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Efficacy, immunogenicity, and safety of the HPV‐16/18 AS04‐adjuvanted vaccine in Chinese women aged 18–25 years: event‐triggered analysis of a randomized controlled trial
We previously reported the results of a phase II/III, double‐blind, randomized controlled study in Chinese women (NCT00779766) showing a 94.2% (95% confidence interval: 62.7–99.9) HPV‐16/18 AS04‐adjuvanted vaccine efficacy (VE) against cervical intraepithelial neoplasia grade 1 or higher (CIN1+) and...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5269697/ https://www.ncbi.nlm.nih.gov/pubmed/27998015 http://dx.doi.org/10.1002/cam4.869 |
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author | Zhu, Feng‐cai Hu, Shang‐Ying Hong, Ying Hu, Yue‐Mei Zhang, Xun Zhang, Yi‐Ju Pan, Qin‐Jing Zhang, Wen‐Hua Zhao, Fang‐Hui Zhang, Cheng‐Fu Yang, Xiaoping Yu, Jia‐Xi Zhu, Jiahong Zhu, Yejiang Chen, Feng Zhang, Qian Wang, Hong Wang, Changrong Bi, Jun Xue, Shiyin Shen, Lingling Zhang, Yan‐Shu He, Yunkun Tang, Haiwen Karkada, Naveen Suryakiran, Pemmaraju Bi, Dan Struyf, Frank |
author_facet | Zhu, Feng‐cai Hu, Shang‐Ying Hong, Ying Hu, Yue‐Mei Zhang, Xun Zhang, Yi‐Ju Pan, Qin‐Jing Zhang, Wen‐Hua Zhao, Fang‐Hui Zhang, Cheng‐Fu Yang, Xiaoping Yu, Jia‐Xi Zhu, Jiahong Zhu, Yejiang Chen, Feng Zhang, Qian Wang, Hong Wang, Changrong Bi, Jun Xue, Shiyin Shen, Lingling Zhang, Yan‐Shu He, Yunkun Tang, Haiwen Karkada, Naveen Suryakiran, Pemmaraju Bi, Dan Struyf, Frank |
author_sort | Zhu, Feng‐cai |
collection | PubMed |
description | We previously reported the results of a phase II/III, double‐blind, randomized controlled study in Chinese women (NCT00779766) showing a 94.2% (95% confidence interval: 62.7–99.9) HPV‐16/18 AS04‐adjuvanted vaccine efficacy (VE) against cervical intraepithelial neoplasia grade 1 or higher (CIN1+) and/or 6‐month (M) persistent infection (PI) with a mean follow‐up of <2 years, and immunogenicity until 7 months post‐dose 1. Here, we report efficacy and safety results from an event‐triggered analysis with ~3 years longer follow‐up, and immunogenicity until M24. Healthy 18–25‐year‐old women (N = 6051) were randomized (1:1) to receive three doses of HPV‐16/18 vaccine or Al(OH)(3) (control) at M0, 1, 6. VE against HPV‐16/18‐associated CIN2+, and cross‐protective VE against infections with nonvaccine oncogenic HPV types, immunogenicity, and safety were assessed. In the according‐to‐protocol efficacy cohort, in initially seronegative/DNA‐negative women (vaccine group: N = 2524; control group: N = 2535), VE against HPV‐16/18‐associated CIN2+ was 87.3% (5.3–99.7); VE against incident infection or against 6‐month persistent infection associated with HPV‐31/33/45 was 50.1% (34.3–62.3) or 52.6% (24.5–70.9), respectively. At least, 99.6% of HPV‐16/18‐vaccines remained seropositive for anti‐HPV‐16/18 antibodies; anti‐HPV‐16 and ‐18 geometric mean titers were 1271.1 EU/mL (1135.8–1422.6) and 710.0 EU/ml (628.6–801.9), respectively. Serious adverse events were infrequent (1.7% vaccine group [N = 3026]; 2.5% control group [N = 3026]). Of the 1595 reported pregnancies, nine had congenital anomalies (five live infants, three elective terminations, one stillbirth) that were unlikely vaccination‐related (blinded data). VE against HPV‐16/18‐associated CIN2+ was demonstrated and evidence of cross‐protective VE against oncogenic HPV types was shown. The vaccine was immunogenic and had an acceptable safety profile. |
format | Online Article Text |
