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Immunotherapy of thymic epithelial tumors: molecular understandings and clinical perspectives

期刊

MOLECULAR CANCER
卷 22, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12943-023-01772-4

关键词

Thymic epithelial tumors; Immunotherapy; Immune checkpoint inhibitors; PD-1; PD-L1; Immune-related adverse events

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Immunotherapy has become increasingly important in cancer treatment, particularly the use of PD-1 and PD-L1 inhibitors in thymic epithelial tumors. However, the high incidence of immune-related adverse events poses challenges and requires further understanding of the underlying mechanisms and development of effective prevention and management strategies.
Immunotherapy has emerged to play a rapidly expanding role in the treatment of cancers. Currently, many clinical trials of therapeutic agents are on ongoing with majority of immune checkpoint inhibitors (ICIs) especially programmed death receptor 1 (PD-1) and its ligand 1 (PD-L1) inhibitors. PD-1 and PD-L1, two main immune checkpoints, are expressed at high levels in thymic epithelial tumors (TETs) and could be predictors of the progression and immunotherapeutic efficacy of TETs. However, despite inspiring efficacy reported in clinical trials and clinical practice, significantly higher incidence of immune-related adverse events (irAEs) than other tumors bring challenges to the administration of ICIs in TETs. To develop safe and effective immunotherapeutic patterns in TETs, understanding the clinical properties of patients, the cellular and molecular mechanisms of immunotherapy and irAEs occurrence are crucial. In this review, the progress of both basic and clinical research on immune checkpoints in TETs, the evidence of therapeutic efficacy and irAEs based on PD-1 /PD-L1 inhibitors in TETs treatment are discussed. Additionally, we highlighted the possible mechanisms underlying irAEs, prevention and management strategies, the insufficiency of current research and some worthy research insights. High PD-1/PD-L1 expression in TETs provides a rationale for ICI use. Completed clinical trials have shown an encouraging efficacy of ICIs, despite the high rate of irAEs. A deeper mechanism understanding at molecular level how ICIs function in TETs and why irAEs occur will help maximize the immunotherapeutic efficacy while minimizing irAEs risks in TET treatment to improve patient prognosis.

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