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利用新型肿瘤特异性测序 panel 检测福尔马林固定石蜡包埋肿瘤样本中的双等位基因 DNA 修复基因缺失。

Detection of Biallelic Loss of DNA Repair Genes in Formalin-Fixed, Paraffin-Embedded Tumor Samples Using a Novel Tumor-Only Sequencing Panel.

机构信息

Repare Therapeutics, Cambridge, Massachusetts.

Memorial Sloan Kettering Cancer Center, New York, New York.

出版信息

J Mol Diagn. 2023 May;25(5):295-310. doi: 10.1016/j.jmoldx.2023.02.004. Epub 2023 Mar 20.

DOI:10.1016/j.jmoldx.2023.02.004
PMID:36944408
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10340082/
Abstract

Patient selection for synthetic lethal-based cancer therapy may be improved by assessment of gene-specific loss of heterozygosity (LOH) and biallelic loss of function (LOF). This report describes SyNthetic lethal Interactions for Precision Diagnostics (SNiPDx), a targeted next-generation sequencing (NGS) panel for detection of LOH and biallelic LOF alterations in 26 target genes focused on DNA damage response pathways, in tumor-only formalin-fixed, paraffin-embedded (FFPE) samples. NGS was performed across all exons of these 26 genes and encompassed a total of 7632 genome-wide single-nucleotide polymorphisms on genomic DNA from 80 FFPE solid tumor samples. The Fraction and Allele-Specific Copy Number Estimates from Tumor Sequencing algorithm was optimized to assess tumor purity and copy number based on heterozygous single-nucleotide polymorphisms. SNiPDx demonstrated high sensitivity (95%) and specificity (91%) for LOH detection compared with whole genome sequencing. Positive agreement with local NGS-based testing in the detection of genetic alterations was 95%. SNiPDx detected 93% of biallelic ATM LOF mutations, 100% of ATM single-nucleotide variants and small insertions/deletions, and 100% of all ATM LOH status events identified by orthogonal NGS-based testing. SNiPDx is a novel, clinically feasible test for analysis of allelic status in FFPE tumor samples, which demonstrated high accuracy when compared with other NGS-based approaches in clinical use.

摘要

基于合成致死的癌症治疗的患者选择可以通过评估基因特异性杂合性丢失 (LOH) 和双等位基因功能丧失 (LOF) 来改善。本报告描述了基于合成致死相互作用的精准诊断 (SNiPDx),这是一种针对 DNA 损伤反应途径中 26 个靶基因的靶向下一代测序 (NGS) 面板,用于检测肿瘤中仅有的福尔马林固定石蜡包埋 (FFPE) 样本中的 LOH 和双等位基因 LOF 改变。NGS 在这些 26 个基因的所有外显子上进行,总共涵盖了来自 80 个 FFPE 固体肿瘤样本基因组 DNA 中的 7632 个全基因组单核苷酸多态性。肿瘤测序算法的分数和等位基因特异性拷贝数估计被优化,以基于杂合单核苷酸多态性评估肿瘤纯度和拷贝数。与全基因组测序相比,SNiPDx 检测 LOH 的灵敏度 (95%) 和特异性 (91%) 均较高。在检测遗传改变方面,与本地基于 NGS 的检测具有 95% 的阳性一致性。SNiPDx 检测到 93% 的双等位基因 ATM LOF 突变、100% 的 ATM 单核苷酸变异和小插入/缺失,以及所有通过正交基于 NGS 的检测确定的 ATM LOH 状态事件的 100%。SNiPDx 是一种新颖的、临床上可行的用于分析 FFPE 肿瘤样本等位基因状态的测试方法,与临床使用的其他基于 NGS 的方法相比,其准确性较高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ff8/10340082/71a8d08ce2db/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ff8/10340082/74b11b9c00bd/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ff8/10340082/fc5b4b9e7d7c/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ff8/10340082/0470705604f9/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ff8/10340082/6a7466520660/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ff8/10340082/bc0009c67350/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ff8/10340082/71a8d08ce2db/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ff8/10340082/74b11b9c00bd/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ff8/10340082/fc5b4b9e7d7c/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ff8/10340082/0470705604f9/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ff8/10340082/6a7466520660/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ff8/10340082/bc0009c67350/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ff8/10340082/71a8d08ce2db/gr6.jpg

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