Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Department of Clinical Genetics and Pathology, Division of Laboratory Medicine, Lund, Sweden.
Lab Invest. 2022 Aug;102(8):838-845. doi: 10.1038/s41374-022-00770-2. Epub 2022 Mar 22.
Morphologic and immunohistochemical analysis of preoperative core needle biopsies (CNB) is important in the management of patients with soft tissue and bone tumors (STBTs). Most SBTB subtypes have more or less extensive DNA copy number aberrations (CNA), potentially providing useful diagnostic information. To evaluate the technical feasibility of single nucleotide polymorphism (SNP) array analysis and the diagnostic usefulness of the copy number profiles, we studied CNBs from 171 patients with suspected STBTs. SNP array analysis could be performed on 168 (98%) of the samples. The CNA profile was compatible with the CNB diagnosis in 87% of the cases. Discrepant cases were dominated by false-negative results due to nonrepresentative material or contamination with normal cells. 70 genomic profiles were indicative of specific histopathologic tumor entities and in agreement with the corresponding CNB diagnoses in 83%. In 96 of the cases with aberrant CNA profiles, the SNP profiles were of sufficient quality for segmentation, allowing clustering analysis on the basis of the Jaccard similarity index. The analysis of these segment files showed three major CNA clusters, based on the complexity levels and the predominance of gains versus losses. For 43 of these CNB samples, we had SNP array data also from their corresponding surgical samples. In 33 of these pairs, the two corresponding samples clustered next to each other, with Jaccard scores ranging from 0.61 to 0.99 (median 0.96). Also, for those tumor pairs that did not cluster together, the Jaccard scores were relatively high (median 0.9). 10 cases showed discrepant results, mainly due to varying degrees of normal cell contamination or technical issues. Thus, the copy number profile seen in a CNB is typically highly representative of the major cell population in the tumor.
术前核心针活检 (CNB) 的形态学和免疫组织化学分析对于软组织和骨肿瘤 (STBT) 患者的管理非常重要。大多数 SBTB 亚型或多或少具有广泛的 DNA 拷贝数异常 (CNA),这可能提供了有用的诊断信息。为了评估单核苷酸多态性 (SNP) 阵列分析的技术可行性和拷贝数谱的诊断有用性,我们研究了 171 例疑似 STBT 患者的 CNB。SNP 阵列分析可在 168 例(98%)样本上进行。在 87%的病例中,CNA 谱与 CNB 诊断相吻合。不一致的病例主要是由于代表性材料不足或正常细胞污染导致的假阴性结果。70 个基因组谱提示了特定的组织病理学肿瘤实体,并与相应的 CNB 诊断一致,占 83%。在 96 例 CNA 谱异常的病例中,SNP 谱的质量足以进行分割,允许基于 Jaccard 相似指数进行聚类分析。这些片段文件的分析显示,基于复杂性水平和增益与缺失的优势,存在三个主要的 CNA 簇。对于其中的 43 例 CNB 样本,我们还从其相应的手术样本中获得了 SNP 阵列数据。在这 33 对样本中,两个相应的样本彼此相邻聚类,Jaccard 得分范围为 0.61 至 0.99(中位数 0.96)。此外,对于那些没有聚类在一起的肿瘤对,Jaccard 得分相对较高(中位数 0.9)。10 例显示不一致的结果,主要是由于不同程度的正常细胞污染或技术问题。因此,CNB 中看到的拷贝数谱通常高度代表肿瘤中主要细胞群体。