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抗 PD-L1 治疗早期非小细胞肺癌中与反应和生存相关的增强增殖的特征。

A signature of enhanced proliferation associated with response and survival to anti-PD-L1 therapy in early-stage non-small cell lung cancer.

机构信息

Meyer Cancer Center, Weill Cornell Medicine and New York Presbyterian Hospital, New York, NY 10065, USA; Department of Cardiothoracic Surgery, Weill Cornell Medicine and New York Presbyterian Hospital, New York, NY 10065, USA.

Department of Physiology and Biophysics, Weill Cornell Medicine, New York, NY 10065, USA; Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY, USA.

出版信息

Cell Rep Med. 2024 Mar 19;5(3):101438. doi: 10.1016/j.xcrm.2024.101438. Epub 2024 Feb 23.

Abstract

In early-stage non-small cell lung cancer, the combination of neoadjuvant anti-PD-L1 and subablative stereotactic body radiation therapy (SBRT) is associated with higher rates of major pathologic response compared to anti-PD-L1 alone. Here, we identify a 140-gene set, enriched in genes characteristic of highly proliferating cells, associated with response to the dual therapy. Analysis of on-treatment transcriptome data indicate roles for T and B cells in response. The 140-gene set is associated with disease-free survival when applied to the combined trial arms. This 140-gene set identifies a subclass of tumors in all 7 of The Cancer Genome Atlas tumor types examined. Worse survival is associated with the 140-gene signature in 5 of these tumor types. Collectively, our data support that this 140-gene set, discovered in association with response to combined anti-PD-L1 and SBRT, identifies a clinically aggressive subclass of solid tumors that may be more likely to respond to immunotherapies.

摘要

在早期非小细胞肺癌中,与单独使用抗 PD-L1 相比,新辅助抗 PD-L1 和亚消融立体定向体部放射治疗(SBRT)的联合治疗与更高的主要病理缓解率相关。在这里,我们确定了一个 140 个基因集,这些基因富集了具有高增殖细胞特征的基因,与对双重治疗的反应相关。对治疗中转录组数据的分析表明 T 细胞和 B 细胞在反应中的作用。当应用于联合试验臂时,这 140 个基因集与无病生存相关。在所有 7 种经 TCGA 检测的肿瘤类型中,这 140 个基因集均可识别出亚类肿瘤。在其中 5 种肿瘤类型中,与 140 个基因特征相关的生存更差。总的来说,我们的数据支持这样一种观点,即与联合使用抗 PD-L1 和 SBRT 后的反应相关的这个 140 个基因集,可识别出具有临床侵袭性的实体肿瘤亚类,这些肿瘤可能更有可能对免疫疗法产生反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e878/10982989/b10aa4e2f3c0/fx1.jpg

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