Fallopian tube endometrioid tumor

disease
On this page

Also known as endometrium neoplasm of fallopian tubefallopian tube endometrioid neoplasmfallopian tube endometrium neoplasm

Summary

Fallopian tube endometrioid tumor (MONDO:0021576) is a cancer and 4 clinical trials. Top therapeutic interventions include tremelimumab. A subtype of fallopian tube neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Classification: Cancer
  • Clinical trials: 4

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namefallopian tube endometrioid tumor
Mondo IDMONDO:0021576
NCITC40111
UMLSC1517113
MedGen274486
Anatomy (UBERON)UBERON:0003889
Is cancer (heuristic)yes

Also known as: endometrium neoplasm of fallopian tube · fallopian tube endometrioid neoplasm · fallopian tube endometrioid tumor · fallopian tube endometrium neoplasm

Disease family

This is a subtype of fallopian tube neoplasm. 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 › reproductive system disorderfemale reproductive system disorderfallopian tube disorderfallopian tube neoplasmfallopian tube endometrioid tumor

Related subtypes (4): fallopian tube benign neoplasm, fallopian tube cancer, fallopian tube mucinous tumor, fallopian tube germ cell tumor

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: 4.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE22
PHASE31
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT04575935PHASE3RECRUITINGMinimally Invasive Surgery After Neoadjuvant Chemotherapy for the Treatment of Stage IIIC-IV Ovarian, Primary Peritoneal, or Fallopian Tube Cancer, LANCE Trial
NCT04034927PHASE2ACTIVE_NOT_RECRUITINGTesting the Addition of an Immunotherapy Drug, Tremelimumab, to the PARP Inhibition Drug, Olaparib, for Recurrent Ovarian, Fallopian Tube or Peritoneal Cancer
NCT03685695PHASE2COMPLETEDPhysical Activity Monitored by Fitbit Charge 2 in Improving Quality of Life in Participants With Recurrent Ovarian, Primary Peritoneal, or Fallopian Tube Cancer
NCT02111941EARLY_PHASE1COMPLETEDVaccine Therapy for Patients With Stage IIIC-IV Ovarian Epithelial, Fallopian Tube, or Primary Peritoneal Cavity Cancer

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
TREMELIMUMAB41