Kim Young-Gon, Ha Changhee, Jang Ja-Hyun, Jang Mi-Ae, Kim Jong-Won
Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Department of Laboratory Medicine, Konkuk University Medical Center, Konkuk University School of Medicine, Seoul, Republic of Korea.
Eur J Hum Genet. 2025 Jul 23. doi: 10.1038/s41431-025-01911-z.
Recently, new clinical genome resource (ClinGen) guidance focusing on cosegregation (PP1) and phenotype-specificity criteria (PP4) were introduced, based on the observation that the phenotype specificity could provide greater level of pathogenicity evidence. This study aimed to reassess variants of uncertain significance (VUS) found in tumor suppressor genes with specific phenotypes using these new recommendations. We retrieved VUS from an in-house database of all germline variants detected using sequencing since 2008. Patients carrying VUS from seven target tumor suppressor genes, NF1, TSC1, TSC2, RB1, PTCH1, STK11, and FH, were selected and the pathogenicity of each variant was reassessed using the new ClinGen PP1/PP4 criteria. In total, 128 unique VUS from 145 carriers were evaluated. Initial classification using the classic PP1/PP4 criteria from ACMG/AMP and point-based classification resulted in 21 variants being reclassified (2 pathogenic variants, 3 likely pathogenic variants [LPVs], 15 likely benign variants, and 1 benign variant), leaving 101 VUS. Applying the new ClinGen PP1/PP4 criteria, 32 (31.4%) remaining VUS were reclassified as LPVs. The reclassification rate was highest in STK11 (88.9%). Representative cases highlighted successful reclassification owing to highly specific phenotypes aligned with the new criteria. The new ClinGen PP1/PP4 criteria significantly improved the reclassification of VUS in tumor suppressor genes associated with specific phenotypes. The new criteria could substantially enhance the accuracy of variant classification.
最近,基于表型特异性可提供更高水平的致病性证据这一观察结果,引入了侧重于共分离(PP1)和表型特异性标准(PP4)的新临床基因组资源(ClinGen)指南。本研究旨在使用这些新建议重新评估在具有特定表型的肿瘤抑制基因中发现的意义未明变异(VUS)。我们从自2008年以来使用测序检测到的所有种系变异的内部数据库中检索VUS。选择携带来自7个目标肿瘤抑制基因(NF1、TSC1、TSC2、RB1、PTCH1、STK11和FH)的VUS的患者,并使用新的ClinGen PP1/PP4标准重新评估每个变异的致病性。总共评估了来自145名携带者的128个独特VUS。使用来自ACMG/AMP的经典PP1/PP4标准和基于点的分类进行初始分类,结果有21个变异被重新分类(2个致病性变异、3个可能致病性变异[LPV]、15个可能良性变异和1个良性变异),剩下101个VUS。应用新的ClinGen PP1/PP4标准,32个(31.4%)剩余的VUS被重新分类为LPV。STK11的重新分类率最高(88.9%)。代表性病例突出了由于与新标准一致的高度特异性表型而成功进行的重新分类。新的ClinGen PP1/PP4标准显著改善了与特定表型相关的肿瘤抑制基因中VUS的重新分类。新标准可大幅提高变异分类的准确性。