Department of Pathology, VU University Medical Center, De Boelelaan 1117, 1081 HV Amsterdam, The Netherlands.
Department of Obstetrics and Gynaecology, Radboud University Medical Center, PO Box 9101, 6500 HB Nijmegen, The Netherlands.
Gynecol Oncol. 2014 Oct;135(1):58-63. doi: 10.1016/j.ygyno.2014.08.003. Epub 2014 Aug 8.
Methylation marker analysis using bi-marker panel MAL/miR-124-2 is a promising triage test for identifying cervical (pre)cancer in high-risk human papillomavirus (hrHPV) positive women. Bi-marker panel MAL/miR-124-2 can be applied directly on self-sampled cervico-vaginal material and its sensitivity is non-inferior to that of cytology, yet at the cost of more colposcopy referrals. Our objective was to increase specificity of MAL/miR-124-2 methylation analysis by varying the assay thresholds and adding HPV16/18 genotyping.
1019 hrHPV-positive women were selected from a randomized controlled self-sampling trial (PROHTECT-3; 33-63 years, n=46,001) and nine triage strategies with methylation testing of MAL/miR-124-2 and HPV16/18 genotyping were evaluated. The methylation assay threshold was set at four different predefined levels which correspond with clinical specificities for end-point cervical intra-epithelial grade 3 or worse (CIN3+) of 50%, 60%, 70%, and 80%.
The CIN3+ sensitivity of methylation analysis decreased (73.5 to 44.9%) while specificity increased (47.2 to 83.4%) when increasing the assay threshold. CIN3+ sensitivity and specificity of HPV16/18 genotyping were 68.0% and 65.6%, respectively. Combined methylation analysis at threshold-80 and HPV16/18 genotyping yielded similar CIN3+ sensitivity as that of methylation only at threshold-50 (77.6%) with an increased specificity (54.8%).
Combined triage by MAL/miR-124-2 methylation analysis with threshold-80 and HPV16/18 genotyping reaches high CIN3+ sensitivity with increased specificity to identify women with cervical (pre)cancer among HPV self-sample positive women. The combined strategy is attractive as it is fully molecular and identifies women at the highest risk of cervical (pre)cancer because of strongly elevated methylation levels and/or HPV16/18 positivity.
使用双标志物面板 MAL/miR-124-2 进行甲基化标记分析是一种很有前途的用于识别高危型人乳头瘤病毒(hrHPV)阳性女性宫颈癌(前)癌的分流测试。双标志物面板 MAL/miR-124-2 可直接应用于自采样的宫颈阴道材料,其敏感性不低于细胞学,但需要更多的阴道镜转诊。我们的目的是通过改变检测阈值并增加 HPV16/18 基因分型来提高 MAL/miR-124-2 甲基化分析的特异性。
从一项随机对照自我采样试验(PROHTECT-3;33-63 岁,n=46001)中选择了 1019 名 hrHPV 阳性女性,并评估了 9 种基于 MAL/miR-124-2 和 HPV16/18 基因分型的分流策略。甲基化检测的检测阈值设定为四个不同的预设水平,分别对应终点宫颈上皮内瘤变 3 级或更高级别(CIN3+)的临床特异性为 50%、60%、70%和 80%。
随着检测阈值的增加,甲基化分析的 CIN3+敏感性(73.5%降至 44.9%)降低,特异性(47.2%升至 83.4%)增加。HPV16/18 基因分型的 CIN3+敏感性和特异性分别为 68.0%和 65.6%。阈值-80 时的 MAL/miR-124-2 甲基化分析与 HPV16/18 基因分型联合检测的 CIN3+敏感性与仅阈值-50 时的 MAL/miR-124-2 甲基化分析相似(77.6%),特异性增加(54.8%)。
MAL/miR-124-2 甲基化分析联合阈值-80 与 HPV16/18 基因分型的联合分流达到了较高的 CIN3+敏感性,并提高了特异性,以识别 HPV 自我采样阳性女性中的宫颈癌(前)癌患者。由于高度升高的甲基化水平和/或 HPV16/18 阳性,该联合策略很有吸引力,因为它是完全分子的,可以识别宫颈癌(前)癌风险最高的女性。