Community intervention of a single-dose or 2-dose regimen of bivalent human papillomavirus vaccine in schoolgirls in Thailand: vaccine effectiveness 2 years and 4 years after vaccination.

Suchada Jiamsiri, Chulwoo Rhee, Hyeon Seon Ahn, Hyeong-Won Seo, Worrawan Klinsupa, Sunju Park, Jinae Lee, Nakorn Premsri, Chawetsan Namwat, Patummal Silaporn, Jean-Louis Excler, Deok-Ryun Kim, Yun Chon, Joshua N Sampson, Pornjarim Nilyanimit, Sompong Vongpunsawad, Nimesh Poudyal, Lauri E Markowitz, Gitika Panicker, Elizabeth R Unger, Supachai Rerks-Ngarm, Yong Poovorawan, Julia Lynch
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Abstract

Background: With accumulating evidence of single-dose human papillomavirus (HPV) vaccine efficacy in young women, we conducted a community vaccine effectiveness study comparing HPV single-dose and 2-dose regimens (0 and 6 months) of a bivalent HPV vaccine among grade 8 schoolgirls (aged 13-14 years) in Thailand.

Methods: In 2018, eligible grade 8 schoolgirls in Udon Thani (single dose) and Buri Ram (2 doses) provinces were offered HPV vaccine per assigned dose regimen. Concurrently, a cross-sectional survey for measuring baseline HPV prevalence was conducted in grade 10 (n = 2600) and grade 12 unvaccinated schoolgirls (n = 2000) in each province. HPV infection was assessed in first-void urine samples, tested by DNA polymerase chain reaction on the cobas 4800 system (Roche Molecular Diagnostics, Pleasanton, CA). All samples positive on the cobas system and an equal number of negative samples were also tested by Anyplex II HPV28 Detection (Seegene, Seoul, South Korea). The surveys were repeated in 2020 and 2022, when vaccinated grade 8 schoolgirls reached grade 10, and then subsequently grade 12, respectively. Vaccine effectiveness was estimated by comparing the weighted prevalence of HPV-16 or HPV-18 between grade-matched unvaccinated schoolgirls on the baseline survey (2018) and vaccinated schoolgirls in the year-2 (2020) and year-4 (2022) surveys. Adjustment methods were used in the analysis to account for potential differences in sexual behavior due to the noncontemporaneous comparison.

Results: The prevalence of HPV-16 and HPV-18 on the baseline survey among unvaccinated grade 10/grade 12 schoolgirls was 2.90% (95% confidence interval [CI] = 2.54% to 3.31%)/3.98% (95% CI = 3.52% to 4.49%) for Udon Thani and 3.87% (95% CI = 3.46% to 4.34%)/6.13% (95% CI = 5.56% to 6.75%) for Buri Ram. On the year-2 survey, the prevalence among vaccinated grade 10 schoolgirls was 0.57% (95% CI = 0.42% to 0.77%) for Udon Thani and 0.31% (95% CI = 0.21% to 0.47%) for Buri Ram. The 2-year postvaccination crude vaccine effectiveness for the single-dose regimen was estimated at 80.4% (95% CI = 73.9% to 86.9%), and for the 2-dose regimen at 91.9% (95% CI = 88.5% to 95.4%). On the year-4 survey, the prevalence among vaccinated grade 12 schoolgirls was 0.37% (95% CI = 0.25% to 0.56%) for Udon Thani and 0.28% (95% CI = 0.18% to 0.45%) for Buri Ram. Four-year postvaccination crude vaccine effectiveness for the single-dose regimen was estimated at 90.6% (95% CI = 86.6% to 94.6%) and for the 2-dose regimen was estimated at 95.4% (95% CI = 93.2% to 97.6%). All adjustment methods minimally affected vaccine effectiveness for the single-dose and 2-dose regimens. At 4 years after vaccination, the difference in crude vaccine effectiveness between the single-dose and 2-dose regimens was ‒4.79% (95% CI = ‒9.32% to ‒0.25%), meeting the study's noninferiority criteria.

