Van Effelterre Thierry P, Hogea Cosmina, Taylor Sylvia M
a GSK Vaccines; Global Epidemiology ; Wavre , Belgium.
b GSK Vaccines; Global Epidemiology ; King of Prussia , PA USA.
Hum Vaccin Immunother. 2016;12(1):8-19. doi: 10.1080/21645515.2015.1054584.
We developed a dynamic compartmental model to assess the impact of HPV Universal Mass Vaccination (UMV) with Cervarix™, which offers protection against HPV16/18 and cross-protection against other cancer-causing types, using up-to-date efficacy data. Analyses were performed in the UK because of the large amount of high quality epidemiological data available. For each HPV type/group of types considered, the model was calibrated to 14 epidemiological datasets (prevalence of HPV infection, cervical intraepithelial neoplasia (CIN): CIN1, CIN2, CIN3 pre-screening and cervical cancer (CC) incidence over 10 y post-screening). Impacts of cross-protection, female catch-up vaccination, and additional male vaccination on oncogenic infections, high-grade CIN (CIN2+) and CC were evaluated. Our results show that female UMV with 80% coverage and cross-protection against high-risk types resulted in 81% CIN2+ and 88% CC reductions vs. 57% and 75%, respectively, without cross-protection. Vaccinating 40% of males and 80% of females was equivalent to 90% female-only coverage regarding CIN2+ (87% and 87%, respectively) and CC (93% and 94%, respectively) reductions. Female-only coverage of 80% substantially reduced male HPV16 and 18 infection due to herd protection (74% and 89%, respectively). Increasing female coverage to 90% reduced HPV16 and HPV18 infections in males relatively similarly to 80% female combined with 40% male coverage. Model outcomes strengthen previous conclusions about the significant added value of Cervarix™ cross-protection for CC prevention, the primary HPV vaccination public health priority. Regarding female CC prevention and male HPV16/18 infection, small increases in female coverage induce similar benefits to those achieved by additionally vaccinating men with 40% coverage.
我们开发了一种动态分区模型,利用最新的疗效数据,评估使用希瑞适(Cervarix™)进行人乳头瘤病毒(HPV)全民大规模疫苗接种(UMV)的影响,希瑞适可预防HPV16/18,并对其他致癌类型提供交叉保护。由于英国有大量高质量的流行病学数据,因此在英国进行了分析。对于每种考虑的HPV类型/类型组,该模型根据14个流行病学数据集(HPV感染患病率、宫颈上皮内瘤变(CIN):CIN1、CIN2、CIN3筛查前以及筛查后10年宫颈癌(CC)发病率)进行校准。评估了交叉保护、女性补种疫苗以及额外的男性疫苗接种对致癌感染、高级别CIN(CIN2+)和CC的影响。我们的结果表明,覆盖率为80%且对高危类型有交叉保护的女性UMV,与无交叉保护时相比,CIN2+和CC分别减少了81%和88%,而无交叉保护时分别为57%和75%。接种40%的男性和80%的女性,在CIN2+减少方面(分别为87%和87%)和CC减少方面(分别为93%和94%),等同于仅90%女性接种的覆盖率。仅80%的女性覆盖率由于群体保护大幅降低了男性HPV16和18感染(分别为74%和89%)。将女性覆盖率提高到90%,对男性HPV16和HPV18感染的降低效果,与80%女性加40%男性覆盖率的情况相对类似。模型结果强化了先前关于希瑞适交叉保护对预防CC具有显著附加价值的结论,CC预防是HPV疫苗接种首要的公共卫生重点。关于女性CC预防和男性HPV16/18感染,女性覆盖率的小幅提高所带来的益处,与额外接种40%覆盖率男性疫苗所取得的益处相似。