Evidence map›Paper›PMID 41226789›Full record

ReviewInternational journal of molecular sciences2025

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

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

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Lily DarmanDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN 46617, USA.
Quinn KaurichDepartment of Surgery, Indiana University School of Medicine, South Bend, IN 46617, USA.ORCID 0000-0002-4974-898X
Md Sazzad HassanDepartment of Surgery, Indiana University School of Medicine, South Bend, IN 46617, USA.ORCID 0000-0001-6309-9616
Urs von HolzenDepartment of Surgery, Indiana University School of Medicine, South Bend, IN 46617, USA.
Niranjan AwasthiDepartment of Surgery, Indiana University School of Medicine, South Bend, IN 46617, USA.

Funding

Indiana University School of Medicine 23-817-16
6 · The paper itself

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.

Indexed as

Bile Duct NeoplasmsCholangiocarcinomaIsocitrate DehydrogenaseMolecular Targeted TherapyReceptor, Fibroblast Growth Factor, Type 2Antineoplastic AgentsHumansAntineoplastic AgentsFGFR2 protein, humanIDH1 protein, humanIsocitrate DehydrogenaseReceptor, Fibroblast Growth Factor, Type 2cholangiocarcinomaFGFRIDHKRAStargeted therapies

Identifiers

PMID41226789
PMCPMC12608419

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.