Burger Emily A, Kim Jane J, Sy Stephen, Castle Philip E
Harvard T.H. Chan School of Public Health, Center for Health Decision Science, Boston, Massachusetts.
University of Oslo, Department of Health Management and Health Economics, Oslo, Norway.
Clin Infect Dis. 2017 Sep 15;65(6):893-899. doi: 10.1093/cid/cix475.
Although new human papillomavirus (HPV) infections can occur at all ages, the age at which women acquire their "causal" HPV infection that develops into cervical cancer is poorly understood and practically unobservable. We aimed to estimate the age distribution at which individuals acquired their causal HPV infection in the absence of HPV vaccination or screening to help guide the optimal use of both.
Using an empirically calibrated mathematical model that simulates the natural history of cervical cancer, we estimated the cumulative number of causal HPV infections by age, stratified by HPV genotype (HPV16 vs. other HPV genotypes), and the direct age-specific reduction in cancer incidence for alternative vaccination initiation scenarios (i.e., age 9-45 years).
Our model projected that among all cervical cancers, 50% and 75% of women acquired their causal HPV infection by ages 20.6 (range: 20.1-21.1) and 30.6 (range: 29.6-31.6) years, respectively. HPV16 infections were acquired at an earlier age. Assuming 95% efficacy against HPV16 and HPV18 infections, the direct reduction in lifetime risk of cervical cancer varied from 55% (53-56%) among women vaccinated at age 9 years to 6% (range: 6-7%) among women vaccinated at age 45 years. Similar patterns were observed for the second-generation vaccine.
Although new HPV infections and precancers can occur throughout a woman's lifetime, only a small proportion are acquired in mid-adult women and are vaccine-preventable. Our simulations highlight the potential limitations of using surrogate endpoints for vaccine efficacy studies of mid-adult women to guide policy decisions for implementation.
尽管新的人乳头瘤病毒(HPV)感染可发生于所有年龄段,但对于女性感染导致宫颈癌的“致病性”HPV的年龄,人们了解甚少,且实际上无法观察到。我们旨在估计在未接种HPV疫苗或未进行筛查的情况下,个体感染致病性HPV的年龄分布,以帮助指导两者的最佳使用。
使用一个经过经验校准的数学模型来模拟宫颈癌的自然史,我们按年龄、HPV基因型(HPV16与其他HPV基因型)分层,估计致病性HPV感染的累积数量,以及在不同的疫苗接种起始方案(即9至45岁)下,特定年龄对癌症发病率的直接降低情况。
我们的模型预测,在所有宫颈癌病例中,分别有50%和75%的女性在20.6岁(范围:20.1至21.1岁)和30.6岁(范围:29.6至31.6岁)时感染了致病性HPV。HPV16感染的发生年龄更早。假设疫苗对HPV16和HPV18感染的效力为95%,宫颈癌终身风险的直接降低幅度在9岁接种疫苗的女性中为55%(53%至56%),在45岁接种疫苗的女性中为6%(范围:6%至7%)。第二代疫苗也观察到类似模式。
尽管新的HPV感染和癌前病变可在女性一生中随时发生,但只有一小部分是成年中期女性感染的,且可通过疫苗预防。我们的模拟突出了在疫苗效力研究中使用替代终点来指导成年中期女性的疫苗接种政策决策的潜在局限性。