Novel and emerging targets for cholangiocarcinoma progression: therapeutic implications.
Cholangiocarcinoma
fibroblast growth factor receptor (FGFR)
immunotherapy
isocitrate dehydrogenase 1 (IDH1)
targeted therapy
Journal
Expert opinion on therapeutic targets
ISSN: 1744-7631
Titre abrégé: Expert Opin Ther Targets
Pays: England
ID NLM: 101127833
Informations de publication
Date de publication:
01 2022
01 2022
Historique:
pubmed:
18
1
2022
medline:
3
3
2022
entrez:
17
1
2022
Statut:
ppublish
Résumé
Cholangiocarcinoma (CCA) is a heterogeneous group of aggressive biliary malignancies. While surgery and liver transplantation are the only potentially curative modalities for early-stage disease, limited options are available for most patients with incurable-stage disease. Survival outcomes remain dismal. Recent molecular profiling efforts have led to improved understanding of the genomic landscape of CCA and to the identification of subgroups with distinct diagnostic, prognostic, and therapeutic implications. : We provide an updated review and future perspectives on features of cholangiocarcinogenesis that can be translated into therapeutic biomarkers and targets. We highlight the critical studies that have established current systemic chemotherapy and targeted therapeutics, while elaborating on novel targeted and immunotherapeutic approaches in development. Relevant literature and clinical studies were identified by searching PubMed and www.ClinicalTrials.gov. : While therapies targeting the various molecular subgroups of CCA are rapidly emerging and changing treatment paradigms, their success has been limited by the genetic heterogeneity of CCA and the plasticity of the targets. Novel strategies aiming to combine immunotherapy, chemotherapy, and molecularly targeted therapeutics will be required to offer durable clinical benefit and maximize survival.
Identifiants
pubmed: 35034558
doi: 10.1080/14728222.2022.2029412
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
79-92Subventions
Organisme : NCI NIH HHS
ID : P50 CA210964
Pays : United States