He Jie, Abdel-Wahab Omar, Nahas Michelle K, Wang Kai, Rampal Raajit K, Intlekofer Andrew M, Patel Jay, Krivstov Andrei, Frampton Garrett M, Young Lauren E, Zhong Shan, Bailey Mark, White Jared R, Roels Steven, Deffenbaugh Jason, Fichtenholtz Alex, Brennan Timothy, Rosenzweig Mark, Pelak Kimberly, Knapp Kristina M, Brennan Kristina W, Donahue Amy L, Young Geneva, Garcia Lazaro, Beckstrom Selmira T, Zhao Mandy, White Emily, Banning Vera, Buell Jamie, Iwanik Kiel, Ross Jeffrey S, Morosini Deborah, Younes Anas, Hanash Alan M, Paietta Elisabeth, Roberts Kathryn, Mullighan Charles, Dogan Ahmet, Armstrong Scott A, Mughal Tariq, Vergilio Jo-Anne, Labrecque Elaine, Erlich Rachel, Vietz Christine, Yelensky Roman, Stephens Philip J, Miller Vincent A, van den Brink Marcel R M, Otto Geoff A, Lipson Doron, Levine Ross L
Foundation Medicine, Cambridge, MA;
Leukemia Service, Department of Medicine, Human Oncology and Pathogenesis Program.
Blood. 2016 Jun 16;127(24):3004-14. doi: 10.1182/blood-2015-08-664649. Epub 2016 Mar 10.
The spectrum of somatic alterations in hematologic malignancies includes substitutions, insertions/deletions (indels), copy number alterations (CNAs), and a wide range of gene fusions; no current clinically available single assay captures the different types of alterations. We developed a novel next-generation sequencing-based assay to identify all classes of genomic alterations using archived formalin-fixed paraffin-embedded blood and bone marrow samples with high accuracy in a clinically relevant time frame, which is performed in our Clinical Laboratory Improvement Amendments-certified College of American Pathologists-accredited laboratory. Targeted capture of DNA/RNA and next-generation sequencing reliably identifies substitutions, indels, CNAs, and gene fusions, with similar accuracy to lower-throughput assays that focus on specific genes and types of genomic alterations. Profiling of 3696 samples identified recurrent somatic alterations that impact diagnosis, prognosis, and therapy selection. This comprehensive genomic profiling approach has proved effective in detecting all types of genomic alterations, including fusion transcripts, which increases the ability to identify clinically relevant genomic alterations with therapeutic relevance.
血液系统恶性肿瘤中的体细胞改变谱包括替换、插入/缺失(indel)、拷贝数改变(CNA)以及广泛的基因融合;目前临床上没有一种单一检测方法能够涵盖不同类型的改变。我们开发了一种基于新一代测序的新型检测方法,可使用存档的福尔马林固定石蜡包埋血液和骨髓样本,在临床相关的时间范围内以高精度识别所有类型的基因组改变,该检测在我们经临床实验室改进修正案认证且获得美国病理学家学会认可的实验室中进行。对DNA/RNA的靶向捕获和新一代测序能够可靠地识别替换、indel、CNA和基因融合,其准确性与专注于特定基因和基因组改变类型的低通量检测方法相似。对3696个样本的分析确定了影响诊断、预后和治疗选择的复发性体细胞改变。这种全面的基因组分析方法已被证明在检测所有类型的基因组改变(包括融合转录本)方面是有效的,这提高了识别具有治疗相关性的临床相关基因组改变的能力。