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Paper · 42881857

Molecularly Guided Therapy and the Tumor Microenvironment in Advanced Cholangiocarcinoma: Current Evidence and Emerging Strategies Targeting FGFR2, HER2, and IDH1 with Pemigatinib, Zanidatamab, and Ivosidenib.

Kawczak P and 1 other. J Clin Med, 2026.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Molecularly Guided Therapy and the Tumor Microenvironment in Advanced Cholangiocarcinoma: Current Evidence and Emerging Strategies Targeting FGFR2, HER2, and IDH1 with Pemigatinib, Zanidatamab, and Ivosidenib. Papers, record 42881857. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/42881857

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
Molecularly Guided Therapy and the Tumor Microenvironment in Advanced Cholangiocarcinoma: Current Evidence and Emerging Strategies Targeting FGFR2, HER2, and IDH1 with Pemigatinib, Zanidatamab, and Ivosidenib.
Journal
J Clin Med
Year
2026
Publication types
Journal Article, Review
Revised in PubMed
2026-10-20

Source PubMed

Authors2

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Kawczak PPiotrhttps://orcid.org/0000-0003-3902-2744
2Bączek TTomasz

Source PubMed

Topics0

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None in this release.

Grants0

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None in this release.

Trials0

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None in this release.

Comments and corrections0

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References298

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
142,137,650Hepatic Artery Infusion Chemotherapy for Cholangiocarcinoma in 2025.Liver Cancer2026https://conductscience.org/library/papers/42137650PubMed
237,710,362FGFR inhibitor resistance in cholangiocarcinoma: current understanding and future directions.Expert Opin Pharmacother2023https://conductscience.org/library/papers/37710362PubMed
332,168,869New and Emerging Systemic Therapeutic Options for Advanced Cholangiocarcinoma.Cells2020https://conductscience.org/library/papers/32168869PubMed
442,293,741Lipid nanoparticles and extracellular vesicles: emerging cell free therapeutic platforms for hepatobiliary cancers.Front Cell Dev Biol2026https://conductscience.org/library/papers/42293741PubMed
526,258,846Genomic spectra of biliary tract cancer.Nat Genet2015https://conductscience.org/library/papers/26258846PubMed
639,438,389Correction: Ivosidenib: A Review in Advanced Cholangiocarcinoma.Target Oncol2025https://conductscience.org/library/papers/39438389PubMed
730,905,548Biologics, Immunotherapy, and Future Directions in the Treatment of Advanced Cholangiocarcinoma.Clin Colorectal Cancer2019https://conductscience.org/library/papers/30905548PubMed
832,416,072Ivosidenib in IDH1-mutant, chemotherapy-refractory cholangiocarcinoma (ClarIDHy): a multicentre, randomised, double-blind, placebo-controlled, phase 3 study.Lancet Oncol2020https://conductscience.org/library/papers/32416072PubMed
925,162,885Updating cost-effectiveness--the curious resilience of the $50,000-per-QALY threshold.N Engl J Med2014https://conductscience.org/library/papers/25162885PubMed
1036,102,999Population pharmacokinetics of zanidatamab, an anti-HER2 biparatopic antibody, in patients with advanced or metastatic cancer.Cancer Chemother Pharmacol2022https://conductscience.org/library/papers/36102999PubMed

Cited by0

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Genes0

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None in this release.

Drugs0

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None in this release.

Data0

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None in this release.

Data dates

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PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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