Gallbladder squamous cell carcinoma

disease
On this page

Also known as epidermoid carcinoma of gallbladderepidermoid carcinoma of the gallbladderepidermoid gallbladder carcinomagall bladder squamous cell carcinomagallbladder squamous cell cancersquamous cell carcinoma of gallbladdersquamous cell carcinoma of the gallbladdersquamous cell gallbladder carcinoma

Summary

Gallbladder squamous cell carcinoma (MONDO:0006220) is a cancer and 1 clinical trial. Top therapeutic interventions include sorafenib. A subtype of gallbladder carcinoma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Classification: Cancer
  • Clinical trials: 1

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namegallbladder squamous cell carcinoma
Mondo IDMONDO:0006220
EFOEFO:1000267
DOIDDOID:5535
NCITC9170
UMLSC0279658
MedGen83539
GARD0024336
Anatomy (UBERON)UBERON:0002110
Is cancer (heuristic)yes

Also known as: epidermoid carcinoma of gallbladder · epidermoid carcinoma of the gallbladder · epidermoid gallbladder carcinoma · gall bladder squamous cell carcinoma · gallbladder squamous cell cancer · gallbladder squamous cell carcinoma · squamous cell carcinoma of gallbladder · squamous cell carcinoma of the gallbladder · squamous cell gallbladder carcinoma

Disease family

This is a subtype of gallbladder carcinoma. 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 › human disease › disease by body system or component › digestive system disorderdigestive system cancergallbladder cancergallbladder carcinomagallbladder squamous cell carcinoma

Related subtypes (4): gall bladder carcinoma in situ, gallbladder adenocarcinoma, gallbladder small cell neuroendocrine carcinoma, undifferentiated gallbladder carcinoma

Subtypes (1): gallbladder adenosquamous carcinoma

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: 1.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00238212PHASE2COMPLETEDS0514 Sorafenib in Treating Patients With Unresectable or Metastatic Gallbladder Cancer or Cholangiocarcinoma

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
SORAFENIB41