id | pubmed-5269697 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52696972017-02-01 Efficacy, immunogenicity, and safety of the HPV‐16/18 AS04‐adjuvanted vaccine in Chinese women aged 18–25 years: event‐triggered analysis of a randomized controlled trial Zhu, Feng‐cai Hu, Shang‐Ying Hong, Ying Hu, Yue‐Mei Zhang, Xun Zhang, Yi‐Ju Pan, Qin‐Jing Zhang, Wen‐Hua Zhao, Fang‐Hui Zhang, Cheng‐Fu Yang, Xiaoping Yu, Jia‐Xi Zhu, Jiahong Zhu, Yejiang Chen, Feng Zhang, Qian Wang, Hong Wang, Changrong Bi, Jun Xue, Shiyin Shen, Lingling Zhang, Yan‐Shu He, Yunkun Tang, Haiwen Karkada, Naveen Suryakiran, Pemmaraju Bi, Dan Struyf, Frank Cancer Med Clinical Cancer Research We previously reported the results of a phase II/III, double‐blind, randomized controlled study in Chinese women (NCT00779766) showing a 94.2% (95% confidence interval: 62.7–99.9) HPV‐16/18 AS04‐adjuvanted vaccine efficacy (VE) against cervical intraepithelial neoplasia grade 1 or higher (CIN1+) and/or 6‐month (M) persistent infection (PI) with a mean follow‐up of <2 years, and immunogenicity until 7 months post‐dose 1. Here, we report efficacy and safety results from an event‐triggered analysis with ~3 years longer follow‐up, and immunogenicity until M24. Healthy 18–25‐year‐old women (N = 6051) were randomized (1:1) to receive three doses of HPV‐16/18 vaccine or Al(OH)(3) (control) at M0, 1, 6. VE against HPV‐16/18‐associated CIN2+, and cross‐protective VE against infections with nonvaccine oncogenic HPV types, immunogenicity, and safety were assessed. In the according‐to‐protocol efficacy cohort, in initially seronegative/DNA‐negative women (vaccine group: N = 2524; control group: N = 2535), VE against HPV‐16/18‐associated CIN2+ was 87.3% (5.3–99.7); VE against incident infection or against 6‐month persistent infection associated with HPV‐31/33/45 was 50.1% (34.3–62.3) or 52.6% (24.5–70.9), respectively. At least, 99.6% of HPV‐16/18‐vaccines remained seropositive for anti‐HPV‐16/18 antibodies; anti‐HPV‐16 and ‐18 geometric mean titers were 1271.1 EU/mL (1135.8–1422.6) and 710.0 EU/ml (628.6–801.9), respectively. Serious adverse events were infrequent (1.7% vaccine group [N = 3026]; 2.5% control group [N = 3026]). Of the 1595 reported pregnancies, nine had congenital anomalies (five live infants, three elective terminations, one stillbirth) that were unlikely vaccination‐related (blinded data). VE against HPV‐16/18‐associated CIN2+ was demonstrated and evidence of cross‐protective VE against oncogenic HPV types was shown. The vaccine was immunogenic and had an acceptable safety profile. John Wiley and Sons Inc. 2016-12-20 /pmc/articles/PMC5269697/ /pubmed/27998015 http://dx.doi.org/10.1002/cam4.869 Text en © 2016 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Cancer Research Zhu, Feng‐cai Hu, Shang‐Ying Hong, Ying Hu, Yue‐Mei Zhang, Xun Zhang, Yi‐Ju Pan, Qin‐Jing Zhang, Wen‐Hua Zhao, Fang‐Hui Zhang, Cheng‐Fu Yang, Xiaoping Yu, Jia‐Xi Zhu, Jiahong Zhu, Yejiang Chen, Feng Zhang, Qian Wang, Hong Wang, Changrong Bi, Jun Xue, Shiyin Shen, Lingling Zhang, Yan‐Shu He, Yunkun Tang, Haiwen Karkada, Naveen Suryakiran, Pemmaraju Bi, Dan Struyf, Frank Efficacy, immunogenicity, and safety of the HPV‐16/18 AS04‐adjuvanted vaccine in Chinese women aged 18–25 years: event‐triggered analysis of a randomized controlled trial |
title | Efficacy, immunogenicity, and safety of the HPV‐16/18 AS04‐adjuvanted vaccine in Chinese women aged 18–25 years: event‐triggered analysis of a randomized controlled trial |
title_full | Efficacy, immunogenicity, and safety of the HPV‐16/18 AS04‐adjuvanted vaccine in Chinese women aged 18–25 years: event‐triggered analysis of a randomized controlled trial |
title_fullStr | Efficacy, immunogenicity, and safety of the HPV‐16/18 AS04‐adjuvanted vaccine in Chinese women aged 18–25 years: event‐triggered analysis of a randomized controlled trial |
title_full_unstemmed | Efficacy, immunogenicity, and safety of the HPV‐16/18 AS04‐adjuvanted vaccine in Chinese women aged 18–25 years: event‐triggered analysis of a randomized controlled trial |
title_short | Efficacy, immunogenicity, and safety of the HPV‐16/18 AS04‐adjuvanted vaccine in Chinese women aged 18–25 years: event‐triggered analysis of a randomized controlled trial |
title_sort | efficacy, immunogenicity, and safety of the hpv‐16/18 as04‐adjuvanted vaccine in chinese women aged 18–25 years: event‐triggered analysis of a randomized controlled trial |
topic | Clinical Cancer Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5269697/ https://www.ncbi.nlm.nih.gov/pubmed/27998015 http://dx.doi.org/10.1002/cam4.869 |
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