Combined hepatocellular carcinoma and cholangiocarcinoma

disease
On this page

Also known as carcinoma of liver and intrahepatic biliary tractcarcinoma of the liver and intrahepatic biliary tractCholangiohepatomacombined hepatocellular cancer and cholangiocarcinoma (bile duct cancer)combined hepatocellular cancer and intrahepatic bile duct cancer (cholangiocarcinoma)Hepatocholangiocarcinomaliver and intrahepatic biliary tract carcinomaMixed hepatocellular cholangiocarcinoma

Summary

Combined hepatocellular carcinoma and cholangiocarcinoma (MONDO:0044791) is a cancer and 5 clinical trials. Top therapeutic interventions include cisplatin. A subtype of adenocarcinoma of gallbladder and extrahepatic biliary tract — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Classification: Cancer
  • Prevalence: Unknown (Worldwide) [Orphanet-validated]
  • Clinical trials: 5

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namecombined hepatocellular carcinoma and cholangiocarcinoma
Mondo IDMONDO:0044791
Orphanet529852
ICD-111097637010, 1600108866, 894488488
NCITC3828
SNOMED CT274902006
UMLSC0221287
MedGen113160
GARD0022200
Is cancer (heuristic)yes

Also known as: carcinoma of liver and intrahepatic biliary tract · carcinoma of the liver and intrahepatic biliary tract · Cholangiohepatoma · combined hepatocellular cancer and cholangiocarcinoma (bile duct cancer) · combined hepatocellular cancer and intrahepatic bile duct cancer (cholangiocarcinoma) · combined hepatocellular carcinoma and cholangiocarcinoma · Hepatocholangiocarcinoma · liver and intrahepatic biliary tract carcinoma · Mixed hepatocellular cholangiocarcinoma

Data availability: 2 cell lines.

Disease family

This is a subtype of adenocarcinoma of gallbladder and extrahepatic biliary tract. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease by body system or component › digestive system disorderdigestive system cancerliver cancerbiliary tract cancerbile duct cancerbile duct carcinomaextrahepatic bile duct carcinoma › extrahepatic bile duct adenocarcinoma › adenocarcinoma of gallbladder and extrahepatic biliary tractcombined hepatocellular carcinoma and cholangiocarcinoma

Related subtypes (1): cholangiocarcinoma

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 5.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified3
PHASE22

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05211323PHASE2ACTIVE_NOT_RECRUITINGA Study to Determine Whether Chemotherapy and Atezolizumab is Better Than Chemotherapy, Bevacizumab and Atezolizumab in Patients With Advanced Liver Cancer
NCT07105748PHASE2RECRUITINGHAIC Combined With Camrelizumab Plus Rivoceranib for Advanced Mixed Hepatocellular-cholangiocarcinoma (HCC-CCA)
NCT06541652Not specifiedRECRUITINGA French Multicenter Observational Retrospective Study of Rare Primary Liver Cancers
NCT06849180Not specifiedRECRUITINGNovel Subtypes and Treatment Strategies of Patients with Unresectable Combined Hepatocellular Cholangiocarcinoma Based on Multimodal Data
NCT02762721Not specifiedCOMPLETEDAnalysis of Oncogenes in Intrahepatic Cholangiocarcinoma or Mixed Hepatocellular-Cholangiocarcinoma in Tumor Tissue Samples

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
CISPLATIN41