Endometrium adenocarcinoma
diseaseOn this page
Also known as adenocarcinoma of endometriumadenocarcinoma of the endometriumadenocarcinoma, endometrial, malignantendometrial adenocarcinomaendometrioid adenoma or carcinoma NOS (morphologic abnormality)endometrioid adenomas and carcinomas (morphologic abnormality)endometrioid carcinoma of endometrium
Summary
Endometrium adenocarcinoma (MONDO:0005461) is a disease (an umbrella term covering 9 Mondo subtypes) with 2 cohort genes and 61 clinical trials. Molecularly, MTOR S2215Y confers sensitivity to Sirolimus in Endometrial Adenocarcinoma (CIViC Level D); 1 further subtype–drug associations are mapped below. Top therapeutic interventions include capivasertib, ixabepilone, and megestrol acetate.
At a glance
- Umbrella term: 9 Mondo subtypes
- Cohort genes: 2
- Clinical trials: 61
- Precision-medicine evidence (CIViC): 2 subtype–drug associations
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | endometrium adenocarcinoma |
| Mondo ID | MONDO:0005461 |
| EFO | EFO:0005232 |
| DOID | DOID:2870 |
| NCIT | C7359 |
| UMLS | C1153706 |
| MedGen | 218862 |
| Anatomy (UBERON) | UBERON:0001295 |
| Is cancer (heuristic) | no |
Also known as: adenocarcinoma of endometrium · adenocarcinoma of the endometrium · adenocarcinoma, endometrial, malignant · endometrial adenocarcinoma · endometrioid adenoma or carcinoma NOS (morphologic abnormality) · endometrioid adenomas and carcinomas (morphologic abnormality) · endometrioid carcinoma of endometrium · endometrium adenocarcinoma
Data availability: 65 cell lines.
Disease family
An umbrella term covering 9 Mondo subtypes.
Classification path: disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › cancer › reproductive system cancer › female reproductive organ cancer › uterine cancer › uterine carcinoma › endometrial carcinoma › endometrium adenocarcinoma
Related subtypes (6): uterine corpus endometrial carcinoma, endometrial transitional cell carcinoma, endometrium carcinoma in situ, endometrial small cell carcinoma, endometrial squamous cell carcinoma, endometrial undifferentiated carcinoma
Subtypes (9): endometrial mucinous adenocarcinoma, villoglandular endometrial endometrioid adenocarcinoma, oxyphilic endometrial endometrioid adenocarcinoma, secretory uterine corpus endometrioid adenocarcinoma, mucin-rich endometrial endometrioid adenocarcinoma, endometrial endometrioid adenocarcinoma with spindled epithelial cells, endometrial mixed adenocarcinoma, endometrial clear cell adenocarcinoma, ovarian endometrioid adenocarcinoma
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
Mendelian disease overlap and somatic drivers
GenCC: 0 · Orphanet: 24 · OMIM-shared: 0 · Dual-evidence (GWAS+Mendelian): 0
Orphanet rare-disease linkage (cohort genes)
| Gene | Orphanet ID | Rare disease |
|---|---|---|
| TP53 | Orphanet:1333 | Familial pancreatic carcinoma |
| TP53 | Orphanet:145 | Hereditary breast and/or ovarian cancer syndrome |
| TP53 | Orphanet:1501 | Adrenocortical carcinoma |
| TP53 | Orphanet:210159 | Adult hepatocellular carcinoma |
| TP53 | Orphanet:251576 | Gliosarcoma |
| TP53 | Orphanet:251579 | Giant cell glioblastoma |
| TP53 | Orphanet:251899 | Choroid plexus carcinoma |
| TP53 | Orphanet:2807 | Papilloma of choroid plexus |
| TP53 | Orphanet:293199 | Pleomorphic rhabdomyosarcoma |
| TP53 | Orphanet:3318 | Essential thrombocythemia |
| TP53 | Orphanet:524 | Li-Fraumeni syndrome |
| TP53 | Orphanet:52688 | Myelodysplastic syndrome |
| TP53 | Orphanet:585909 | B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2) |
| TP53 | Orphanet:667662 | Breast implant-associated anaplastic large cell lymphoma |
| TP53 | Orphanet:668 | Osteosarcoma |
| TP53 | Orphanet:67038 | B-cell chronic lymphocytic leukemia |
| TP53 | Orphanet:70573 | Small cell lung cancer |
| TP53 | Orphanet:96253 | Cushing disease |
| TP53 | Orphanet:99756 | Alveolar rhabdomyosarcoma |
| TP53 | Orphanet:99757 | Embryonal rhabdomyosarcoma |
| MTOR | Orphanet:269001 | Isolated focal cortical dysplasia type IIa |
| MTOR | Orphanet:269008 | Isolated focal cortical dysplasia type IIb |
| MTOR | Orphanet:457485 | Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome |
| MTOR | Orphanet:99802 | Hemimegalencephaly |
Cohort genes → proteins
2 cohort genes, 2 distinct canonical proteins.
