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The Clinical and Economic Benefits of Co-Testing Versus Primary HPV Testing for Cervical Cancer Screening: A Modeling Analysis

机译:宫颈癌筛查的共同检测与主要HPV检测的临床和经济效益:模型分析

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Background: Consensus United States cervical cancer screening guidelines recommend use of combination Pap plus human papillomavirus (HPV) testing for women aged 30 to 65 years. An HPV test was approved by the Food and Drug Administration in 2014 for primary cervical cancer screening in women age 25 years and older. Here, we present the results of clinical-economic comparisons of Pap plus HPV mRNA testing including genotyping for HPV 16/18 (co-testing) versus DNA-based primary HPV testing with HPV 16/18 genotyping and reflex cytology (HPV primary) for cervical cancer screening.
机译:背景:共识性美国宫颈癌筛查指南建议针对30至65岁的女性使用联合Pap联合人乳头瘤病毒(HPV)检测。 2014年,美国食品药品监督管理局(FDA)批准了一项HPV测试,以筛查25岁以上女性的原发性宫颈癌。在这里,我们介绍了Pap和HPV mRNA测试的临床经济比较结果,包括HPV 16/18的基因分型(共同测试)与HPV 16/18基因型和反射细胞学(基于HPV的原代)的基于DNA的主要HPV测试宫颈癌筛查。

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