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宫颈癌筛查中HPV阳性女性的分流

Triage of HPV positive women in cervical cancer screening.

作者信息

Wentzensen Nicolas, Schiffman Mark, Palmer Timothy, Arbyn Marc

机构信息

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD, USA.

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD, USA.

出版信息

J Clin Virol. 2016 Mar;76 Suppl 1(Suppl 1):S49-S55. doi: 10.1016/j.jcv.2015.11.015. Epub 2015 Nov 28.

Abstract

Despite HPV vaccines, screening will remain central for decades to control cervical cancer. Recently, HPV testing alone or with cytology was introduced as an alternative to cytology screening. However, most HPV infections are harmless and additional tests are required to identify women with progressing infections or precancer. With three options for primary screening, and without clear strategies for triage of screen-positive women, there is great confusion about the best approach. Also, increasing HPV vaccination coverage will lead to lower disease prevalence, and force new screening approaches. Currently recommended triage strategies for primary HPV screening include HPV genotyping for HPV16 and HPV18 and cytology. Other alternatives that are currently evaluated include p16/Ki-67 dual stain cytology, host methylation, and viral methylation testing. Clinical management of women with cervical cancer screening results is moving to use risk thresholds rather than individual test results. Specific risk thresholds have been defined for return to primary screening, repeat testing, referral to colposcopy, and immediate treatment. Choice of test algorithms is based on comparison of absolute risk estimates from triage tests with established clinical thresholds. Importantly, triage tests need to be evaluated together with the primary screening test and the downstream clinical management. An optimal integrated screening and triage strategy should reassure the vast majority of women that they are at very low risk of cervical cancer, send the women at highest risk to colposcopy at the right time, when disease can be colposcopically detected, and minimize the intermediate risk group that requires continued surveillance.

摘要

尽管有HPV疫苗,但在未来几十年里,筛查仍将是控制宫颈癌的核心手段。最近,单独进行HPV检测或联合细胞学检查被引入作为细胞学筛查的替代方法。然而,大多数HPV感染是无害的,需要额外的检测来识别感染进展或癌前病变的女性。由于有三种初级筛查选项,且对于筛查阳性女性的分流没有明确策略,因此对于最佳方法存在很大困惑。此外,HPV疫苗接种覆盖率的提高将导致疾病患病率降低,并促使采用新的筛查方法。目前推荐的初级HPV筛查分流策略包括对HPV16和HPV18进行HPV基因分型以及细胞学检查。目前正在评估的其他替代方法包括p16/Ki-67双重染色细胞学检查、宿主甲基化检测和病毒甲基化检测。宫颈癌筛查结果的临床管理正朝着使用风险阈值而非个体检测结果的方向发展。已为重新进行初级筛查、重复检测、转诊至阴道镜检查和立即治疗定义了特定的风险阈值。检测算法的选择基于将分流检测的绝对风险估计值与既定临床阈值进行比较。重要的是,分流检测需要与初级筛查检测及下游临床管理一起进行评估。一种最佳的综合筛查和分流策略应让绝大多数女性放心,她们患宫颈癌的风险非常低,在疾病可通过阴道镜检测到时,将风险最高的女性及时转诊至阴道镜检查,并尽量减少需要持续监测的中间风险组。

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