Biomarkers of immunotherapy for non-small cell lung cancer

被引:4
作者
Shirasawa, Masayuki [1 ,2 ]
Yoshida, Tatsuya [1 ]
Ohe, Yuichiro [1 ]
机构
[1] Natl Canc Ctr, Dept Thorac Oncol, Chuo Ku, Tokyo, Japan
[2] Kitasato Univ, Sch Med, Dept Resp Med, Sagamihara, Kanagawa, Japan
关键词
biomarker; immunotherapy; non-small cell lung cancer; TERTIARY LYMPHOID STRUCTURES; TISSUE TMB TTMB; PD-L1; EXPRESSION; OPEN-LABEL; B-CELLS; CHEMOTHERAPY CHEMO; 1ST-LINE NIVOLUMAB; ADVANCED NSCLC; PLASMA-CELLS; DOCETAXEL;
D O I
10.1093/jjco/hyad134
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immunotherapy is revolutionizing the treatment of non-small cell lung cancer by targeting immune checkpoint proteins, including programmed death-1, programmed death ligand 1 and cytotoxic T-lymphocyte-associated antigen 4. Several immune checkpoint inhibitors, including programmed death ligand 1 inhibitors, programmed death-1 inhibitors and cytotoxic T-lymphocyte-associated antigen 4 inhibitors, were approved for the treatment of patients with advanced non-small cell lung cancer. Programmed death ligand 1 expression is currently the only predictive biomarker for immune checkpoint inhibitors to guide the treatment strategy in these patients. However, programmed death ligand 1 expression is not a perfect biomarker for predicting the efficacy of immunotherapy. Therefore, various biomarkers such as tumour mutation burden, tumour microenvironment, gut microbiome and T-cell receptor repertoire have been proposed to predict the efficacy of immunotherapy more accurately. Additionally, combining different biomarkers may provide a more accurate prediction of response to immunotherapy. This article reports the review of the latest evidence of the predictive marker of immunotherapy in patients with advanced non-small cell lung cancer.
引用
收藏
页码:13 / 22
页数:10
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