de Bondt Daniël D, Jansen Erik E L, Stogios Christine, McCurdy Bronwen R, Kupets Rachel, Murphy Joan, Costescu Dustin, Rabeneck Linda, Truscott Rebecca, Hontelez Jan A C, de Kok Inge M C M
Department of Public Health, Erasmus Medical Center Rotterdam, Rotterdam, The Netherlands.
Ontario Health (Cancer Care Ontario), Toronto, ON, Canada.
Med Decis Making. 2025 Jul;45(5):545-556. doi: 10.1177/0272989X251332597. Epub 2025 Apr 22.
ObjectivesIn Ontario, Canada, the first cohorts who were offered school-based human papillomavirus (HPV) vaccination are now eligible for cervical screening. We determined which screening strategies for these populations would result in optimal harms-benefits ratios of screening.MethodsWe used the hybrid microsimulation model STDSIM- MISCAN-Cervix to determine the harms and cancers prevented of 309 different primary HPV screening strategies, varying by screening ages and triage methods. In addition, we performed an unstratified (i.e., uniform screening protocols) and stratified (i.e., screening protocols by vaccination status) analysis. Harms induced were quantified as a weighted combination of the number of primary HPV-based screens and colposcopy referrals at 1:10. A harms-benefit acceptability threshold of number of harms induced for each cancer prevented was set at the estimated ratio under current screening recommendations in unvaccinated cohorts in Ontario.ResultsFor the unstratified scenario, 5 lifetime screens with HPV16/18 genotyping was optimal. For the stratified scenario, the optimal scenario was 3 lifetime screens with HPV16/18/31/33/45/52/58 genotyping for vaccinated individuals versus 6 lifetime screens with HPV16/18 genotyping for unvaccinated individuals.ConclusionsWe determined the optimal cervical screening strategy in Ontario over the next decades. To maintain an optimal harms-benefits balance of screening, the Ontario Cervical Screening Program could adjust screening recommendations in the future to reduce the number of lifetime screens and extend screening intervals to account for vaccinated cohorts. Stratified screening by vaccination status could further improve this balance on an individual level.HighlightsPeople in cohorts who were offered HPV vaccination as part of Ontario's school-based program may achieve a better harms-benefits balance if cervical screening recommendations are updated to a less intensive protocol in future. This holds for the cohorts as a whole (i.e., unstratified screening) as well as for both vaccinated and unvaccinated individuals in these cohorts.Instead of using a cost-effectiveness threshold, it is possible to determine optimal screening protocols by calculating an acceptability threshold using alternative harms-benefits measures based on existing policy.Using univariate harms measures such as primary HPV screening tests or colposcopies per 1,000 people can yield biases in optimizing cervical screening programs. Alternatively, combining both primary screens and colposcopy referrals could provide a more accurate harms measure and result in optimal strategies with a better balance between harms and benefits.
目标
在加拿大安大略省,首批接受基于学校的人乳头瘤病毒(HPV)疫苗接种的人群现在有资格进行宫颈癌筛查。我们确定了针对这些人群的哪些筛查策略将产生最佳的筛查危害 - 益处比。
方法
我们使用混合微观模拟模型STDSIM - MISCAN - Cervix来确定309种不同的主要HPV筛查策略的危害和预防的癌症数量,这些策略因筛查年龄和分流方法而异。此外,我们进行了非分层(即统一筛查方案)和分层(即按疫苗接种状态的筛查方案)分析。所诱导的危害被量化为基于HPV的初次筛查数量和阴道镜转诊数量按1:10的加权组合。在安大略省未接种疫苗人群的当前筛查建议下,为每种预防的癌症所诱导的危害数量设定了一个危害 - 益处可接受阈值。
结果
对于非分层情况,5次终身HPV16/18基因分型筛查是最佳的。对于分层情况,最佳方案是接种疫苗的个体进行3次终身HPV16/18/31/33/45/52/5十八基因分型筛查,而未接种疫苗的个体进行6次终身HPV16/18基因分型筛查。
结论
我们确定了安大略省未来几十年的最佳宫颈癌筛查策略。为了保持筛查的最佳危害 - 益处平衡,安大略省宫颈癌筛查计划未来可以调整筛查建议,以减少终身筛查次数并延长筛查间隔,以考虑接种疫苗的人群。按疫苗接种状态进行分层筛查可以在个体层面进一步改善这种平衡。
要点
如果未来将宫颈癌筛查建议更新为强度较低的方案,作为安大略省基于学校计划一部分接受HPV疫苗接种人群中的人们可能会实现更好的危害 - 益处平衡。这适用于整个队列(即非分层筛查)以及这些队列中接种疫苗和未接种疫苗的个体。
不用成本效益阈值,而是可以通过基于现有政策使用替代的危害 - 益处措施计算可接受阈值来确定最佳筛查方案。
使用单变量危害措施,如每1000人的初次HPV筛查测试或阴道镜检查,在优化宫颈癌筛查计划时可能会产生偏差。或者,将初次筛查和阴道镜转诊结合起来可以提供更准确的危害衡量,并导致在危害和益处之间具有更好平衡的最佳策略。