithKline group of companies.
Grant sponsor: This work was supported by GlaxoSmithKline Vaccines (registered as GlaxoSmithKline Biologicals SA). GlaxoSmithKline Vaccines designed the study in collaboration with investigators and coordinated gathering, analysis and interpretation of data and writing of the report. Investigators from the HPV-039 study group gathered data for the trial and cared for the women. All authors had full access to the complete final study report and had final responsibility for the decision to submit for publication. The manuscript was developed and coordinated by the authors in collaboration with an independent medical writer and a publication manager, both working on behalf of GlaxoSmithKline Vaccines.
Contributors: Other authors from the HPV-039 study group who have contributed to the study and the review and approval of the article: Yong Chen, Yejiang Zhu (Binhai CDC). Shang-ying Hu, Feng Chen, Bin Liu, Jian-feng Cui, Xin-fu Liu, Unench Sharnuud and Wen-hua Zhang (CICAMS). Xiao-Li Cui (Shenyang Fourth People's Hospital, Shenyang city, Liaoning Province). Hongxing Pan (Jiangsu Province CDC). Haihua Le, Changrong Wang (Jintan CDC). Shiyin Xue, Jiahong Zhu (Lianshui CDC). Yong Chen, Ling Ling Shen (Xuzhou CDC).
ISSN:0020-7136
1097-0215
1097-0215
DOI:10.1002/ijc.28897