Gastrointestinal Stromal Tumor: Challenges and Opportunities for a New Decade.
Apoptosis
/ drug effects
Drug Resistance, Neoplasm
/ drug effects
Gastrointestinal Stromal Tumors
/ epidemiology
Humans
Imatinib Mesylate
/ therapeutic use
Molecular Targeted Therapy
Naphthyridines
/ therapeutic use
Protein Kinase Inhibitors
/ therapeutic use
Proto-Oncogene Proteins c-kit
/ genetics
Pyrazoles
/ therapeutic use
Pyrroles
/ therapeutic use
Receptor, Platelet-Derived Growth Factor alpha
/ genetics
Triazines
/ therapeutic use
Urea
/ analogs & derivatives
Journal
Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN: 1557-3265
Titre abrégé: Clin Cancer Res
Pays: United States
ID NLM: 9502500
Informations de publication
Date de publication:
01 10 2020
01 10 2020
Historique:
received:
03
05
2020
revised:
26
05
2020
accepted:
25
06
2020
pubmed:
1
7
2020
medline:
26
11
2021
entrez:
1
7
2020
Statut:
ppublish
Résumé
Gastrointestinal stromal tumor (GIST) provides a paradigm to evaluate new molecularly targeted therapies and to identify structural and functional mechanisms for drug response and resistance. Drug development in GIST has successfully exploited the high reliance on KIT/PDGFRA oncogenic signaling as a therapeutic vulnerability. The recent arrival of avapritinib and ripretinib to the GIST arena has aimed to further improve on precision kinase inhibition and address tumor heterogeneity in imatinib-resistant GIST. The two main clinical challenges for the forthcoming years entail tumor eradication in patients with early-stage GIST, and maximization of tumor response in late-stage disease. To succeed, we will need to better understand the mechanisms behind adaptation to KIT inhibition and apoptosis evasion, tumor evolution after successive lines of treatment, and to explore clinically novel creative therapeutic strategies, with the overarching goal to tackle the intrinsic oncogenic complexity while minimizing adverse events.
Identifiants
pubmed: 32601076
pii: 1078-0432.CCR-20-1706
doi: 10.1158/1078-0432.CCR-20-1706
doi:
Substances chimiques
Naphthyridines
0
Protein Kinase Inhibitors
0
Pyrazoles
0
Pyrroles
0
Triazines
0
avapritinib
513P80B4YJ
Imatinib Mesylate
8A1O1M485B
Urea
8W8T17847W
ripretinib
9XW757O13D
Proto-Oncogene Proteins c-kit
EC 2.7.10.1
Receptor, Platelet-Derived Growth Factor alpha
EC 2.7.10.1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
5078-5085Informations de copyright
©2020 American Association for Cancer Research.