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Clinical Application of Prognostic Gene Expression Signature in Fusion Gene-Negative Rhabdomyosarcoma: A Report from the Children's Oncology Group

机译:预后基因表达鉴定在融合基因阴性脉络膜瘤中的临床应用:儿童肿瘤学群的报告

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Purpose: Pediatric rhabdomyosarcoma (RMS) has two common histologic subtypes: embryonal (ERMS) and alveolar (ARMS). PAX-FOXO1 fusion gene status is a more reliable prognostic marker than alveolar histology, whereas fusion gene-negative (FN) ARMS patients are clinically similar to ERMS patients. A five-gene expression signature (MG5) previously identified two diverse risk groups within the fusion gene-negative RMS (FN-RMS) patients, but this has not been independently validated. The goal of this study was to test whether expression of the MG5 metagene, measured using a technical platform that can be applied to routine pathology material, would correlate with outcome in a new cohort of patients with FN-RMS.
机译:目的:儿科横纹肌肉瘤(RMS)具有两种常见的组织学亚型:胚胎(ERMS)和肺泡(臂)。 pax-foxo1融合基因状态是一种比肺泡组织学更可靠的预后标记物,而融合基因阴性(Fn)患者患者临床上与ERMS患者相似。 五基因表达签名(MG5)先前鉴定了融合基因负符号(FN-RMS)患者内的两种不同风险群体,但这尚未独立验证。 本研究的目标是测试使用可应用于常规病理材料的技术平台测量的Mg5比赛的表达,将与FN-RMS患者的新群体的结果相关。

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