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Mutational Profile Evaluates Response and Survival to First‐Line Chemotherapy in Lung Cancer

机译:突变简介评估肺癌的一线化疗的反应和生存

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摘要

Evaluating the therapeutic response and survival of lung cancer patients receiving first‐line chemotherapy has always been difficult. Limited biomarkers for evaluation exist and as a result histology represents an empiric tool to guide therapeutic decision making. In this study, molecular signatures associated with response and long‐term survival of lung cancer patients receiving first‐line chemotherapy are discovered. Whole‐exome sequencing is performed on pretherapeutic tissue samples of 186 patients [145 non‐small cell lung cancer (NSCLC) and 41 small cell lung cancer (SCLC)]. On the basis of genomic alteration characteristics, NSCLC patients can be classified into four subtypes (C1–C4). The long‐term survival is similar among different subtypes. SCLC patients are also divided into four subtypes and significant difference in their progression free survival is revealed (P < 0.001). NSCLC patients can be divided into three subtypes (S1–S3) based on TMB. A trend of worse survival associated with higher TMB in subtype S3 than in S1+S2 is found. In contrast, no significant correlations between molecular subtype and therapeutic response are observed. In conclusion, this study identifies several molecular signatures associated with response and survival to first‐line chemotherapy in lung cancer.
机译:评估肺癌患者接受一线化疗的治疗反应和存活一直很困难。存在有限的评估生物标志物,并且由于组织学代表了指导治疗决策的经验工具。在该研究中,发现了与接受一线化疗的肺癌患者的反应和长期存活相关的分子鉴定。在186名患者的普形素质组织样品上进行全外膜测序[145非小细胞肺癌(NSCLC)和41个小细胞肺癌(SCLC)]。在基因组改变特征的基础上,NSCLC患者可以分为四种亚型(C1-C4)。在不同的亚型中,长期存活率类似。 SCLC患者还分为四个亚型,揭示了其进展自由存活的显着差异(P <0.001)。基于TMB,NSCLC患者可以分为三个亚型(S1-S3)。找到与亚型S3中较高TMB相关的更差的存活率比S1 + S2更差。相反,观察分子亚型和治疗反应之间的显着相关性。总之,本研究识别与肺癌一线化疗的反应和生存相关的几种分子鉴定。

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