首页> 外文期刊>Journal of the National Cancer Institute >Cost-effectiveness of cervical cancer screening with human papillomavirus DNA testing and HPV-16,18 vaccination.
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Cost-effectiveness of cervical cancer screening with human papillomavirus DNA testing and HPV-16,18 vaccination.

机译:用人乳头瘤病毒DNA测试和HPV-16,18疫苗接种进行子宫颈癌筛查的成本效益。

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BACKGROUND: The availability of human papillomavirus (HPV) DNA testing and vaccination against HPV types 16 and 18 (HPV-16,18) motivates questions about the cost-effectiveness of cervical cancer prevention in the United States for unvaccinated older women and for girls eligible for vaccination. METHODS: An empirically calibrated model was used to assess the quality-adjusted life years (QALYs), lifetime costs, and incremental cost-effectiveness ratios (2004 US dollars per QALY) of screening, vaccination of preadolescent girls, and vaccination combined with screening. Screening varied by initiation age (18, 21, or 25 years), interval (every 1, 2, 3, or 5 years), and test (HPV DNA testing of cervical specimens or cytologic evaluation of cervical cells with a Pap test). Testing strategies included: 1) cytology followed by HPV DNA testing for equivocal cytologic results (cytology with HPV test triage); 2) HPV DNA testing followed by cytology for positive HPV DNA results (HPV test with cytology triage); and 3) combined HPV DNA testing and cytology. Strategies were permitted to switch once at age 25, 30, or 35 years. RESULTS: For unvaccinated women, triennial cytology with HPV test triage, beginning by age 21 years and switching to HPV testing with cytology triage at age 30 years, cost Dollars 78,000 per QALY compared with the next best strategy. For girls vaccinated before age 12 years, this same strategy, beginning at age 25 years and switching at age 35 years, cost Dollars 41,000 per QALY with screening every 5 years and Dollars 188,000 per QALY screening triennially, each compared with the next best strategy. These strategies were more effective and cost-effective than screening women of all ages with cytology alone or cytology with HPV triage annually or biennially. CONCLUSIONS: For both vaccinated and unvaccinated women, age-based screening by use of HPV DNA testing as a triage test for equivocal results in younger women and as a primary screening test in older women is expected to be more cost-effective than current screening recommendations.
机译:背景:人类乳头瘤病毒(HPV)DNA检测和针对16型和18型HPV(HPV-16,18)疫苗的可利用性引发了以下问题:在美国,未接种疫苗的老年妇女和符合条件的女孩子宫颈癌预防的成本效益进行疫苗接种。方法:使用经验校准模型评估筛查,青春期前女孩的疫苗接种以及疫苗接种与筛查的质量调整生命年(QALYs),终生成本和增量成本效益比(2004美元/ QALY)。筛选因起始年龄(18、21或25岁),间隔(每1、2、3或5年)和测试(宫颈标本的HPV DNA测试或通过Pap测试对宫颈细胞的细胞学评估)而异。检测策略包括:1)细胞学检查,然后进行HPV DNA检测以获取模棱两可的细胞学检查结果(使用HPV检测分类进行细胞学检查); 2)HPV DNA测试,然后进行细胞学检查,以得出阳性的HPV DNA结果(带有细胞学分类的HPV测试); 3)结合HPV DNA检测和细胞学检查。策略允许在25、30或35岁时切换一次。结果:对于未接种疫苗的女性,从21岁开始,每三年一次进行HPV测试分类的细胞学检查,然后在30岁时转为进行细胞学分类的HPV检测,与次优策略相比,每QALY花费7.8万美元。对于在12岁之前接种疫苗的女孩,从25岁开始到35岁时进行转换的相同策略,每QALY每5年进行一次筛查的费用为41,000美元,每QALY每三年进行一次筛查的费用为188,000美元,与次优策略相比。这些策略比每年或每两年对所有年龄的仅进行细胞学检查或通过HPV分流进行细胞学检查的妇女进行筛查更为有效和具有成本效益。结论:对于已接种疫苗的妇女和未接种疫苗的妇女,通过使用HPV DNA检测作为年龄较大的女性的模棱两可的分类检查和年龄较大的女性的初级筛查,按年龄进行的筛查比当前的筛查建议更具成本效益。 。

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