# Expanding Horizons in Cholangiocarcinoma: Emerging Targets Beyond FGFR2 and IDH1

**Authors:** Lily Darman, Quinn Kaurich, Md Sazzad Hassan, Urs von Holzen, Niranjan Awasthi

PMC · DOI: 10.3390/ijms262110755 · International Journal of Molecular Sciences · 2025-11-05

## TL;DR

This review explores new treatment targets for cholangiocarcinoma beyond the currently approved therapies, highlighting ongoing research to improve patient outcomes.

## Contribution

The paper provides a comprehensive overview of emerging molecular targets and therapies for cholangiocarcinoma.

## Key findings

- Currently approved targeted therapies include ivosidenib, pemigatinib, infigratinib, futibatinib, and durvalumab.
- Multiple molecular pathways such as p53/MDM2, JAK/STAT, and KRAS are being investigated for new therapeutic strategies.
- Further research is needed to improve treatment options and outcomes for patients with advanced cholangiocarcinoma.

## Abstract

Cholangiocarcinoma (CCA) is a biliary tract cancer that accounts for approximately 3% of all gastrointestinal cancers. CCA is a “silent” disease that remains undetected for a long period of time, often presenting at an advanced stage with minimal treatment options and a poor prognosis. Advanced CCA remains largely inoperable, and combination gemcitabine plus cisplatin (GemCis) chemotherapy remains the standard treatment for patients affected by this disease. There is a desperate need for new therapeutic alternatives, and extensive research is ongoing to address this gap. Targeted therapies represent a rapidly expanding area of cancer treatment and are currently under active investigation in CCA. The FDA has approved the targeted therapies ivosidenib, pemigatinib, infigratinib, and futibatinib, as well as the immunotherapy durvalumab, for patients with CCA in recent years. Several other therapeutic strategies are still under investigation, targeting molecular pathways including p53/MDM2, JAK/STAT, KRAS, HER2, VEGFR, PDGFR, MET, ALK, MAPK, PI3K/AKT, BRAF, and DNA damage repair signaling. While several promising advancements have been made, further research is required to improve outcomes for patients with CCA. This review provides an up-to-date, comprehensive overview of currently approved targeted therapies in CCA, as well as those under investigation.

## Linked entities

- **Genes:** TP53 (tumor protein p53) [NCBI Gene 7157], MDM2 (MDM2 proto-oncogene) [NCBI Gene 4193], jak (Janus kinase) [NCBI Gene 778659], SOAT1 (sterol O-acyltransferase 1) [NCBI Gene 6646], KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845], ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064], KDR (kinase insert domain receptor) [NCBI Gene 3791], PDGFRB (platelet derived growth factor receptor beta) [NCBI Gene 5159], MET (MET proto-oncogene, receptor tyrosine kinase) [NCBI Gene 4233], ALK (ALK receptor tyrosine kinase) [NCBI Gene 238], MAPK (mitogen activated kinase-like protein) [NCBI Gene 7446652], PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290], AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207], BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673]
- **Chemicals:** ivosidenib (PubChem CID 71657455), pemigatinib (PubChem CID 86705695), infigratinib (PubChem CID 53235510), futibatinib (PubChem CID 71621331), gemcitabine (PubChem CID 60750), cisplatin (PubChem CID 5460033)
- **Diseases:** cholangiocarcinoma (MONDO:0019087), CCA (MONDO:0007363)

## Full-text entities

- **Genes:** IDH1 (isocitrate dehydrogenase (NADP(+)) 1) [NCBI Gene 3417] {aka HEL-216, HEL-S-26, IDCD, IDH, IDP, IDPC}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, KDR (kinase insert domain receptor) [NCBI Gene 3791] {aka CD309, FLK1, VEGFR, VEGFR2}, PDGFRB (platelet derived growth factor receptor beta) [NCBI Gene 5159] {aka CD140B, IBGC4, IMF1, JTK12, KOGS, OPDKD}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845] {aka 'C-K-RAS, C-K-RAS, CFC2, K-RAS2A, K-RAS2B, K-RAS4A}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}, FGFR2 (fibroblast growth factor receptor 2) [NCBI Gene 2263] {aka BBDS, BEK, BFR-1, CD332, CEK3, CFD1}, SLTM (SAFB like transcription modulator) [NCBI Gene 79811] {aka Met}, MDM2 (MDM2 proto-oncogene) [NCBI Gene 4193] {aka ACTFS, HDMX, LSKB, hdm2}, ALK (ALK receptor tyrosine kinase) [NCBI Gene 238] {aka ALK1, CD246, NBLST3}
- **Diseases:** biliary tract cancer (MESH:D001661), CCA (MESH:D018281), cancer (MESH:D009369), gastrointestinal cancers (MESH:D005770)
- **Chemicals:** durvalumab (MESH:C000613593), pemigatinib (MESH:C000705477), cisplatin (MESH:D002945), futibatinib (MESH:C000713257), ivosidenib (MESH:C000627630), GemCis (-), gemcitabine (MESH:D000093542), infigratinib (MESH:C568950)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

143 references — full list in the complete paper: https://tomesphere.com/paper/PMC12608419/full.md

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Source: https://tomesphere.com/paper/PMC12608419