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

نویسندگان

  • Feng‐cai Zhu
  • Shang‐Ying Hu
  • Ying Hong
  • Yue‐Mei Hu
  • Xun Zhang
  • Yi‐Ju Zhang
  • Qin‐Jing Pan
  • Wen‐Hua Zhang
  • Fang‐Hui Zhao
  • Cheng‐Fu Zhang
  • Xiaoping Yang
  • Jia‐Xi Yu
  • Jiahong Zhu
  • Yejiang Zhu
  • Feng Chen
  • Qian Zhang
  • Hong Wang
  • Changrong Wang
  • Jun Bi
  • Shiyin Xue
  • Lingling Shen
  • Yan‐Shu Zhang
  • Yunkun He
  • Haiwen Tang
  • Naveen Karkada
  • Pemmaraju Suryakiran
  • Dan Bi
  • Frank Struyf
چکیده

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.

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عنوان ژورنال:

دوره 6  شماره 

صفحات  -

تاریخ انتشار 2017