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Semin Immunopathol ; 45(1): 29-41, 2023 01.
Article in English | MEDLINE | ID: mdl-36414693

ABSTRACT

First-line immunotherapy in non-small-cell lung cancer largely improved patients' survival. PD-L1 testing is required before immune checkpoint inhibitor initiation. However, this biomarker fails to accurately predict patients' response. On the other hand, immunotherapy exposes patients to immune-related toxicity, the mechanisms of which are still unclear. Hence, there is an unmet need to develop clinically approved predictive biomarkers to better select patients who will benefit the most from immune checkpoint inhibitors and improve risk management. Single-cell technologies provide unprecedented insight into the tumor and its microenvironment, leading to the discovery of immune cells involved in immune checkpoint inhibitor response or toxicity. In this review, we will underscore the potential of the single-cell approach to identify candidate biomarkers improving non-small-cell lung cancer patients' care.


Subject(s)
Carcinoma, Non-Small-Cell Lung , Lung Neoplasms , Humans , Carcinoma, Non-Small-Cell Lung/diagnosis , Carcinoma, Non-Small-Cell Lung/etiology , Carcinoma, Non-Small-Cell Lung/therapy , Lung Neoplasms/therapy , Lung Neoplasms/drug therapy , Immune Checkpoint Inhibitors/therapeutic use , Biomarkers , Immunotherapy , B7-H1 Antigen/therapeutic use , Biology , Biomarkers, Tumor/therapeutic use , Tumor Microenvironment
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