Evolving therapies in advanced oesophago-gastric cancers and the increasing role of immunotherapy.
Gastroesophageal cancer
anti-PD-1
cytotoxic chemotherapy
esophageal cancer
esophagogastric cancer
gastric cancer
immunotherapy
novel agents
review
Journal
Expert review of anticancer therapy
ISSN: 1744-8328
Titre abrégé: Expert Rev Anticancer Ther
Pays: England
ID NLM: 101123358
Informations de publication
Date de publication:
05 2021
05 2021
Historique:
pubmed:
23
12
2020
medline:
4
3
2022
entrez:
22
12
2020
Statut:
ppublish
Résumé
Esophagogastric cancers remain a considerable health burden and among the top causes of global cancer-related deaths. Chemotherapy remains the cornerstone of treatment for patients with advanced disease. Doublet platinum/fluoropyrimidine therapy is established as first-line treatment with the option of adding a taxane in selected patients. Irinotecan, taxanes, and ramucirumab are approved as second-line treatments. Results from the trials KEYNOTE-059, ATTRACTION-2, and TAGS have established the use of immune checkpoint inhibitors and trifluridine/tipiracil as a third-line treatment. High PD-L1 expression, microsatellite instability, tumor mutational burden, and Epstein-Barr virus status may also be used to enrich for responses to immunotherapy. In this review, we discuss the outcome of recent trials in the later lines of therapy for esophagogastric cancer and place these in the context of current treatment paradigms. We also discuss the biology of esophagogastric cancers and how this might inform the development of new treatments. Finally, we comment on promising new drugs in development. Recent advances in the treatment of chemo-refractory esophagogastric cancer add to the improving survival of patients with this disease. Further research is needed to improve patient selection to therapies and the earlier incorporation of these agents in the treatment journey.
Identifiants
pubmed: 33349073
doi: 10.1080/14737140.2021.1866548
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM