Recent developments in PD-1/PD-L1 blockade research for gastroesophageal malignancies

Gastroesophageal cancers (GECs) comprise malignancies in the stomach, esophagus, and gastroesophageal junction. Despite ongoing improvements in chemoradiotherapy, the clinical outcomes of GEC have not significantly improved over the years, and treatment remains challenging. Immune checkpoint inhibit...

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Published inFrontiers in immunology Vol. 13; p. 1043517
Main Authors Chen, Meng, Li, Chenyan, Sun, Mingjun, Li, Yiling, Sun, Xuren
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 24.11.2022
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Summary:Gastroesophageal cancers (GECs) comprise malignancies in the stomach, esophagus, and gastroesophageal junction. Despite ongoing improvements in chemoradiotherapy, the clinical outcomes of GEC have not significantly improved over the years, and treatment remains challenging. Immune checkpoint inhibitors (ICIs) have been the subject of clinical trials worldwide for several years. Encouraging results have been reported in different countries, but further research is required to apply ICIs in the clinical care of patients with GEC. This review summarizes completed and ongoing clinical trials with programmed death 1 (PD-1)/programmed death-ligand 1 (PD-L1) pathway blockers in GEC and current biomarkers used for predicting PD-1/PD-L1 blockade efficacy. This review captures the main findings of PD-1/PD-L1 antibodies combined with chemotherapy as an effective first-line treatment and a monotherapy in second-line or more treatment and in maintenance therapy. This review aims to provide insight that will help guide future research and clinical trials, thereby improving the outcomes of patients with GEC.
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Reviewed by: Peng Jin, Seventh Medical Center of PLA General Hospital, China; Thanh Huong Phung, Hanoi University of Pharmacy, Vietnam
Edited by: Qi Yang, Rutgers, The State University of New Jersey, United States
This article was submitted to Cancer Immunity and Immunotherapy, a section of the journal Frontiers in Immunology
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2022.1043517