Deshmukh Ashish A, Chiao Elizabeth Y, Das Prajnan, Cantor Scott B
Cancer Prevention Training Research Program, The University of Texas MD Anderson Cancer Center, Houston, TX, United States; Department of Health Services Research, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Department of Medicine, Section of Infectious Diseases, Baylor College of Medicine, Houston, TX, United States.
Vaccine. 2014 Dec 5;32(51):6941-6947. doi: 10.1016/j.vaccine.2014.10.052. Epub 2014 Nov 1.
We examined the long-term clinical and economic benefits of quadrivalent human papillomavirus (qHPV) vaccine as a secondary/adjunct prevention strategy in the prevention of recurrent high-grade intraepithelial neoplasia (HGAIN) in HIV-negative men who have sex with men (MSM) and are 27 years or older. We constructed a Markov model to evaluate the clinical effectiveness and cost-effectiveness of two strategies: (1) no qHPV vaccine after treatment for HGAIN versus (2) qHPV vaccine after treatment for HGAIN. Model parameters, including natural history of anal cancer, vaccine efficacy measured in terms of hazard ratio (HR) (decrease in the risk of recurrent HGAIN), HGAIN treatment efficacy, utilities, and costs, were obtained from the literature. The outcomes were measured in terms of lifetime risk of anal cancer, lifetime cost, quality-adjusted life years, and incremental cost-effectiveness ratios (ICERs). Sensitivity analysis was conducted on all model parameters. We found that vaccinating HIV-negative MSM reduced the lifetime risk of anal cancer by 60.77% at an ICER of US$87,240 per quality-adjusted life-year. The results were highly sensitive to vaccine efficacy, transition of HGAIN to anal cancer, cost of treatment for HGAIN, vaccine degree of protection over time, and the vaccine duration of protection and less sensitive to HPV clearance, cost of qHPV vaccine, and the transitions from normal to low-grade anal intraepithelial neoplasia (LGAIN) and normal to HGAIN. With an HR of 0.3, the ICER was well below a $50,000 willingness-to-pay threshold; with an HR of 0.5, the ICER was still below a threshold of $100,000. The most critical disease-related factor influencing the cost-effectiveness was the progression of HGAIN to anal cancer. At an annual transition probability below 0.001, the ICER was below $50,000. Vaccinating HIV-negative MSM treated for HGAIN decreases the lifetime risk of anal cancer and is likely to be a cost-effective intervention.
我们研究了四价人乳头瘤病毒(qHPV)疫苗作为二级/辅助预防策略,在预防27岁及以上HIV阴性男男性行为者(MSM)复发性高级别上皮内瘤变(HGAIN)方面的长期临床和经济效益。我们构建了一个马尔可夫模型,以评估两种策略的临床有效性和成本效益:(1)HGAIN治疗后不接种qHPV疫苗与(2)HGAIN治疗后接种qHPV疫苗。模型参数,包括肛管癌的自然史、以风险比(HR)衡量的疫苗效力(复发性HGAIN风险的降低)、HGAIN治疗效力、效用和成本,均从文献中获取。结果通过肛管癌的终生风险、终生成本、质量调整生命年和增量成本效益比(ICER)来衡量。对所有模型参数进行了敏感性分析。我们发现,对HIV阴性MSM进行疫苗接种可将肛管癌的终生风险降低60.77%,每质量调整生命年的ICER为87,240美元。结果对疫苗效力、HGAIN向肛管癌的转变、HGAIN治疗成本、疫苗随时间的保护程度以及疫苗保护持续时间高度敏感,而对HPV清除率、qHPV疫苗成本以及从正常到低级别肛管上皮内瘤变(LGAIN)和从正常到HGAIN的转变较不敏感。当HR为0.3时,ICER远低于50,000美元的支付意愿阈值;当HR为0.5时,ICER仍低于100,000美元的阈值。影响成本效益的最关键疾病相关因素是HGAIN向肛管癌的进展。当年度转变概率低于0.001时,ICER低于50,000美元。对接受HGAIN治疗的HIV阴性MSM进行疫苗接种可降低肛管癌的终生风险,并且可能是一种具有成本效益的干预措施。