Evidence partition
| Subset | Genes |
|---|---|
| civic_only | 2 |
Cohort genes (full)
| Symbol | HGNC | Ensembl | UniProt | Name | Evidence |
|---|---|---|---|---|---|
| TP53 | HGNC:11998 | ENSG00000141510 | P04637 | Cellular tumor antigen p53 | civic_evidence |
| MTOR | HGNC:3942 | ENSG00000198793 | P42345 | Serine/threonine-protein kinase mTOR | civic_evidence |
Cohort function summary
Lead sentence per gene, UniProt-curated.
| Symbol | Protein name | Function (lead sentence) |
|---|---|---|
| TP53 | Cellular tumor antigen p53 | Multifunctional transcription factor that induces cell cycle arrest, DNA repair or apoptosis upon binding to its target DNA sequence. |
| MTOR | Serine/threonine-protein kinase mTOR | Serine/threonine protein kinase which is a central regulator of cellular metabolism, growth and survival in response to hormones, growth factors, nutrients, energy and stress signals. |
Protein-family classification
Druggable: 1 · Difficult: 1 · Unknown: 0 · Druggable fraction: 0.5
Family distribution
Cohort families vs a genome-wide background (hypergeometric, BH-FDR; fold = observed/expected). Counts kept; sorted by enrichment, so the catch-all Other/Unknown bucket no longer leads.
| Family | Genes | Fold | FDR |
|---|---|---|---|
| Kinase | 1 | 13.9× | 0.142 |
| Transcription factor | 1 | 4.1× | 0.228 |
Per-gene assignment
| Symbol | Family | Druggable? | EC | InterPro (top 3) |
|---|---|---|---|---|
| TP53 | Transcription factor | no | p53_tumour_suppressor, p53-like_TF_DNA-bd_sf, p53_tetrameristn | |
| MTOR | Kinase | yes | PI3/4_kinase_cat_dom, PIK-rel_kinase_FAT, FATC_dom |
Expression context
Cohort genes with no expression data: 0.
2 cohort genes are a single-cell marker in ≥1 SCXA experiment.
Breadth distribution (Bgee present_calls)
| Bucket | Genes |
|---|---|
| narrow (1-5 tissues) | 0 |
| moderate (6-20) | 0 |
| broad (>20) | 2 |
| unknown | 0 |
Top tissues across cohort
| Tissue | Cohort genes |
|---|---|
| ganglionic eminence | 1 |
| tendon of biceps brachii | 1 |
| ventricular zone | 1 |
| cerebellar hemisphere | 1 |
| primordial germ cell in gonad | 1 |
| right hemisphere of cerebellum | 1 |
Per-gene tissue summary (top 30)
| Symbol | Bgee breadth | FANTOM5 breadth | SCXA | Top tissues |
|---|---|---|---|---|
| TP53 | 223 | ubiquitous | marker | ventricular zone, ganglionic eminence, tendon of biceps brachii |
| MTOR | 207 | ubiquitous | marker | primordial germ cell in gonad, right hemisphere of cerebellum, cerebellar hemisphere |
Protein interactions among cohort
Intra-cohort edges: 0.
