Department of Gynecologic Oncology, Zeynep Kamil Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.
Department of Pathology, Zeynep Kamil Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.
Diagn Cytopathol. 2021 Feb;49(2):267-272. doi: 10.1002/dc.24633. Epub 2020 Oct 2.
We aimed to present the biopsy results of women with HPV 16/18 infection and investigate whether cytology is necessary as a part of routine cervical cancer screening in women with HPV 16/18.
This is a retrospective cohort study conducted on 1647 patients between the ages of 30 and 65 years with HPV 16/18 undergoing colposcopy-guided biopsy at a tertiary gynecological cancer center between January-2016 and January-2019. We compared the preinvasive lesion rates and the invasive cervical cancer rates of women with HPV 16/18 between the negative and the abnormal cytology group.
Of the 1647 women, 1105 (67.1%) had negative cytology and 542 (32.9%) had abnormal cytology. Among women with initial negative cytology, cervical intraepithelial neoplasia (CIN) 2+ lesion was detected in 205 (18.6%) women. The rate of CIN 2+ lesion in women with abnormal cytology was 28%. There was a significant difference between negative and abnormal cytology group in terms of CIN 2+ lesion rates (P < .001). Among women with initial negative cytology, invasive cervical cancer was detected in 6 (0.5%) women. The rate of invasive cervical cancer in women with abnormal cytology was 8 (1.5%). There was no significant difference between negative and abnormal cytology group in terms of invasive cervical cancer rates (P = .082).
The rate of cervical cancer among HPV 16/18-infected women with negative cytology is similar to women with abnormal cytology. Based on the results of this study, Pap testing could be unnecessary in HPV 16/18-infected women to diagnose invasive cervical cancer who will undergo colposcopy biopsy.
本研究旨在展示 HPV 16/18 感染女性的活检结果,并探讨在 HPV 16/18 感染女性中,细胞学检查是否有必要作为宫颈癌常规筛查的一部分。
这是一项回顾性队列研究,纳入了 2016 年 1 月至 2019 年 1 月期间在一家三级妇科癌症中心因 HPV 16/18 行阴道镜引导下活检的 1647 例年龄在 30 至 65 岁的患者。我们比较了 HPV 16/18 感染的女性中细胞学检查阴性组和细胞学检查异常组的宫颈上皮内瘤变(CIN)率和浸润性宫颈癌率。
1647 例女性中,1105 例(67.1%)细胞学检查阴性,542 例(32.9%)细胞学检查异常。在初始细胞学检查阴性的女性中,205 例(18.6%)发现 CIN 2+病变。细胞学检查异常组的 CIN 2+病变率为 28%。CIN 2+病变率在细胞学检查阴性组和异常组之间有显著差异(P<0.001)。在初始细胞学检查阴性的女性中,6 例(0.5%)发现浸润性宫颈癌。细胞学检查异常组的浸润性宫颈癌率为 8 例(1.5%)。两组间浸润性宫颈癌率无显著差异(P=0.082)。
HPV 16/18 感染女性中细胞学检查阴性者的宫颈癌发生率与细胞学检查异常者相似。基于本研究结果,HPV 16/18 感染行阴道镜活检的女性可能无需进行巴氏涂片检查来诊断浸润性宫颈癌。