Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Medicine, Weill Cornell Medical College, New York, NY, USA.
Blood Cancer J. 2018 Jun 12;8(6):60. doi: 10.1038/s41408-018-0089-0.
We sought to define the genomic landscape of diffuse large B-cell lymphoma (DLBCL) by using formalin-fixed paraffin-embedded (FFPE) biopsy specimens. We used targeted sequencing of genes altered in hematologic malignancies, including DNA coding sequence for 405 genes, noncoding sequence for 31 genes, and RNA coding sequence for 265 genes (FoundationOne-Heme). Short variants, rearrangements, and copy number alterations were determined. We studied 198 samples (114 de novo, 58 previously treated, and 26 large-cell transformation from follicular lymphoma). Median number of GAs per case was 6, with 97% of patients harboring at least one alteration. Recurrent GAs were detected in genes with established roles in DLBCL pathogenesis (e.g. MYD88, CREBBP, CD79B, EZH2), as well as notable differences compared to prior studies such as inactivating mutations in TET2 (5%). Less common GAs identified potential targets for approved or investigational therapies, including BRAF, CD274 (PD-L1), IDH2, and JAK1/2. TP53 mutations were more frequently observed in relapsed/refractory DLBCL, and predicted for lack of response to first-line chemotherapy, identifying a subset of patients that could be prioritized for novel therapies. Overall, 90% (n = 169) of the patients harbored a GA which could be explored for therapeutic intervention, with 54% (n = 107) harboring more than one putative target.
我们试图通过使用福尔马林固定石蜡包埋(FFPE)活检标本来定义弥漫性大 B 细胞淋巴瘤(DLBCL)的基因组景观。我们使用针对血液恶性肿瘤中改变的基因进行靶向测序,包括 405 个基因的 DNA 编码序列、31 个非编码序列和 265 个基因的 RNA 编码序列(FoundationOne-Heme)。确定了短变体、重排和拷贝数改变。我们研究了 198 个样本(114 个初治、58 个既往治疗和 26 个滤泡性淋巴瘤的大细胞转化)。每个病例的 GA 中位数为 6,97%的患者至少存在一种改变。在 DLBCL 发病机制中具有既定作用的基因中检测到了复发性 GA(例如 MYD88、CREBBP、CD79B、EZH2),与之前的研究相比也存在显著差异,例如 TET2 的失活突变(5%)。不太常见的 GA 确定了潜在的治疗靶点,包括 BRAF、CD274(PD-L1)、IDH2 和 JAK1/2。TP53 突变在复发/难治性 DLBCL 中更为常见,并且预测对一线化疗无反应,这确定了可以优先考虑新型疗法的患者子集。总体而言,90%(n=169)的患者存在可用于治疗干预的 GA,其中 54%(n=107)存在不止一个潜在靶点。