Journal Article (Review Article) DKFZ-2025-00379

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Molecular subtypes of intrahepatic cholangiocarcinoma.

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2025
Elsevier Science Amsterdam [u.a.]

Trends in molecular medicine 31(8), 755-769 () [10.1016/j.molmed.2025.01.008]
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Abstract: Intrahepatic cholangiocarcinoma (iCCA) presents in two clinically distinct subtypes: large duct (LD-iCCA) and small duct (SD-iCCA). These subtypes exhibit significant molecular, genetic, and histopathological differences that impact patient prognosis and treatment responsiveness. This review advocates for a subtype-specific approach to iCCA research and clinical management, including tailored therapeutic strategies that consider distinct genetic profiles and tumor microenvironments. Current therapeutic approaches hold promise, yet efficacy varies by subtype. Additionally, subtype-specific molecular diagnostics, including DNA methylation-based classifiers and transcriptomic sequencing, have shown potential in refining iCCA subclassification, thereby guiding precision medicine efforts. This article outlines existing clinical trials, key research trajectories, and future directions for developing more effective subtype-adapted therapies for iCCA.

Keyword(s): clinical trial ; intrahepatic cholangiocarcinoma ; molecular targeted therapy ; mutation ; survival ; translational research

Classification:

Note: #EA:A430#LA:A430# / 2025 Aug;31(8):755-769

Contributing Institute(s):
  1. NWG-KKE Translationale Chirurgische Onkologie (A430)
Research Program(s):
  1. 311 - Zellbiologie und Tumorbiologie (POF4-311) (POF4-311)

Appears in the scientific report 2025
Database coverage:
Medline ; BIOSIS Previews ; BIOSIS Reviews Reports And Meetings ; Clarivate Analytics Master Journal List ; Current Contents - Clinical Medicine ; Current Contents - Life Sciences ; Ebsco Academic Search ; Essential Science Indicators ; IF >= 10 ; JCR ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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 Record created 2025-02-18, last modified 2025-08-27



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