Infiltrating bladder urothelial carcinoma sarcomatoid variant

disease
On this page

Also known as infiltrating bladder urothelial carcinoma, sarcomatoid variant with heterologous elementsinfiltrating bladder urothelial carcinoma, sarcomatoid variant without heterologous elementssarcomatoid carcinoma of the urinary bladder

Summary

Infiltrating bladder urothelial carcinoma sarcomatoid variant (MONDO:0004278) is a cancer and 3 clinical trials. Top therapeutic interventions include pemetrexed and vinblastine. A subtype of sarcomatoid transitional cell carcinoma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Classification: Cancer
  • Clinical trials: 3

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameinfiltrating bladder urothelial carcinoma sarcomatoid variant
Mondo IDMONDO:0004278
EFOEFO:1000303
DOIDDOID:7553
NCITC39824
UMLSC1512743
MedGen268929
GARD0023907
Anatomy (UBERON)UBERON:0001255
Is cancer (heuristic)yes

Also known as: infiltrating bladder urothelial carcinoma sarcomatoid variant · infiltrating bladder urothelial carcinoma, sarcomatoid variant with heterologous elements · infiltrating bladder urothelial carcinoma, sarcomatoid variant without heterologous elements · sarcomatoid carcinoma of the urinary bladder

Disease family

Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumorneoplastic disease or syndromeneoplasmcancercarcinomasarcomatoid carcinoma › sarcomatoid transitional cell carcinoma › infiltrating bladder urothelial carcinoma sarcomatoid variant

Related subtypes (2): kidney pelvis sarcomatoid transitional cell carcinoma, bladder sarcomatoid transitional cell 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: 3.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE22
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03744793PHASE2ACTIVE_NOT_RECRUITINGPemetrexed and Avelumab in Treating Patients With MTAP-Deficient Metastatic Urothelial Cancer
NCT03912818PHASE2TERMINATEDDurvalumab and Standard Chemotherapy Before Surgery in Treating Patients With Variant Histology Bladder Cancer
NCT02812420EARLY_PHASE1ACTIVE_NOT_RECRUITINGDurvalumab and Tremelimumab in Treating Patients With Muscle-Invasive, High-Risk Urothelial Cancer That Cannot Be Treated With Cisplatin-Based Therapy Before Surgery

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
PEMETREXED41
VINBLASTINE41
CHEMBL478849401