Hub genes (top 10 by interactor count)
| Symbol | Interactor count |
|---|---|
| TP53 | 22,736 |
| MTOR | 9,490 |
Structural data
PDB: 2 · AlphaFold-only: 0 · No structure: 0
Cohort genes with PDB structures (top 30)
| Symbol | UniProt | PDB entries |
|---|---|---|
| TP53 | P04637 | 313 |
| MTOR | P42345 | 70 |
Function
Pathway analysis
Distinct Reactome pathways touched by cohort: 84. Enrichment computed across 2 evidence-associated genes (2 with Reactome annotation).
Pathways by enrichment
Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 2 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.
| Pathway | Cohort genes | Fold | FDR | Sample cohort genes |
|---|---|---|---|---|
| Regulation of TP53 Degradation | 2 | 292.8× | 1e-03 | TP53, MTOR |
| Regulation of PTEN gene transcription | 2 | 178.4× | 0.001 | TP53, MTOR |
| TP53 Regulates Metabolic Genes | 2 | 129.8× | 0.002 | TP53, MTOR |
| Loss of function of TP53 in cancer due to loss of tetramerization ability | 1 | 5710.0× | 0.004 | TP53 |
| Regulation of TP53 Expression | 1 | 2855.0× | 0.006 | TP53 |
| Transcriptional activation of cell cycle inhibitor p21 | 1 | 1427.5× | 0.010 | TP53 |
| Activation of NOXA and translocation to mitochondria | 1 | 951.7× | 0.012 | TP53 |
| RUNX3 regulates CDKN1A transcription | 1 | 815.7× | 0.012 | TP53 |
| PI5P Regulates TP53 Acetylation | 1 | 634.4× | 0.012 | TP53 |
| Activation of PUMA and translocation to mitochondria | 1 | 571.0× | 0.012 | TP53 |
| TP53 Regulates Transcription of Caspase Activators and Caspases | 1 | 475.8× | 0.012 | TP53 |
| TP53 Regulates Transcription of Death Receptors and Ligands | 1 | 475.8× | 0.012 | TP53 |
| Urea cycle | 1 | 439.2× | 0.012 | TP53 |
| Regulation of TP53 Activity through Association with Co-factors | 1 | 407.9× | 0.012 | TP53 |
| TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain | 1 | 380.7× | 0.012 | TP53 |
| Stabilization of p53 | 1 | 380.7× | 0.012 | TP53 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 1 | 356.9× | 0.012 | TP53 |
| Dengue virus modulates apoptosis | 1 | 356.9× | 0.012 | MTOR |
| Formation of Senescence-Associated Heterochromatin Foci (SAHF) | 1 | 335.9× | 0.012 | TP53 |
| Zygotic genome activation (ZGA) | 1 | 335.9× | 0.012 | TP53 |
| Regulation of NF-kappa B signaling | 1 | 317.2× | 0.012 | TP53 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 1 | 300.5× | 0.012 | TP53 |
| SUMOylation of transcription factors | 1 | 285.5× | 0.012 | TP53 |
| TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 1 | 271.9× | 0.012 | TP53 |
| Regulation of TP53 Activity through Methylation | 1 | 271.9× | 0.012 | TP53 |
| TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | 1 | 259.6× | 0.012 | TP53 |
| Regulation of TP53 Expression and Degradation | 1 | 259.6× | 0.012 | MTOR |
| mTORC1-mediated signalling | 1 | 237.9× | 0.012 | MTOR |
| Regulation of TP53 Activity through Acetylation | 1 | 228.4× | 0.012 | TP53 |
| Regulation of T cell activation by CD28 family | 1 | 211.5× | 0.012 | MTOR |
GO biological processes by enrichment
Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 2 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.
