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数量优势:从大型临床数据集预测对检查点抑制剂的反应。

Strength in numbers: predicting response to checkpoint inhibitors from large clinical datasets.

机构信息

Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany; German Cancer Consortium (DKTK), Heidelberg partner site, Heidelberg, Germany; German Center for Lung Research (DZL), Heidelberg partner site, Heidelberg, Germany.

Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany; German Center for Lung Research (DZL), Heidelberg partner site, Heidelberg, Germany.

出版信息

Cell. 2021 Feb 4;184(3):571-573. doi: 10.1016/j.cell.2021.01.008. Epub 2021 Jan 27.

DOI:10.1016/j.cell.2021.01.008
PMID:33508231
Abstract

The advent of immune checkpoint blockers for cancer therapy has spawned great interest in identifying molecular features reflecting the complexity of tumor immunity, which can subsequently be leveraged as predictive biomarkers. In a thorough big-data approach analyzing the largest series of homogenized molecular and clinical datasets, Litchfield et al. identified a set of genomic biomarkers that identifies immunotherapy responders across cancer types.

摘要

免疫检查点抑制剂在癌症治疗中的应用引发了人们极大的兴趣,促使人们去寻找反映肿瘤免疫复杂性的分子特征,这些特征随后可作为预测生物标志物加以利用。在一项对最大系列均质化分子和临床数据集进行全面大数据分析的研究中,Litchfield 等人确定了一组基因组生物标志物,可用于鉴定跨癌症类型的免疫治疗应答者。

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引用本文的文献

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Front Oncol. 2024 Nov 25;14:1483454. doi: 10.3389/fonc.2024.1483454. eCollection 2024.
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Tumour mutational burden: clinical utility, challenges and emerging improvements.肿瘤突变负担:临床实用性、挑战和新兴的改进。
Nat Rev Clin Oncol. 2024 Oct;21(10):725-742. doi: 10.1038/s41571-024-00932-9. Epub 2024 Aug 27.
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External quality assessment (EQA) for tumor mutational burden: results of an international IQN path feasibility pilot scheme.
肿瘤突变负荷的外部质量评估:国际 IQN 路径可行性试点计划的结果。
Virchows Arch. 2023 Feb;482(2):347-355. doi: 10.1007/s00428-022-03444-y. Epub 2022 Nov 10.
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Enhanced Antitumor Response to Immune Checkpoint Blockade Exerted by Cisplatin-Induced Mutagenesis in a Murine Melanoma Model.顺铂诱导的诱变在小鼠黑色素瘤模型中增强对免疫检查点阻断的抗肿瘤反应。
Front Oncol. 2021 Jul 6;11:701968. doi: 10.3389/fonc.2021.701968. eCollection 2021.