Clinical significance of extended high-risk human papillomavirus genotyping and viral load in cervical cancer and precancerous lesions

Q4 Medicine
Pingping Su , Jincheng Ma , Lirui Yu , Shuting Tang , Pengming Sun
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引用次数: 1

Abstract

Persistent infections with specific high-risk human papillomavirus (HR-HPV) strains are the leading cause of cervical cancer and precancerous lesions. HPV-16 and HPV-18 are associated with more than 70% of cervical cancer. However, with recent widespread vaccination efforts against cervical cancer, the infection rates of HPV-16 and HPV-18 have decreased across all age groups, while the infection rates of other HR-HPV strains have increased. The non-16/18 HR-HPV strains play an important role in cervical lesions. These strains can be identified with extended genotyping, and the 2019 American Society for Colposcopy and Cervical Pathology (ASCCP) guidelines recommended an HPV-based testing to assess the risk of cervical disease in patients. We reviewed and analyzed the clinical benefits of applying extended HR-HPV genotyping, which was published by the International Agency for Research on Cancer (HPV-16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68), to cervical cancer screening. This review concluded that cervical cancer screening needs to include extended HR-HPV genotyping. The examination of extended HR-HPV genotyping in cervical intraepithelial lesions and cervical cancers can help guide clinical practices.

高危人乳头瘤病毒基因分型及病毒载量在宫颈癌及癌前病变中的临床意义
特定高危人乳头瘤病毒(HR-HPV)株持续感染是宫颈癌和癌前病变的主要原因。HPV-16和HPV-18与超过70%的宫颈癌有关。然而,随着最近广泛开展宫颈癌疫苗接种工作,HPV-16和HPV-18的感染率在所有年龄组中都有所下降,而其他HR-HPV毒株的感染率有所上升。非16/18 HR-HPV株在宫颈病变中起重要作用。这些菌株可以通过扩展基因分型来识别,2019年美国阴道镜和宫颈病理学会(ASCCP)指南建议采用基于hpv的检测来评估患者宫颈疾病的风险。我们回顾并分析了国际癌症研究机构发布的扩展HR-HPV基因分型(HPV-16、18、31、33、35、39、45、51、52、56、58、59、66和68)应用于宫颈癌筛查的临床益处。这篇综述的结论是宫颈癌筛查需要包括扩展的HR-HPV基因分型。宫颈上皮内病变和宫颈癌的扩展HR-HPV基因分型检查可以帮助指导临床实践。
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来源期刊
Gynecology and Obstetrics Clinical Medicine
Gynecology and Obstetrics Clinical Medicine Medicine-Obstetrics and Gynecology
CiteScore
0.70
自引率
0.00%
发文量
35
审稿时长
18 weeks
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