Endometrial transitional cell carcinoma

disease
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Summary

Endometrial transitional cell carcinoma (MONDO:0002832) is a cancer and 5 clinical trials. Top therapeutic interventions include nintedanib, brivanib alaninate, and dalantercept. A subtype of endometrial carcinoma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Classification: Cancer
  • Clinical trials: 5

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameendometrial transitional cell carcinoma
Mondo IDMONDO:0002832
DOIDDOID:4005
NCITC40154
UMLSC1516864
MedGen273232
GARD0023259
Is cancer (heuristic)yes

Also known as: endometrial transitional cell carcinoma

Disease family

This is a subtype of endometrial 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 by etiologic mechanism › cancer or benign tumorneoplastic disease or syndromeneoplasmcancerreproductive system cancerfemale reproductive organ canceruterine canceruterine carcinomaendometrial carcinomaendometrial transitional cell carcinoma

Related subtypes (6): uterine corpus endometrial carcinoma, endometrium carcinoma in situ, endometrium adenocarcinoma, endometrial small cell carcinoma, endometrial squamous cell carcinoma, endometrial undifferentiated 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: 5.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE24
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT02834013PHASE2ACTIVE_NOT_RECRUITINGNivolumab and Ipilimumab in Treating Patients With Rare Tumors
NCT00888173PHASE2COMPLETEDBrivanib Alaninate in Treating Patients With Recurrent or Persistent Endometrial Cancer
NCT01225887PHASE2COMPLETEDNintedanib in Treating Patients With Recurrent or Persistent Endometrial Cancer
NCT01642082PHASE2COMPLETEDDalantercept in Treating Patients With Recurrent or Persistent Endometrial Cancer
NCT01440998PHASE1COMPLETEDDasatinib, Paclitaxel, and Carboplatin in Treating Patients With Stage III-IV or Recurrent Endometrial Cancer

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
NINTEDANIB41
BRIVANIB ALANINATE31
DALANTERCEPT31