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A Mouse Model to Investigate the Role of Cancer-Associated Fibroblasts in Tumor Growth
Published on: December 22, 2020
Fibroblast growth factor therapies in biliary tract cancers: current and future state
Teerada Siripoon1, Conor O'Donnell1, Zhaohui Jin1
1Department of Oncology, Mayo Clinic, Rochester, MN, USA.
Introduction:
Cholangiocarcinoma is the rare and aggressive tumor with poor prognosis and limited therapeutic options. Recently, there have been promising developments in molecular targeted therapies for patients following the progression of first-line chemotherapy and immunotherapy combinations. Dysregulation of fibroblast Growth Factor Receptor (FGFR) signaling is significantly associated with tumorigenesis of intrahepatic cholangiocarcinoma and has been identified as a targetable alteration. This was possible through the discovery of crucial insights into the biochemical mechanisms and pathophysiology of the FGFR pathway.
Areas Covered:
This review summarizes the current state of FGFR targeted therapies, mechanisms of resistance, and future directions for FGFR-targeted therapies in patients with cholangiocarcinoma.
Expert Opinion:
Currently, pemigatinib and futibatinib are FDA approved FGFR-targeted therapies that have demonstrated remarkable responses. However, there is still a significant proportion of patients whose disease remains intrinsically resistant to treatment and most patients eventually develop secondary resistance after an initial response. Additionally, unique side effects of FGFR inhibitors may limit their efficacy in clinical practice and can have detrimental effects on quality of life. Several novel FGFR inhibitors are currently being investigated to overcome resistance mechanisms and reduce toxicities.
Insights
Fibroblast Growth Factor Receptor (FGFR) targeted therapies show promise for cholangiocarcinoma. However, resistance and side effects necessitate developing novel inhibitors to improve patient outcomes.
Area of Science:
- Oncology
- Molecular Biology
- Drug Development
Background:
- Cholangiocarcinoma (CCA) is a rare, aggressive cancer with limited treatment options.
- Fibroblast Growth Factor Receptor (FGFR) signaling dysregulation is implicated in intrahepatic cholangiocarcinoma (iCCA) tumorigenesis.
- FGFR pathway insights enable targeted therapeutic strategies.
Purpose of the Study:
- To review current FGFR-targeted therapies for cholangiocarcinoma.
- To discuss mechanisms of resistance to FGFR inhibitors.
- To explore future directions in FGFR-targeted treatment for CCA.
Main Methods:
- Literature review of current FGFR-targeted therapies.
- Analysis of resistance mechanisms.
- Evaluation of novel FGFR inhibitors in development.
Main Results:
- Pemigatinib and futibatinib are FDA-approved FGFR inhibitors with notable responses in CCA.
- Intrinsic and acquired resistance to FGFR inhibitors remain significant clinical challenges.
- Unique toxicities of FGFR inhibitors can impact patient quality of life.
Conclusions:
- FGFR-targeted therapies represent a significant advancement in cholangiocarcinoma treatment.
- Overcoming resistance and managing side effects are crucial for optimizing FGFR inhibitor efficacy.
- Ongoing research into novel FGFR inhibitors holds promise for improved therapeutic outcomes in CCA.
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