TY - JOUR
T1 - Novel and emerging targets for cholangiocarcinoma progression
T2 - therapeutic implications
AU - Kankeu Fonkoua, Lionel A.
AU - Serrano Uson Junior, Pedro Luiz
AU - Mody, Kabir
AU - Mahipal, Amit
AU - Borad, Mitesh J.
AU - Roberts, Lewis R.
N1 - Funding Information:
This manuscript was supported by the Mayo Clinic Hepatobiliary SPORE (NIH NCI P50CA210964) and the Mayo Clinic Center for Clinical and Translational Science (NIH NCATS UL1 TR002377) grants.
Publisher Copyright:
© 2022 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2022
Y1 - 2022
N2 - Introduction: 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. Areas covered: : 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. Expert Opinion: : 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.
AB - Introduction: 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. Areas covered: : 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. Expert Opinion: : 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.
KW - Cholangiocarcinoma
KW - fibroblast growth factor receptor (FGFR)
KW - immunotherapy
KW - isocitrate dehydrogenase 1 (IDH1)
KW - targeted therapy
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U2 - 10.1080/14728222.2022.2029412
DO - 10.1080/14728222.2022.2029412
M3 - Review article
C2 - 35034558
AN - SCOPUS:85123789521
SN - 1472-8222
VL - 26
SP - 79
EP - 92
JO - Expert Opinion on Therapeutic Targets
JF - Expert Opinion on Therapeutic Targets
IS - 1
ER -