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AS04 佐剂 HPV-16/18 疫苗在减少年轻女性口咽 HPV 感染中的效果 - 来自社区随机试验的结果。

Effectiveness of the AS04-adjuvanted HPV-16/18 vaccine in reducing oropharyngeal HPV infections in young females-Results from a community-randomized trial.

机构信息

Department of Infections and Cancer, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Department of Laboratory Medicine, Karolinska Institute, Stockholm, Sweden.

出版信息

Int J Cancer. 2020 Jul 1;147(1):170-174. doi: 10.1002/ijc.32791. Epub 2019 Dec 14.

DOI:10.1002/ijc.32791
PMID:31736068
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7318585/
Abstract

We studied effectiveness of the AS04-adjuvanted HPV-16/18 (AS04-HPV-16/18) vaccine against human papillomavirus (HPV) oropharyngeal infections associated with the increase of head/neck cancers in western countries. All 38,631 resident adolescents from 1994 to 1995 birth cohorts of 33 Finnish communities were invited in this community-randomized trial (NCT00534638). During 2008-2009, 11,275 girls and 6,129 boys were enrolled in three arms of 11 communities each. In Arm A, 90% of vaccinated girls/boys, and in Arm B, 90% of vaccinated girls received AS04-HPV-16/18 vaccine. Other Arm A/B and all Arm C vaccinated participants received control vaccine. All Arm A participants and Arm B female participants were blinded to vaccine allocation. Oropharyngeal samples were analyzed from 4,871 18.5-year-old females who attended follow-up visit 3-6 years postvaccination. HPV DNA prevalence was determined by SPF-10 LiPA and Multiplex type-specific PCR. Total vaccine effectiveness (VE) was defined as relative reduction of oropharyngeal HPV prevalence in pooled Arms A/B HPV-vaccinated females vs. all Arm C females. VE against oropharyngeal HPV-16/18, HPV-31/45 and HPV-31/33/45 infections were 82.4% (95% confidence intervals [CI]: 47.3-94.1), 75.3% (95%CI: 12.7-93.0) and 69.9% (95% CI: 29.6-87.1), respectively. In conclusion, the AS04-HPV-16/18 vaccine showed effectiveness against vaccine and nonvaccine HPV-types oropharyngeal infections in adolescent females up to 6 years postvaccination.

摘要

我们研究了 AS04 佐剂 HPV-16/18(AS04-HPV-16/18)疫苗对与西方国家头颈部癌症增加相关的人乳头瘤病毒(HPV)口咽感染的有效性。所有 38631 名来自 1994 年至 1995 年出生队列的芬兰社区居民青少年都被邀请参加这项社区随机试验(NCT00534638)。在 2008-2009 年期间,11 个社区的每个社区招募了 11 个组中的 11275 名女孩和 6129 名男孩。在 A 臂中,90%接种疫苗的女孩/男孩,以及在 B 臂中,90%接种疫苗的女孩接受了 AS04-HPV-16/18 疫苗。其他 A 臂/B 臂和所有 C 臂接种的参与者接受了对照疫苗。所有 A 臂参与者和 B 臂女性参与者对疫苗分配均不知情。对 4871 名 18.5 岁的女性进行了口咽样本分析,这些女性在接种疫苗后 3-6 年参加了随访。通过 SPF-10 LiPA 和多重型特异性 PCR 分析 HPV DNA 流行率。总疫苗有效性(VE)定义为 A 臂/B 臂 HPV 疫苗接种女性的口咽 HPV 流行率相对于所有 C 臂女性的相对降低。针对口咽 HPV-16/18、HPV-31/45 和 HPV-31/33/45 感染的 VE 分别为 82.4%(95%CI:47.3-94.1)、75.3%(95%CI:12.7-93.0)和 69.9%(95%CI:29.6-87.1)。总之,AS04-HPV-16/18 疫苗在接种疫苗后的 6 年内对青少年女性的疫苗和非疫苗 HPV 型口咽感染具有有效性。

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