Molecular profiling identifies targeted therapy opportunities in pediatric solid cancer

医学 靶向治疗 肿瘤科 内科学 融合基因 中期分析 临时的 实体瘤 癌症 临床试验 基因 生物化学 历史 考古 化学
作者
Alanna J. Church,Laura Corson,Pei‐Chi Kao,Alma Imamović,Deirdre Reidy,Duong Doan,Wenjun Kang,Navin Pinto,Luke Maese,Theodore W. Laetsch,AeRang Kim,Susan I. Colace,Margaret E. Macy,Mark A. Applebaum,Rochelle Bagatell,Amit J. Sabnis,Daniel A. Weiser,Julia Glade Bender,Alan C. Homans,John Hipps
出处
期刊:Nature Medicine [Nature Portfolio]
卷期号:28 (8): 1581-1589 被引量:39
标识
DOI:10.1038/s41591-022-01856-6
摘要

To evaluate the clinical impact of molecular tumor profiling (MTP) with targeted sequencing panel tests, pediatric patients with extracranial solid tumors were enrolled in a prospective observational cohort study at 12 institutions. In the 345-patient analytical population, median age at diagnosis was 12 years (range 0–27.5); 298 patients (86%) had 1 or more alterations with potential for impact on care. Genomic alterations with diagnostic, prognostic or therapeutic significance were present in 61, 16 and 65% of patients, respectively. After return of the results, impact on care included 17 patients with a clarified diagnostic classification and 240 patients with an MTP result that could be used to select molecularly targeted therapy matched to identified alterations (MTT). Of the 29 patients who received MTT, 24% had an objective response or experienced durable clinical benefit; all but 1 of these patients received targeted therapy matched to a gene fusion. Of the diagnostic variants identified in 209 patients, 77% were gene fusions. MTP with targeted panel tests that includes fusion detection has a substantial clinical impact for young patients with solid tumors.

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