Predictive biomarkers of response to immune checkpoint inhibitors

被引:2
|
作者
Sacramento Diaz-Carrasco, Maria [1 ]
Gonzalez-Haba, Eva [2 ]
Ines Garcia-Soler, Juana [1 ]
Espuny-Miro, Alberto [1 ]
机构
[1] Hosp Clin Univ Virgen de la Arrixaca, Serv Farm, Ctra Cartagena S-N, El Palmar 30120, Murcia, Spain
[2] Hosp Gregorio Maranon, Serv Farm, Madrid, Spain
关键词
Biomarkers; Immune checkpoint inhibitors; Immunotherapy; Programmed cell death-1 receptor; CELL LUNG-CANCER; CLINICAL-RESPONSE; ATEZOLIZUMAB; MULTICENTER; CARCINOMA; BLOCKADE; ASSAYS;
D O I
10.7399/fh.11328
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: The present paper provides a literature review aimed at identifying the tumor-dependent factors capable of influencing a subject's response to immune checkpoint inhibitors, with a special emphasis on those that may act as predictive biomarkers. Method: A search was performed of the terms biomarkers, PD-1, PD-L1, CTLA-4, and checkpoint inhibitors in the title and the abstract of the records in the PubMed database. Articles including relevant information on the tumor-dependent factors capable of influencing a subject's response of immune checkpoint inhibitors were selected. Priority was given to studies in humans (clinical trials and reviews) published between January 2015 and June 2019, in English and Spanish. Results: The literature review exposed the complex relationship that exists between the immune system and tumors. It also revealed that the factors capable of influencing a subject's response to immune checkpoint inhibitors are multiple, heterogeneous and ill understood, which makes it difficult to obtain simple and/or universal predictive biomarkers. Conclusions: The only biomarkers currently used in clinical practice include the expression of the programmed cell death ligand-1 and micro-satellite instability/deficient DNA mismatch repair, but their usefulness is limited. Tumor mutational burden and gene signatures associated to IFN-gamma could become useful biomarkers once determination techniques and cutoff points are systematized.
引用
收藏
页码:141 / 148
页数:8
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