| GO term | Cohort genes | Fold | FDR | Sample cohort genes |
|---|---|---|---|---|
| negative regulation of helicase activity | 1 | 8426.0× | 0.003 | TP53 |
| positive regulation of SCF-dependent proteasomal ubiquitin-dependent catabolic process | 1 | 8426.0× | 0.003 | MTOR |
| cellular response to actinomycin D | 1 | 8426.0× | 0.003 | TP53 |
| regulation of intrinsic apoptotic signaling pathway by p53 class mediator | 1 | 8426.0× | 0.003 | TP53 |
| negative regulation of G1 to G0 transition | 1 | 8426.0× | 0.003 | TP53 |
| positive regulation of mitochondrial membrane permeability | 1 | 4213.0× | 0.003 | TP53 |
| oligodendrocyte apoptotic process | 1 | 4213.0× | 0.003 | TP53 |
| negative regulation of glucose catabolic process to lactate via pyruvate | 1 | 4213.0× | 0.003 | TP53 |
| regulation of locomotor rhythm | 1 | 4213.0× | 0.003 | MTOR |
| positive regulation of cytoplasmic translational initiation | 1 | 4213.0× | 0.003 | MTOR |
| negative regulation of pentose-phosphate shunt | 1 | 4213.0× | 0.003 | TP53 |
| multicellular organism growth | 2 | 137.0× | 0.003 | TP53, MTOR |
| cellular response to hypoxia | 2 | 121.2× | 0.003 | TP53, MTOR |
| protein stabilization | 2 | 66.9× | 0.003 | TP53, MTOR |
| obsolete homolactic fermentation | 1 | 2808.7× | 0.003 | TP53 |
| signal transduction by p53 class mediator | 1 | 2808.7× | 0.003 | TP53 |
| negative regulation of miRNA processing | 1 | 2808.7× | 0.003 | TP53 |
| intrinsic apoptotic signaling pathway in response to hypoxia | 1 | 2808.7× | 0.003 | TP53 |
| regulation of fibroblast apoptotic process | 1 | 2808.7× | 0.003 | TP53 |
| T-helper 1 cell lineage commitment | 1 | 2106.5× | 0.003 | MTOR |
| T cell proliferation involved in immune response | 1 | 2106.5× | 0.003 | TP53 |
| positive regulation of programmed necrotic cell death | 1 | 2106.5× | 0.003 | TP53 |
| oxidative stress-induced premature senescence | 1 | 2106.5× | 0.003 | TP53 |
| negative regulation of lysosome organization | 1 | 2106.5× | 0.003 | MTOR |
| positive regulation of pentose-phosphate shunt | 1 | 2106.5× | 0.003 | MTOR |
| B cell lineage commitment | 1 | 1685.2× | 0.003 | TP53 |
| T cell lineage commitment | 1 | 1685.2× | 0.003 | TP53 |
| mRNA transcription | 1 | 1685.2× | 0.003 | TP53 |
| positive regulation of RNA polymerase II transcription preinitiation complex assembly | 1 | 1685.2× | 0.003 | TP53 |
| cellular response to methionine | 1 | 1685.2× | 0.003 | MTOR |
Therapeutics
Drug target analysis
Approved (phase 4): 2 · Phase ≥3: 2 · Phased (≥1): 2 · Undrugged: 0
Druggability breadth: 2 of 2 evidence-associated genes (100%) have a ChEMBL target (buckets above are over the deeply-mined display cohort).
Genes with an approved drug
The molecule shown is one approved compound that hits the gene — not necessarily a drug of choice or one indicated for this disease.
