Applied Tumor Biology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
Department of Reproductive Health, School of Medicine, College of Health Sciences, Moi University, Eldoret, Kenya.
Int J Cancer. 2024 Oct 1;155(7):1257-1267. doi: 10.1002/ijc.35036. Epub 2024 May 27.
While the incidence of cervical cancer has dropped in high-income countries due to organized cytology-based screening programs, it remains the leading cause of cancer death among women in Eastern Africa. Therefore, the World Health Organization (WHO) now urges providers to transition from widely prevalent but low-performance visual inspection with acetic acid (VIA) screening to primary human papillomavirus (HPV) DNA testing. Due to high HPV prevalence, effective triage tests are needed to identify those lesions likely to progress and so avoid over-treatment. To identify the optimal cost-effective strategy, we compared the VIA screen-and-treat approach to primary HPV DNA testing with p16/Ki67 dual-stain cytology or VIA as triage. We used a Markov model to calculate the budget impact of each strategy with incremental quality-adjusted life years and incremental cost-effectiveness ratios (ICER) as the main outcome. Deterministic cost-effectiveness analyses show that the screen-and-treat approach is highly cost-effective (ICER 2469 Int$), while screen, triage, and treat with dual staining is the most effective with favorable ICER than triage with VIA (ICER 9943 Int$ compared with 13,177 Int$). One-way sensitivity analyses show that the results are most sensitive to discounting, VIA performance, and test prices. In the probabilistic sensitivity analyses, the triage option using dual stain is the optimal choice above a willingness to pay threshold of 7115 Int$ being cost-effective as per WHO standards. The result of our analysis favors the use of dual staining over VIA as triage in HPV-positive women and portends future opportunities and necessary research to improve the coverage and acceptability of cervical cancer screening programs.
尽管由于有组织的细胞学筛查计划,高收入国家的宫颈癌发病率有所下降,但它仍是东非地区女性癌症死亡的主要原因。因此,世界卫生组织(WHO)现在敦促医疗服务提供者将广泛应用但性能较低的醋酸视觉检查(VIA)筛查方法转变为主要的人乳头瘤病毒(HPV)DNA 检测方法。由于 HPV 感染率较高,需要有效的分流检测来识别可能进展的病变,从而避免过度治疗。为了确定最佳的具有成本效益的策略,我们将 VIA 筛查-治疗方法与主要 HPV DNA 检测、p16/Ki67 双重染色细胞学检查或 VIA 作为分流方法进行了比较。我们使用马尔可夫模型来计算每种策略的预算影响,增量质量调整生命年和增量成本效益比(ICER)是主要的结果。确定性成本效益分析表明,筛查-治疗方法具有很高的成本效益(ICER 为 2469 国际元),而筛查、分流和双重染色治疗是最有效的方法,其 ICER 优于 VIA 分流(ICER 为 9943 国际元,而不是 13177 国际元)。单因素敏感性分析表明,结果对贴现、VIA 性能和检测价格最为敏感。在概率敏感性分析中,使用双重染色的分流选择在愿意支付的阈值 7115 国际元以上是符合成本效益的,符合世卫组织的标准。我们的分析结果有利于在 HPV 阳性女性中使用双重染色而非 VIA 作为分流方法,这预示着未来有机会和必要的研究来提高宫颈癌筛查计划的覆盖率和可接受性。