Reeser Julie W, Martin Dorrelyn, Miya Jharna, Kautto Esko A, Lyon Ezra, Zhu Eliot, Wing Michele R, Smith Amy, Reeder Matthew, Samorodnitsky Eric, Parks Hannah, Naik Karan R, Gozgit Joseph, Nowacki Nicholas, Davies Kurtis D, Varella-Garcia Marileila, Yu Lianbo, Freud Aharon G, Coleman Joshua, Aisner Dara L, Roychowdhury Sameek
Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Ariad Pharmaceuticals, Cambridge, Massachusetts.
J Mol Diagn. 2017 Sep;19(5):682-696. doi: 10.1016/j.jmoldx.2017.05.006. Epub 2017 Aug 9.
Kinase gene fusions are important drivers of oncogenic transformation and can be inhibited with targeted therapies. Clinical grade diagnostics using RNA sequencing to detect gene rearrangements in solid tumors are limited, and the few that are available require prior knowledge of fusion break points. To address this, we have analytically validated a targeted RNA sequencing assay (OSU-SpARKFuse) for fusion detection that interrogates complete transcripts from 93 kinase and transcription factor genes. From a total of 74 positive and 36 negative control samples, OSU-SpARKFuse had 93.3% sensitivity and 100% specificity for fusion detection. Assessment of repeatability and reproducibility revealed 96.3% and 94.4% concordance between intrarun and interrun technical replicates, respectively. Application of this assay on prospective patient samples uncovered OLFM4 as a novel RET fusion partner in a small-bowel cancer and led to the discovery of a KLK2-FGFR2 fusion in a patient with prostate cancer who subsequently underwent treatment with a pan-fibroblast growth factor receptor inhibitor. Beyond fusion detection, OSU-SpARKFuse has built-in capabilities for discovery research, including gene expression analysis, detection of single-nucleotide variants, and identification of alternative splicing events.
激酶基因融合是致癌转化的重要驱动因素,可通过靶向治疗加以抑制。利用RNA测序检测实体瘤中基因重排的临床级诊断方法有限,且现有的少数方法需要预先了解融合断点。为解决这一问题,我们已通过分析验证了一种用于融合检测的靶向RNA测序检测方法(OSU-SpARKFuse),该方法可对93个激酶和转录因子基因的完整转录本进行检测。在总共74个阳性和36个阴性对照样本中,OSU-SpARKFuse在融合检测方面的灵敏度为93.3%,特异性为100%。对重复性和再现性的评估显示,批内和批间技术重复之间的一致性分别为96.3%和94.4%。将该检测方法应用于前瞻性患者样本,发现OLFM4是小肠癌中一种新的RET融合伴侣,并在一名前列腺癌患者中发现了KLK2-FGFR2融合,该患者随后接受了泛成纤维细胞生长因子受体抑制剂治疗。除融合检测外,OSU-SpARKFuse还具备用于探索性研究的内置功能,包括基因表达分析、单核苷酸变异检测和可变剪接事件识别。