Agency for Public Health Lazio Sanità, Rome, Italy.
PLoS One. 2013;8(2):e57600. doi: 10.1371/journal.pone.0057600. Epub 2013 Feb 27.
Pap test, and especially HPV DNA test, identify a large group of women who do not have any clinically relevant lesions, i.e., CIN2+ (Cervical Intraepithelial Neoplasia grade 2 or worse), but who are at greater risk of getting lesions in the future. The follow up of these women needs new biomarkers with prognostic value. The objective of this study is to evaluate the prognostic value of E6/E7 mRNA over-expression assay (PreTect HPV-Proofer, Norchip) for 5 HR-HPV types (16, 18, 31, 33, and 45) for progression to CIN2+ after a negative colposcopy. This prospective study, conducted at four Italian centres, enrolled 673 women with either a negative colposcopy or a negative or CIN1 histology. The clinical end-point was histological confirmation of CIN2+. Women were classified at baseline according to mRNA results and managed according to local colposcopy protocols. At least one conclusive follow-up test was obtained for 347 women (25 months average lapse since recruitment, range 5-74). Only seven CIN2+ were detected during follow up, three among the 82 women positive for mRNA at baseline, two among the 250 negative (Fisher exact test, p = 0.02), and two among the 12 with an invalid test. Absolute CIN2+ risk was 6.7/1,000 person/years in the whole cohort. The absolute CIN2+ risk was 18.4/1,000 person/years and 3.6/1,000 person/years in mRNA-positive and mRNA-negative women, respectively. In conclusion, E6/E7 mRNA over-expression appears to be a good candidate as a prognostic biomarker to manage HR-HPV DNA-positive women with negative colposcopy or histology, particularly in order to decrease follow-up intensity in those who are negative.
巴氏涂片检查,尤其是 HPV DNA 检测,可以识别出一大群没有任何临床相关病变的女性,即 CIN2+(宫颈上皮内瘤变 2 级或更高级别),但她们未来患病变的风险更高。这些女性的随访需要具有预后价值的新生物标志物。本研究旨在评估针对 5 种高危型 HPV(16、18、31、33 和 45)的 E6/E7mRNA 过表达检测(PreTect HPV-Proofer,Norchip)对阴性阴道镜检查后进展为 CIN2+的预测价值。这项前瞻性研究在意大利的四个中心进行,共纳入了 673 名女性,其阴道镜检查结果为阴性或组织学为阴性或 CIN1。主要终点为 CIN2+的组织学确认。根据 mRNA 结果对女性进行基线分类,并根据当地阴道镜检查方案进行管理。347 名女性至少获得了一次明确的随访检测(招募后平均随访时间为 25 个月,范围为 5-74 个月)。在随访期间仅发现 7 例 CIN2+,其中 3 例在基线时 mRNA 检测呈阳性,2 例在 250 例阴性患者中,2 例在 12 例无效检测患者中(Fisher 精确检验,p=0.02)。整个队列的绝对 CIN2+风险为 6.7/1000 人/年。mRNA 阳性和阴性女性的绝对 CIN2+风险分别为 18.4/1000 人/年和 3.6/1000 人/年。综上所述,E6/E7mRNA 过表达似乎是一种很好的预后生物标志物候选物,可用于管理 HPV DNA 阳性但阴道镜检查或组织学为阴性的女性,尤其是对于那些阴性的女性,有助于降低随访强度。