| Symbol | Example approved molecule |
|---|---|
| TP53 | NITROFURANTOIN |
| MTOR | SALMETEROL XINAFOATE |
Top cohort targets by molecule count
| Symbol | Molecules | Max phase |
|---|---|---|
| TP53 | 196 | 4 |
| MTOR | 164 | 4 |
Drugs targeting cohort genes (top 30)
| Molecule | Max phase | Targets in cohort |
|---|---|---|
| NITROFURANTOIN | 4 | TP53 |
| DIOSMIN | 4 | TP53 |
| VERTEPORFIN | 4 | TP53 |
| CANDESARTAN CILEXETIL | 4 | TP53 |
| DIENESTROL | 4 | TP53 |
| CLOTRIMAZOLE | 4 | TP53 |
| COLCHICINE | 4 | TP53 |
| NABUMETONE | 4 | TP53 |
| SALMETEROL XINAFOATE | 4 | MTOR, TP53 |
| AMIODARONE HYDROCHLORIDE | 4 | TP53 |
| FURAZOLIDONE | 4 | TP53 |
| AMOXAPINE | 4 | MTOR, TP53 |
| RALOXIFENE HYDROCHLORIDE | 4 | TP53 |
| NICARDIPINE HYDROCHLORIDE | 4 | TP53 |
| SULCONAZOLE NITRATE | 4 | TP53 |
| PYRITHIONE ZINC | 4 | TP53 |
| LACTIC ACID | 4 | TP53 |
| OXYMETHOLONE | 4 | TP53 |
| CHLOROXINE | 4 | TP53 |
| PROPIOLACTONE | 4 | TP53 |
| CLOMIPRAMINE HYDROCHLORIDE | 4 | TP53 |
| PHENYL AMINOSALICYLATE | 4 | TP53 |
| THIORIDAZINE HYDROCHLORIDE | 4 | TP53 |
| AMITRIPTYLINE HYDROCHLORIDE | 4 | TP53 |
| ETHOPROPAZINE HYDROCHLORIDE | 4 | TP53 |
| MECHLORETHAMINE HYDROCHLORIDE | 4 | TP53 |
| ECONAZOLE NITRATE | 4 | TP53 |
| TRIFLUPROMAZINE HYDROCHLORIDE | 4 | TP53 |
| PROCHLORPERAZINE EDISYLATE | 4 | TP53 |
| DEQUALINIUM CHLORIDE | 4 | TP53 |
Bioactivity and enzyme data
Enzyme cohort genes (≥1 EC): 0.
Cohort genes with ChEMBL bioactivity (full, sorted by assay count)
| Symbol | Assays | Type breakdown |
|---|---|---|
| MTOR | 1,375 | Binding:1335, Functional:37, ADMET:2, Toxicity:1 |
| TP53 | 869 | Binding:775, ADMET:83, Functional:10, Toxicity:1 |
Cohort genes with high screening signal
≥100 ChEMBL assays — a studied-ness signal; see Therapeutics for approved-drug status.
| Symbol | ChEMBL assays |
|---|---|
| TP53 | 869 |
| MTOR | 1,375 |
Pharmacogenomics
Cohort genes with a PharmGKB record: 2; with CPIC/DPWG dosing guidelines: 0.
No cohort gene has a CPIC/DPWG genotype-guided dosing guideline (PharmGKB).
Chemical tractability of cohort targets
30 approved/phased compounds have measured bioactivity against a cohort gene (and aren’t yet in disease-level trials). This is a research / tractability signal, NOT a therapeutic recommendation — a bioactivity row often reflects off-target or screening binding (e.g. promiscuous kinase inhibitors against a cohort kinase), implying no disease mechanism.
| Compound | Max phase | Cohort target (bioactivity) |
|---|---|---|
| NITROFURANTOIN | 4 | TP53 |
| DIOSMIN | 4 | TP53 |
| VERTEPORFIN | 4 | TP53 |
| CANDESARTAN CILEXETIL | 4 | TP53 |
| DIENESTROL | 4 | TP53 |
| CLOTRIMAZOLE | 4 | TP53 |
| COLCHICINE | 4 | TP53 |
| NABUMETONE | 4 | TP53 |
| SALMETEROL XINAFOATE | 4 | MTOR, TP53 |
| AMIODARONE HYDROCHLORIDE | 4 | TP53 |
| FURAZOLIDONE | 4 | TP53 |
| AMOXAPINE | 4 | MTOR, TP53 |
| RALOXIFENE HYDROCHLORIDE | 4 | TP53 |
| NICARDIPINE HYDROCHLORIDE | 4 | TP53 |
| SULCONAZOLE NITRATE | 4 | TP53 |
| PYRITHIONE ZINC | 4 | TP53 |
