Jolien de Waard , Arkajyoti Bhattacharya , Martine T. de Boer , Bettien M. van Hemel , Martha D. Esajas , Karin M. Vermeulen , Geertruida H. de Bock , Ed Schuuring , G. Bea A. Wisman
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In this study, we determined the sensitivity and specificity of 2 commercial assays using quantitative methylation-specific PCR. DNA from the same cohort of high-risk human papillomavirus-positive self-sampled material obtained through the population-based screening program in the North of the Netherlands from women with CIN2 or less (<CIN3, n = 208) and women with CIN3+ (n = 96) was used. The QIAsure methylation test (consisting of 2 methylation markers) showed a sensitivity of 65% and a specificity of 72%, whereas the Gyntect assay (consisting of 6 methylation markers) showed a sensitivity of 59% and a specificity of 91% for CIN3+. When we compared all individual 23 methylation markers, receiver operating characteristic analysis showed an area under the curve of ≥0.7 for 11 of 23 markers (<em>P</em> < .001). By model-based recursive partitioning and robustness analysis, we found a panel with a better sensitivity compared with QIAsure and Gyntect (<em>P</em> < .001). This new panel, consisting of <em>ITGA4</em>, <em>ASCL1</em>, and <em>FAM19A4,</em> has a sensitivity of 84% and a specificity of 70%, similar to our previously identified panel (<em>ANKRD18CP</em>, <em>LHX8</em>, and <em>EPB41L3</em>). Thus, in addition to our previously identified panel, the combination of <em>ITGA4</em>, <em>ASCL1</em>, and <em>FAM19A4</em> showed good diagnostic performance and potentially can replace cytology, thereby avoiding additional doctor visits for many women worldwide and reducing the time for decision making for referral to the gynecologist.</p></div>","PeriodicalId":18706,"journal":{"name":"Modern Pathology","volume":"37 8","pages":"Article 100528"},"PeriodicalIF":7.1000,"publicationDate":"2024-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S089339522400108X/pdfft?md5=7f039bde8c816265f35e7c8861ad19d9&pid=1-s2.0-S089339522400108X-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Methylation Analysis to Detect CIN3+ in High-Risk Human Papillomavirus-Positive Self-Samples From the Population-Based Cervical Cancer Screening Program\",\"authors\":\"Jolien de Waard , Arkajyoti Bhattacharya , Martine T. de Boer , Bettien M. van Hemel , Martha D. 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引用次数: 0
摘要
自 2017 年起,荷兰基于人群的筛查计划(PBS)引入了自采样装置,以提高参与率。然而,常规分流细胞学检查无法在自采样材料上进行。甲基化是一种替代分流方法,可直接在自取样本中提取的 DNA 上进行。最近,我们测试了一组 15 个已发表的宫颈上皮内瘤变 3 级或更差(CIN3+)特异性甲基化标记物,发现其中三个标记物的灵敏度为 82%,特异性为 74%。在本研究中,我们使用定量甲基化特异性 PCR(QMSP)测定了两种商业检测方法的灵敏度和特异性。从荷兰北部 CIN2 或 CIN2 以下妇女通过 PBS 采集的高危人乳头状瘤病毒(hrHPV)阳性自采样材料中提取的 DNA (
Methylation Analysis to Detect CIN3+ in High-Risk Human Papillomavirus-Positive Self-Samples From the Population-Based Cervical Cancer Screening Program
Since 2017, a self-sampling device has been introduced to the Dutch population-based screening program to enable higher participation rates. However, routine triage cytology cannot be performed on self-sampling material. Methylation is an alternative triage method that can be performed directly on DNA extracted from self-samples. Recently, we tested a set of 15 published cervical intraepithelial neoplasia grade 3 or worse (CIN3+)-specific methylation markers and found a panel of 3 markers with a sensitivity of 82% and a specificity of 74%. In this study, we determined the sensitivity and specificity of 2 commercial assays using quantitative methylation-specific PCR. DNA from the same cohort of high-risk human papillomavirus-positive self-sampled material obtained through the population-based screening program in the North of the Netherlands from women with CIN2 or less (<CIN3, n = 208) and women with CIN3+ (n = 96) was used. The QIAsure methylation test (consisting of 2 methylation markers) showed a sensitivity of 65% and a specificity of 72%, whereas the Gyntect assay (consisting of 6 methylation markers) showed a sensitivity of 59% and a specificity of 91% for CIN3+. When we compared all individual 23 methylation markers, receiver operating characteristic analysis showed an area under the curve of ≥0.7 for 11 of 23 markers (P < .001). By model-based recursive partitioning and robustness analysis, we found a panel with a better sensitivity compared with QIAsure and Gyntect (P < .001). This new panel, consisting of ITGA4, ASCL1, and FAM19A4, has a sensitivity of 84% and a specificity of 70%, similar to our previously identified panel (ANKRD18CP, LHX8, and EPB41L3). Thus, in addition to our previously identified panel, the combination of ITGA4, ASCL1, and FAM19A4 showed good diagnostic performance and potentially can replace cytology, thereby avoiding additional doctor visits for many women worldwide and reducing the time for decision making for referral to the gynecologist.
期刊介绍:
Modern Pathology, an international journal under the ownership of The United States & Canadian Academy of Pathology (USCAP), serves as an authoritative platform for publishing top-tier clinical and translational research studies in pathology.
Original manuscripts are the primary focus of Modern Pathology, complemented by impactful editorials, reviews, and practice guidelines covering all facets of precision diagnostics in human pathology. The journal's scope includes advancements in molecular diagnostics and genomic classifications of diseases, breakthroughs in immune-oncology, computational science, applied bioinformatics, and digital pathology.