Liman Agnes K, Giampoli Ellen J, Bonfiglio Thomas A
Department of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, New York 14642, USA.
Cancer. 2005 Dec 25;105(6):457-60. doi: 10.1002/cncr.21387.
The 2001 American Society for Colposcopy and Cervical Pathology Consensus Guidelines recommend that women who have Papanicolaou (Pap) smears diagnosed as atypical squamous cells (ASC), cannot exclude high-grade squamous intraepithelial lesion (HSIL) (ASC-H) should be referred for immediate colposcopic examination. The objective of this pilot study was to evaluate whether reflex human papillomavirus (HPV)-DNA testing performed on smears diagnosed as ASC-H may obviate the need for immediate colposcopic examination.
All ThinPrep Pap smears that were diagnosed as ASC-H or atypical squamous metaplastic cells (ASMT) between 2001-2003 and that had HPV-DNA testing and subsequent histologic and/or cytologic follow-up were evaluated. Those smears that were diagnosed as ASMT were reviewed and reclassified under the 2001 Bethesda System as either ASC of undetermined significance (ASCUS) or ASC-H. Smears that were diagnosed as ASCUS were excluded from the study.
The study included of 48 smears that were diagnosed as ASC-H. All patients with biopsy-proven HSIL had positive high-risk (HR)-HPV results (100% negative predictive value). Approximately 80% of patients with ASC-H who had biopsy-proven, low-grade intraepithelial lesion on follow-up had positive HR-HPV results. Among the patients who had ASC-H with negative follow-up, 50% had positive HR-HPV results, and 50% had negative HR-HPV results.
Among patients with ASC-H, a negative HR-HPV result was found to be an excellent predictor of the absence of HSIL. The results of this pilot study suggested that HPV-DNA testing may serve as a means to better select which patients with ASC-H on Pap smear should undergo colposcopic examination. This approach potentially may reduce medical costs and eliminate the need for routine colposcopic examination among patients with ASC-H Pap smears.
2001年美国阴道镜和宫颈病理学会共识指南建议,巴氏涂片诊断为非典型鳞状细胞(ASC)、不能排除高级别鳞状上皮内病变(HSIL)(ASC-H)的女性应立即转诊进行阴道镜检查。这项初步研究的目的是评估对诊断为ASC-H的涂片进行人乳头瘤病毒(HPV)-DNA检测是否可以避免立即进行阴道镜检查。
对2001年至2003年间诊断为ASC-H或非典型鳞状化生细胞(ASMT)且进行了HPV-DNA检测以及随后的组织学和/或细胞学随访的所有薄层液基巴氏涂片进行评估。对诊断为ASMT的涂片进行复查,并根据2001年贝塞斯达系统重新分类为意义不明确的ASC(ASCUS)或ASC-H。诊断为ASCUS的涂片被排除在研究之外。
该研究包括48例诊断为ASC-H的涂片。所有经活检证实为HSIL的患者高危(HR)-HPV检测结果均为阳性(阴性预测值为100%)。随访中经活检证实为低级别上皮内病变的ASC-H患者中,约80%的HR-HPV检测结果为阳性。在随访结果为阴性的ASC-H患者中,50%的HR-HPV检测结果为阳性,50%为阴性。
在ASC-H患者中,HR-HPV检测结果为阴性是不存在HSIL的极佳预测指标。这项初步研究的结果表明,HPV-DNA检测可作为一种手段,更好地选择巴氏涂片为ASC-H的哪些患者应接受阴道镜检查。这种方法有可能降低医疗成本,并消除ASC-H巴氏涂片患者进行常规阴道镜检查的必要性。