| LACTIC ACID | 4 | TP53 |
| OXYMETHOLONE | 4 | TP53 |
| CHLOROXINE | 4 | TP53 |
| PROPIOLACTONE | 4 | TP53 |
| CLOMIPRAMINE HYDROCHLORIDE | 4 | TP53 |
| PHENYL AMINOSALICYLATE | 4 | TP53 |
| THIORIDAZINE HYDROCHLORIDE | 4 | TP53 |
| AMITRIPTYLINE HYDROCHLORIDE | 4 | TP53 |
| ETHOPROPAZINE HYDROCHLORIDE | 4 | TP53 |
| MECHLORETHAMINE HYDROCHLORIDE | 4 | TP53 |
| ECONAZOLE NITRATE | 4 | TP53 |
| TRIFLUPROMAZINE HYDROCHLORIDE | 4 | TP53 |
| PROCHLORPERAZINE EDISYLATE | 4 | TP53 |
| DEQUALINIUM CHLORIDE | 4 | TP53 |
Druggability pyramid
Cohort genes binned by druggability tier (high → low):
| Tier | Definition | Genes | Symbols |
|---|---|---|---|
| A | Approved (phase 4 drug) | 2 | TP53, MTOR |
| B | Phased (≥1) drug, not yet approved | 0 | |
| C | Druggable family + PDB, no drug | 0 | |
| D | Druggable family + AlphaFold only, no drug | 0 | |
| E | Difficult family or no structure, no drug | 0 |
Undrugged target profiles
0 cohort genes are undrugged. Ranked by ‘starting-point quality’ (assay depth + drugged-partner adjacency).
Clinical trials & evidence
Clinical trials
Clinical trials: 61.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| PHASE2 | 32 |
| Not specified | 12 |
| PHASE1 | 9 |
| PHASE3 | 3 |
| PHASE1/PHASE2 | 3 |
| PHASE4 | 1 |
| PHASE2/PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT03164590 | PHASE4 | COMPLETED | Effects of Wound Infiltration With Ketamine Versus Dexmedetomidine Added to Bupivacaine on Cytokines |
| NCT03914612 | PHASE3 | ACTIVE_NOT_RECRUITING | Testing the Addition of the Immunotherapy Drug Pembrolizumab to the Usual Chemotherapy Treatment (Paclitaxel and Carboplatin) in Stage III-IV or Recurrent Endometrial Cancer |
| NCT00002706 | PHASE3 | COMPLETED | Laparoscopic Surgery or Standard Surgery in Treating Patients With Endometrial Cancer or Cancer of the Uterus |
| NCT00006011 | PHASE3 | COMPLETED | Comparison of Two Combination Chemotherapy Regimens Plus Radiation Therapy in Treating Patients With Stage III or Stage IV Endometrial Cancer |
| NCT02065687 | PHASE2/PHASE3 | UNKNOWN | Paclitaxel and Carboplatin With or Without Metformin Hydrochloride in Treating Patients With Stage III, IV, or Recurrent Endometrial Cancer |
| NCT00977574 | PHASE2 | ACTIVE_NOT_RECRUITING | Paclitaxel, Carboplatin, and Bevacizumab or Paclitaxel, Carboplatin, and Temsirolimus or Ixabepilone, Carboplatin, and Bevacizumab in Treating Patients With Stage III, Stage IV, or Recurrent Endometrial Cancer |
| NCT03660826 | PHASE2 | ACTIVE_NOT_RECRUITING | Testing the Combination of Olaparib and Durvalumab, Cediranib and Durvalumab, Olaparib and Capivasertib, and Cediranib Alone in Recurrent or Refractory Endometrial Cancer Following the Earlier Phase of the Study That Tested Olaparib and Cediranib in Comparison to Cediranib Alone, and Olaparib Alone |
| NCT04106414 | PHASE2 | ACTIVE_NOT_RECRUITING | Study of BMS-986205 and Nivolumab in Endometrial Cancer or Endometrial Carcinosarcoma That Has Not Responded to Treatment |
