Endometrium adenocarcinoma

disease
On 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

FieldValue
Canonical nameendometrium adenocarcinoma
Mondo IDMONDO:0005461
EFOEFO:0005232
DOIDDOID:2870
NCITC7359
UMLSC1153706
MedGen218862
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 tumorneoplastic disease or syndromeneoplasmcancerreproductive system cancerfemale reproductive organ canceruterine canceruterine carcinomaendometrial carcinomaendometrium 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)

GeneOrphanet IDRare disease
TP53Orphanet:1333Familial pancreatic carcinoma
TP53Orphanet:145Hereditary breast and/or ovarian cancer syndrome
TP53Orphanet:1501Adrenocortical carcinoma
TP53Orphanet:210159Adult hepatocellular carcinoma
TP53Orphanet:251576Gliosarcoma
TP53Orphanet:251579Giant cell glioblastoma
TP53Orphanet:251899Choroid plexus carcinoma
TP53Orphanet:2807Papilloma of choroid plexus
TP53Orphanet:293199Pleomorphic rhabdomyosarcoma
TP53Orphanet:3318Essential thrombocythemia
TP53Orphanet:524Li-Fraumeni syndrome
TP53Orphanet:52688Myelodysplastic syndrome
TP53Orphanet:585909B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)
TP53Orphanet:667662Breast implant-associated anaplastic large cell lymphoma
TP53Orphanet:668Osteosarcoma
TP53Orphanet:67038B-cell chronic lymphocytic leukemia
TP53Orphanet:70573Small cell lung cancer
TP53Orphanet:96253Cushing disease
TP53Orphanet:99756Alveolar rhabdomyosarcoma
TP53Orphanet:99757Embryonal rhabdomyosarcoma
MTOROrphanet:269001Isolated focal cortical dysplasia type IIa
MTOROrphanet:269008Isolated focal cortical dysplasia type IIb
MTOROrphanet:457485Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome
MTOROrphanet:99802Hemimegalencephaly

Cohort genes → proteins

2 cohort genes, 2 distinct canonical proteins.

Evidence partition

SubsetGenes
civic_only2

Cohort genes (full)

SymbolHGNCEnsemblUniProtNameEvidence
TP53HGNC:11998ENSG00000141510P04637Cellular tumor antigen p53civic_evidence
MTORHGNC:3942ENSG00000198793P42345Serine/threonine-protein kinase mTORcivic_evidence

Cohort function summary

Lead sentence per gene, UniProt-curated.

SymbolProtein nameFunction (lead sentence)
TP53Cellular tumor antigen p53Multifunctional transcription factor that induces cell cycle arrest, DNA repair or apoptosis upon binding to its target DNA sequence.
MTORSerine/threonine-protein kinase mTORSerine/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.

FamilyGenesFoldFDR
Kinase113.9×0.142
Transcription factor14.1×0.228

Per-gene assignment

SymbolFamilyDruggable?ECInterPro (top 3)
TP53Transcription factornop53_tumour_suppressor, p53-like_TF_DNA-bd_sf, p53_tetrameristn
MTORKinaseyesPI3/4_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)

BucketGenes
narrow (1-5 tissues)0
moderate (6-20)0
broad (>20)2
unknown0

Top tissues across cohort

TissueCohort genes
ganglionic eminence1
tendon of biceps brachii1
ventricular zone1
cerebellar hemisphere1
primordial germ cell in gonad1
right hemisphere of cerebellum1

Per-gene tissue summary (top 30)

SymbolBgee breadthFANTOM5 breadthSCXATop tissues
TP53223ubiquitousmarkerventricular zone, ganglionic eminence, tendon of biceps brachii
MTOR207ubiquitousmarkerprimordial 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)

SymbolInteractor count
TP5322,736
MTOR9,490

Structural data

PDB: 2 · AlphaFold-only: 0 · No structure: 0

Cohort genes with PDB structures (top 30)

SymbolUniProtPDB entries
TP53P04637313
MTORP4234570

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.

