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Mutational Profile of Malignant Pleural Mesothelioma (MPM) in the Phase II RAMES Study

机译:II期举例研究中的恶性胸膜间皮瘤(MPM)的突变概况

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摘要

Malignant pleura Mesothelioma (MPM) is an aggressive cancer arising from the mesothelial cells of the pleura. About 80% of mesothelioma cases are linked to asbestos exposure; the remainder may be related to prior chest radiation, genetic predisposition or spontaneous occurrence. Understanding the genetic alterations that drive MPM is critical for successful development of diagnostics, prognostics and personalized therapeutic modalities. Because MPM is rare, genomic studies are limited and have typically involved a small number of samples. The aim of our study was to understand the mutational landscape of MPM. Our analysis identified significantly mutated genes. This study on a rare tumor type will be important for patients “in real life”.
机译:恶性胸膜间皮瘤(MPM)是胸膜间皮细胞产生的侵略性癌症。大约80%的间皮瘤病例与石棉暴露有关;其余部分可能与先前的胸部辐射,遗传易感性或自发发生有关。了解推动MPM的遗传改变对于成功开发诊断,预测和个性化治疗方式至关重要。因为MPM是罕见的,基因组研究是有限的,并且通常涉及少量样品。我们研究的目的是了解MPM的突变景观。我们的分析鉴定了显着突变的基因。本研究对罕见的肿瘤类型对患者“在现实生活中”至关重要。

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