J Natl Cancer Inst. 2000 Mar 1;92(5):397-402. doi: 10.1093/jnci/92.5.397.
Human papillomavirus (HPV) infections appear to be central to the development of cervical cancer. This study addresses the question of whether testing women who have low-grade squamous intraepithelial lesions (LSILs) of the uterine cervix for HPV DNA is useful as a triage strategy.
Four clinical centers in different areas of the United States participated in a randomized clinical trial of the use of HPV DNA testing in women with cytologic evidence of atypical squamous cells of undetermined significance (ASCUS) or LSIL. The study sample in this article consists only of women who had LSIL at enrollment. Within 6 months of an LSIL diagnosis (based on a Pap smear read by a community-based cytopathologist), women who were 18 years of age or older completed a standardized questionnaire and underwent a pelvic examination that included collection of cervical specimens for HPV DNA testing by Hybrid Capture II (HCII)(R) assay.
Among the 642 women referred with LSIL who had analyzable test results, the mean chronologic age and age at first coitus were similar among the four clinical centers, despite the centers' ethnic and geographic diversity. Overall, HPV DNA was detected in cervical samples from 532 (82.9%) of the 642 women (95% confidence interval = 79.7%-85.7%). This high frequency of HPV positivity was confirmed by polymerase chain reaction (PCR) assays in a subset of 210 paired specimens tested by HCII and PCR (81.4% were positive by both methods).
Because a very high percentage of women with an LSIL diagnosis from Pap smears are positive for HPV DNA by HCII testing, there is limited potential for this assay to direct decisions about the clinical management of women with LSIL. The role of HPV testing in the management of women with ASCUS is still under study.
人乳头瘤病毒(HPV)感染似乎是宫颈癌发生的核心因素。本研究探讨了对患有子宫颈低度鳞状上皮内病变(LSIL)的女性进行HPV DNA检测作为一种分流策略是否有用的问题。
美国不同地区的四个临床中心参与了一项随机临床试验,该试验针对有意义不明确的非典型鳞状细胞(ASCUS)或LSIL细胞学证据的女性使用HPV DNA检测。本文中的研究样本仅包括入组时患有LSIL的女性。在LSIL诊断(基于社区细胞病理学家解读的巴氏涂片)后的6个月内,18岁及以上的女性完成一份标准化问卷,并接受盆腔检查,包括通过杂交捕获II(HCII)检测收集宫颈标本进行HPV DNA检测。
在642例转诊的LSIL女性中,有可分析检测结果的患者中,尽管四个临床中心在种族和地理上存在差异,但平均年龄和首次性交年龄相似。总体而言,642例女性中有532例(82.9%)的宫颈样本检测到HPV DNA(95%置信区间 = 79.7% - 85.7%)。在通过HCII和聚合酶链反应(PCR)检测的210对配对样本子集中,两种方法均证实了这种高HPV阳性率(81.4%两种方法均为阳性)。
由于通过巴氏涂片诊断为LSIL的女性中,HCII检测HPV DNA呈阳性的比例非常高,因此该检测对指导LSIL女性临床管理决策的潜力有限。HPV检测在ASCUS女性管理中的作用仍在研究中。