| NCT04719273 | PHASE2 | ACTIVE_NOT_RECRUITING | Onapristone and Anastrozole for the Treatment of Refractory Hormone Receptor Positive Endometrial Cancer |
| NCT05112601 | PHASE2 | RECRUITING | Testing Nivolumab With or Without Ipilimumab in Deficient Mismatch Repair System (dMMR) Recurrent Endometrial Carcinoma |
| NCT05548296 | PHASE2 | RECRUITING | A Phase 2 Study of ACR-368 in Endometrial Adenocarcinoma |
| NCT05824481 | PHASE2 | ACTIVE_NOT_RECRUITING | Study of Cadonilimab (AK104) Plus Lenvatinib in Patients With Advanced Endometrial Cancer |
| NCT06066216 | PHASE2 | NOT_YET_RECRUITING | Cadonilimab (AK104) Plus Chemotherapy in Patients With Recurrent or Advanced Endometrial Cancer |
| NCT06399757 | PHASE1/PHASE2 | RECRUITING | A Study to Investigate APL-5125 in Adults With Advanced Solid Tumors |
| NCT06917092 | PHASE2 | RECRUITING | QL1706-Based Therapy Post-PD-1/L1 Failure in Advanced Endometrial Cancer |
| NCT00006089 | PHASE2 | COMPLETED | Trastuzumab in Treating Patients With Stage III, Stage IV, or Recurrent Endometrial Cancer |
| NCT00025467 | PHASE2 | COMPLETED | Thalidomide in Treating Patients With Recurrent or Persistent Endometrial Cancer |
| NCT00064025 | PHASE2 | COMPLETED | Medroxyprogesterone in Treating Patients With Endometrioid Adenocarcinoma of the Uterine Corpus |
| NCT00072176 | PHASE2 | COMPLETED | Temsirolimus in Treating Patients With Metastatic or Locally Advanced Recurrent Endometrial Cancer |
| NCT00095979 | PHASE2 | COMPLETED | Ixabepilone in Treating Patients With Recurrent or Persistent Endometrial Cancer |
| NCT00478426 | PHASE2 | COMPLETED | Sunitinib Malate in Treating Patients With Recurrent or Metastatic Endometrial Cancer |
| NCT00820898 | PHASE2 | COMPLETED | Gemcitabine in Treating Patients With Recurrent or Persistent Endometrial Cancer |
| NCT00888173 | PHASE2 | COMPLETED | Brivanib Alaninate in Treating Patients With Recurrent or Persistent Endometrial Cancer |
| NCT01005329 | PHASE2 | COMPLETED | Intensity-Modulated Radiation Therapy, Cisplatin, and Bevacizumab Followed by Carboplatin and Paclitaxel in Treating Patients Who Have Undergone Surgery for Endometrial Cancer |
| NCT01011933 | PHASE2 | COMPLETED | Selumetinib in Treating Patients With Recurrent or Persistent Endometrial Cancer |
| NCT01041027 | PHASE2 | TERMINATED | Radiation Therapy, Paclitaxel, and Carboplatin in Treating Patients With High-Risk Endometrial Cancer |
| NCT01132820 | PHASE2 | COMPLETED | Cediranib Maleate in Treating Patients With Recurrent or Persistent Endometrial Cancer |
| NCT01210222 | PHASE2 | COMPLETED | Trebananib in Treating Patients With Persistent or Recurrent Endometrial Cancer |
| NCT01225887 | PHASE2 | COMPLETED | Nintedanib in Treating Patients With Recurrent or Persistent Endometrial Cancer |
| NCT01307631 | PHASE2 | COMPLETED | Akt Inhibitor MK2206 in Treating Patients With Recurrent or Advanced Endometrial Cancer |
| NCT01642082 | PHASE2 | COMPLETED | Dalantercept in Treating Patients With Recurrent or Persistent Endometrial Cancer |
