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首页> 外文期刊>Journal of immunotherapy >Advanced Non-Small Cell Lung Cancer Patients With Low Tumor Mutation Burden Might Derive Benefit From Immunotherapy
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Advanced Non-Small Cell Lung Cancer Patients With Low Tumor Mutation Burden Might Derive Benefit From Immunotherapy

机译:肿瘤突变负担低的先进的非小细胞肺癌患者可能会导致免疫疗法的益处

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摘要

The aim of this study is to investigate the association between tumor mutation burden (TMB) and survival in non-small cell lung cancer (NSCLC) patients with anti-programmed cell death protein 1 and anti-programmed death-ligand 1 blockade. Two retrospective cohorts and The Cancer Genome Atlas NSCLC data set were included in this study. The restricted cubic spline analysis was used to explore the association between TMB and survival. The cutoff values for TMB were determined by X-tile software. Primary outcomes were overall survival (OS). The associations between TMB and intratumor heterogeneity, number of segments, fraction of genome alterations, aneuploidy score, and T-cell populations were also investigated. In the restricted cubic spline plots, TMB showed an inverted U-shaped curve with OS. The median OS in the low TMB group was significantly longer than those in the medium TMB group. In The Cancer Genome Atlas NSCLC data set, low TMB was also associated with longer OS in comparison with medium TMB. Furthermore, NSCLC patients with low TMB had significantly lower intratumor heterogeneity, number of segments, fraction of genome alterations, aneuploidy score, T-helper type 2 (Th2) cells, and CD8(+)T cells, but higher levels of Th1 and Th17 cells. Low TMB might be a prognostic factor for NSCLC patients receiving anti-programmed cell death protein 1/programmed death-ligand 1 immunotherapy.
机译:本研究的目的是探讨肿瘤突变负担(TMB)与非小细胞肺癌(NSCLC)患者的肿瘤突变负荷(TMB)和生存期的关联,患有抗程序性细胞死亡蛋白1和反向死亡 - 配体1阻断。本研究包括两个回顾性群和癌症基因组ATLAS NSCLC数据集。限制的立方样条分析用于探讨TMB和生存之间的关联。 TMB的截止值由X-Tile软件确定。主要结果是总体生存(OS)。还研究了TMB和肿瘤内异质性的关联,区段数,基因组变化的分数,短倍性评分和T细胞群体。在限制的立方样条图中,TMB显示了与OS的倒U形曲线。低TMB组中的中位OS显着长于中TMB组中的OS。在癌症基因组Atlas NSCLC数据集中,与中TMB相比,低TMB也与较长的OS相关联。此外,具有低TMB的NSCLC患者具有显着降低的肠内异质性,段数,基因组变化的数量,基因倍数评分,T-辅助型2(TH2)细胞,以及CD8(+)T细胞,但较高的TH和TH17细胞。低TMB可能是接受抗程序性细胞死亡蛋白1 /编程死亡 - 配体1免疫疗法的NSCLC患者的预后因素。

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