Conclusions: Our study demonstrated that both single-dose and 2-dose HPV vaccination significantly decreased HPV-16/18 point prevalence 2 years and 4 years after vaccination. Crude vaccine effectiveness at 4 years after vaccination was greater than 90% for both the single-dose and 2-dose regimens; the single-dose regimen was not inferior to the 2-dose regimen. These data show that a single dose of HPV vaccine provides high levels of protection when administered to schoolgirls younger than 15 years of age.

泰国女学生接种二价人类乳头瘤病毒疫苗单剂或两剂方案的社区干预:疫苗接种后 2 年和 4 年的效果。
背景:随着单剂量人乳头瘤病毒(HPV)疫苗在年轻女性中疗效的证据不断积累,我们在泰国八年级女生(13-14 岁)中开展了一项社区疫苗疗效研究,比较了二价 HPV 疫苗的单剂量和二剂量方案(0 个月和 6 个月):2018年,乌隆府(单剂)和武里南府(2剂)符合条件的8年级女生按指定剂量方案接种了HPV疫苗。与此同时,还对各省 10 年级(2600 人)和 12 年级未接种疫苗的女学生(2000 人)进行了横断面调查,以测量 HPV 的基线流行率。通过 DNA 聚合酶链反应在 cobas 4800 系统(罗氏分子诊断公司,加利福尼亚州普莱森顿)上检测第一次排出的尿液样本,评估 HPV 感染情况。所有在 cobas 系统上呈阳性的样本和同等数量的阴性样本也通过 Anyplex II HPV28 检测器(Seegene,韩国首尔)进行检测。分别在 2020 年和 2022 年,即接种疫苗的八年级女生升入十年级和十二年级时,再次进行调查。通过比较基线调查(2018 年)中未接种疫苗的年级匹配女学生与第 2 年(2020 年)和第 4 年(2022 年)调查中接种疫苗的女学生之间的 HPV-16 或 HPV-18 加权流行率,估算疫苗效果。分析中使用了调整方法,以考虑非同期比较导致的性行为的潜在差异:在基线调查中,未接种疫苗的 10 年级/12 年级女生的 HPV-16 和 HPV-18 感染率分别为:乌隆府 2.90%(95% 置信区间 [CI] = 2.54% 至 3.31%)/3.98%(95% CI = 3.52% 至 4.49%),武里府 3.87%(95% CI = 3.46% 至 4.34%)/6.13%(95% CI = 5.56% 至 6.75%)。在第 2 年的调查中,乌隆他尼府 10 年级女学生的疫苗接种率为 0.57%(95% CI = 0.42% 至 0.77%),布里拉姆府为 0.31%(95% CI = 0.21% 至 0.47%)。接种后 2 年,单剂方案的粗疫苗效力估计为 80.4% (95% CI = 73.9% 至 86.9%),双剂方案的粗疫苗效力估计为 91.9% (95% CI = 88.5% 至 95.4%)。在第 4 年的调查中,乌隆他尼的 12 年级女生接种率为 0.37%(95% CI = 0.25% 到 0.56%),武里南的接种率为 0.28%(95% CI = 0.18% 到 0.45%)。接种后四年,单剂方案的粗疫苗效力估计为 90.6% (95% CI = 86.6% 至 94.6%),双剂方案的粗疫苗效力估计为 95.4% (95% CI = 93.2% 至 97.6%)。所有调整方法对单剂和双剂方案的疫苗效力影响都很小。接种4年后,单剂量和双剂量方案的粗疫苗效力差异为-4.79%(95% CI = -9.32%至-0.25%),符合研究的非劣效性标准:我们的研究表明,接种单剂和两剂HPV疫苗均能显著降低接种后2年和4年的HPV-16/18点流行率。接种后 4 年,单剂和双剂方案的粗疫苗有效率均大于 90%;单剂方案不劣于双剂方案。这些数据表明,为 15 岁以下的女学生接种单剂 HPV 疫苗可提供高水平的保护。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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