PD-1 and PD-L1 inhibitors in oesophago-gastric cancers.
Antibodies, Monoclonal, Humanized
/ pharmacology
Antineoplastic Agents, Immunological
/ pharmacology
Antineoplastic Combined Chemotherapy Protocols
/ pharmacology
B7-H1 Antigen
/ antagonists & inhibitors
Chemotherapy, Adjuvant
/ methods
Disease-Free Survival
Esophageal Neoplasms
/ immunology
Esophagectomy
Esophagogastric Junction
/ immunology
Gastrectomy
Humans
Nivolumab
/ pharmacology
Programmed Cell Death 1 Receptor
/ antagonists & inhibitors
Randomized Controlled Trials as Topic
Signal Transduction
/ drug effects
Stomach Neoplasms
/ immunology
Immune checkpoint inhibitors
Immunotherapy
Oesophageal-gastric cancer
PD-1
PD-L1
Journal
Cancer letters
ISSN: 1872-7980
Titre abrégé: Cancer Lett
Pays: Ireland
ID NLM: 7600053
Informations de publication
Date de publication:
28 01 2020
28 01 2020
Historique:
received:
08
09
2019
revised:
18
10
2019
accepted:
22
10
2019
pubmed:
2
11
2019
medline:
1
7
2020
entrez:
1
11
2019
Statut:
ppublish
Résumé
Oesophago-gastric cancers (OGCs) are aggressive tumours. While better peri-operative strategies, increased number of cytotoxic agents and availability of targeted therapies have improved survival, there remains an unmet need for novel treatment approaches. Immune checkpoint inhibitors (ICIs) have marked a new era in cancer management with unprecedented results in several malignancies. Although OGC lagged behind other solid tumours, evidence has increasingly accumulated supporting the contention that modulation of the anti-cancer host immune response may be beneficial for at least some patients. Many trials have been completed in Eastern and Western countries, some of these leading to the approval of ICIs in the refractory setting, and favorable opinion from regulatory agencies is expected also in treatment-naïve, advanced OGC. Furthermore, studies are evaluating ICIs in the early stage setting and exploring the potential of combination treatments. In this article we discuss the biological bases underlying the successful development of ICIs in OGC and review the available data on PD-1 and PD-L1 monoclonal antibodies in this disease. Also, we present ongoing clinical trials of these ICIs that could shape the future treatment landscape of OGC.
Identifiants
pubmed: 31669518
pii: S0304-3835(19)30539-7
doi: 10.1016/j.canlet.2019.10.036
pii:
doi:
Substances chimiques
Antibodies, Monoclonal, Humanized
0
Antineoplastic Agents, Immunological
0
B7-H1 Antigen
0
CD274 protein, human
0
PDCD1 protein, human
0
Programmed Cell Death 1 Receptor
0
Nivolumab
31YO63LBSN
pembrolizumab
DPT0O3T46P
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
142-150Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.