| NCT01877564 | PHASE2 | COMPLETED | A Randomized Pilot Study to Evaluate the Effects of a Short Course of Metformin Versus No Therapy in the Period Prior to Hysterectomy for Grade 1-2 Adenocarcinoma of the Endometrium in Obese Non-Diabetic Women |
| NCT01943058 | PHASE2 | WITHDRAWN | Megestrol Acetate or Levonorgestrel-Releasing Intrauterine System in Treating Patients With Atypical Endometrial Hyperplasia or Endometrial Cancer |
| NCT01968317 | PHASE2 | COMPLETED | Megestrol Acetate Plus Metformin to Megestrol Acetate in Patients With Endometrial Atypical Hyperplasia or Early Stage Endometrial Adenocarcinoma |
| NCT02549209 | PHASE2 | COMPLETED | Pembro/Carbo/Taxol in Endometrial Cancer |
| NCT03221400 | PHASE1/PHASE2 | UNKNOWN | PEN-866 in Patients With Advanced Solid Malignancies |
| NCT03540407 | PHASE2 | COMPLETED | Evaluation of Oncoxin-Viusid® in Cervical Cancer and Endometrial Adenocarcinoma. |
| NCT03643510 | PHASE2 | COMPLETED | Evaluating Cancer Response to Treatment With Abemaciclib and Fulvestrant in Women With Recurrent Endometrial Cancer |
| NCT03836157 | PHASE2 | WITHDRAWN | Mirvetuximab Soravtansine (IMGN853) and Bevacizumab in Patients With Endometrial Cancer |
| NCT05001282 | PHASE1/PHASE2 | TERMINATED | A Study to Evaluate ELU001 in Patients With Solid Tumors That Overexpress Folate Receptor Alpha (FRα) |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| CAPIVASERTIB | 4 | 2 |
| IXABEPILONE | 4 | 2 |
| MEGESTROL ACETATE | 4 | 2 |
| TEMSIROLIMUS | 4 | 2 |
| ABEMACICLIB | 4 | 1 |
| BUPIVACAINE | 4 | 1 |
| COPANLISIB | 4 | 1 |
| DURVALUMAB | 4 | 1 |
| FILGRASTIM | 4 | 1 |
| LURBINECTEDIN | 4 | 1 |
| MEDROXYPROGESTERONE ACETATE | 4 | 1 |
| METFORMIN | 4 | 1 |
| MIRVETUXIMAB SORAVTANSINE | 4 | 1 |
| NINTEDANIB | 4 | 1 |
| NIRAPARIB | 4 | 1 |
| PACLITAXEL | 4 | 1 |
| PEGFILGRASTIM | 4 | 1 |
| PEMBROLIZUMAB | 4 | 1 |
| RUXOLITINIB PHOSPHATE | 4 | 1 |
| SELUMETINIB | 4 | 1 |
| SODIUM PERTECHNETATE TC 99M | 4 | 1 |
| SUNITINIB MALATE | 4 | 1 |
| CADONILIMAB | 3 | 2 |
| CEDIRANIB MALEATE | 3 | 2 |
| BRIVANIB ALANINATE | 3 | 1 |
| DALANTERCEPT | 3 | 1 |
| TREBANANIB | 3 | 1 |
| ONAPRISTONE | 2 | 1 |
| UPROSERTIB | 2 | 1 |
| VISTUSERTIB | 2 | 1 |
Precision-medicine subtype map (CIViC)
Drug × molecular subtype: 2 predictive associations from 2 curated evidence items; also 1 oncogenic.
| Molecular subtype | Therapy | Effect | Level | CIViC |
|---|---|---|---|---|
| MTOR S2215Y | Sirolimus | Sensitivity/Response | CIViC D | EID1319 |
| TP53 R175H | MDM2 Inhibitor AMGMDS3 | Resistance | CIViC D | EID10076 |
Related Atlas pages
- Cohort genes: TP53, MTOR
- Drugs: Capivasertib, Ixabepilone, Megestrol Acetate, Temsirolimus, Abemaciclib, Bupivacaine, Copanlisib, Durvalumab, Filgrastim, Lurbinectedin, Medroxyprogesterone Acetate, Metformin, Mirvetuximab Soravtansine, Nintedanib, Niraparib, Paclitaxel, Pegfilgrastim, Pembrolizumab, Ruxolitinib Phosphate, Selumetinib, SODIUM PERTECHNETATE TC 99M, Sunitinib Malate, Cadonilimab, Cediranib, Brivanib Alaninate, Dalantercept, Trebananib, Sirolimus