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九价人乳头瘤病毒疫苗:临床开发项目综述。

9-Valent human papillomavirus vaccine: a review of the clinical development program.

机构信息

a Merck & Co., Inc ., Kenilworth , NJ , USA.

出版信息

Expert Rev Vaccines. 2017 Nov;16(11):1119-1139. doi: 10.1080/14760584.2017.1383158. Epub 2017 Oct 9.

Abstract

The 9-valent human papillomavirus (9vHPV) vaccine covers the same HPV types (6/11/16/18) as the quadrivalent HPV (qHPV) vaccine and 5 additional cancer-causing types (31/33/45/52/58). Epidemiological studies indicate that the 9vHPV vaccine could prevent approximately 90% of cervical cancers, 70-85% of high-grade cervical dysplasia (precancers), 85-95% of HPV-related vulvar, vaginal, and anal cancers, and 90% of genital warts. Areas covered: Study design features and key findings from the 9vHPV vaccine clinical development program are reviewed. In particular, 9vHPV vaccine efficacy was established in a Phase III study in young women age 16-26 years. Efficacy results in young women were extrapolated to pre- and young adolescent girls and boys and young men by immunological bridging (i.e., demonstration of non-inferior immunogenicity in these groups versus young women). Expert commentary: The development of the 9vHPV vaccine is the outcome of 20 years of continuous clinical research. Broad vaccination programs could help substantially decrease the incidence of HPV-related disease.

摘要

九价人乳头瘤病毒(9vHPV)疫苗涵盖了与四价 HPV(qHPV)疫苗相同的 HPV 类型(6/11/16/18),以及另外 5 种致癌类型(31/33/45/52/58)。流行病学研究表明,9vHPV 疫苗可预防约 90%的宫颈癌、70-85%的高级别宫颈上皮内瘤变(癌前病变)、85-95%的 HPV 相关外阴癌、阴道癌和肛门癌,以及 90%的生殖器疣。涵盖领域:本文回顾了 9vHPV 疫苗临床开发计划的研究设计特点和主要发现。特别是,在年龄为 16-26 岁的年轻女性中开展的 III 期研究证实了 9vHPV 疫苗的疗效。通过免疫桥接(即在这些组与年轻女性相比,免疫原性非劣效性的证明)将年轻女性的疗效结果外推至青春期前和青春期少女和男孩以及年轻男性。专家评论:9vHPV 疫苗的开发是 20 年持续临床研究的结果。广泛的疫苗接种计划可以大大降低 HPV 相关疾病的发病率。

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