PathwayCohort genesFoldFDRSample cohort genes
Regulation of TP53 Degradation2292.8×1e-03TP53, MTOR
Regulation of PTEN gene transcription2178.4×0.001TP53, MTOR
TP53 Regulates Metabolic Genes2129.8×0.002TP53, MTOR
Loss of function of TP53 in cancer due to loss of tetramerization ability15710.0×0.004TP53
Regulation of TP53 Expression12855.0×0.006TP53
Transcriptional activation of cell cycle inhibitor p2111427.5×0.010TP53
Activation of NOXA and translocation to mitochondria1951.7×0.012TP53
RUNX3 regulates CDKN1A transcription1815.7×0.012TP53
PI5P Regulates TP53 Acetylation1634.4×0.012TP53
Activation of PUMA and translocation to mitochondria1571.0×0.012TP53
TP53 Regulates Transcription of Caspase Activators and Caspases1475.8×0.012TP53
TP53 Regulates Transcription of Death Receptors and Ligands1475.8×0.012TP53
Urea cycle1439.2×0.012TP53
Regulation of TP53 Activity through Association with Co-factors1407.9×0.012TP53
TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain1380.7×0.012TP53
Stabilization of p531380.7×0.012TP53
TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest1356.9×0.012TP53
Dengue virus modulates apoptosis1356.9×0.012MTOR
Formation of Senescence-Associated Heterochromatin Foci (SAHF)1335.9×0.012TP53
Zygotic genome activation (ZGA)1335.9×0.012TP53
Regulation of NF-kappa B signaling1317.2×0.012TP53
TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest1300.5×0.012TP53
SUMOylation of transcription factors1285.5×0.012TP53
TP53 Regulates Transcription of Genes Involved in Cytochrome C Release1271.9×0.012TP53
Regulation of TP53 Activity through Methylation1271.9×0.012TP53
TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain1259.6×0.012TP53
Regulation of TP53 Expression and Degradation1259.6×0.012MTOR
mTORC1-mediated signalling1237.9×0.012MTOR
Regulation of TP53 Activity through Acetylation1228.4×0.012TP53
Regulation of T cell activation by CD28 family1211.5×0.012MTOR

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 termCohort genesFoldFDRSample cohort genes
negative regulation of helicase activity18426.0×0.003TP53
positive regulation of SCF-dependent proteasomal ubiquitin-dependent catabolic process18426.0×0.003MTOR
cellular response to actinomycin D18426.0×0.003TP53
regulation of intrinsic apoptotic signaling pathway by p53 class mediator18426.0×0.003TP53
negative regulation of G1 to G0 transition18426.0×0.003TP53
positive regulation of mitochondrial membrane permeability14213.0×0.003TP53
oligodendrocyte apoptotic process14213.0×0.003TP53
negative regulation of glucose catabolic process to lactate via pyruvate14213.0×0.003TP53
regulation of locomotor rhythm14213.0×0.003MTOR
positive regulation of cytoplasmic translational initiation14213.0×0.003MTOR
negative regulation of pentose-phosphate shunt14213.0×0.003TP53
multicellular organism growth2137.0×0.003TP53, MTOR
cellular response to hypoxia2121.2×0.003TP53, MTOR
protein stabilization266.9×0.003TP53, MTOR
obsolete homolactic fermentation12808.7×0.003TP53
signal transduction by p53 class mediator12808.7×0.003TP53
negative regulation of miRNA processing12808.7×0.003TP53
intrinsic apoptotic signaling pathway in response to hypoxia12808.7×0.003TP53
regulation of fibroblast apoptotic process12808.7×0.003TP53
T-helper 1 cell lineage commitment12106.5×0.003MTOR
T cell proliferation involved in immune response12106.5×0.003TP53
positive regulation of programmed necrotic cell death12106.5×0.003TP53
oxidative stress-induced premature senescence12106.5×0.003TP53
negative regulation of lysosome organization12106.5×0.003MTOR
positive regulation of pentose-phosphate shunt12106.5×0.003MTOR
B cell lineage commitment11685.2×0.003TP53
T cell lineage commitment11685.2×0.003TP53
mRNA transcription11685.2×0.003TP53
positive regulation of RNA polymerase II transcription preinitiation complex assembly11685.2×0.003TP53
cellular response to methionine11685.2×0.003MTOR

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.

SymbolExample approved molecule
TP53NITROFURANTOIN
MTORSALMETEROL XINAFOATE

Top cohort targets by molecule count

SymbolMoleculesMax phase
TP531964
MTOR1644

Drugs targeting cohort genes (top 30)

MoleculeMax phaseTargets in cohort
NITROFURANTOIN4TP53
DIOSMIN4TP53
VERTEPORFIN4TP53
CANDESARTAN CILEXETIL4TP53
DIENESTROL4TP53
CLOTRIMAZOLE4TP53
COLCHICINE4TP53
NABUMETONE4TP53
SALMETEROL XINAFOATE4MTOR, TP53
AMIODARONE HYDROCHLORIDE4TP53
FURAZOLIDONE4TP53
AMOXAPINE4MTOR, TP53
RALOXIFENE HYDROCHLORIDE4TP53
NICARDIPINE HYDROCHLORIDE4TP53
SULCONAZOLE NITRATE4TP53
PYRITHIONE ZINC4TP53
LACTIC ACID4TP53
OXYMETHOLONE4TP53
CHLOROXINE4TP53
PROPIOLACTONE4TP53
CLOMIPRAMINE HYDROCHLORIDE4TP53
PHENYL AMINOSALICYLATE4TP53
THIORIDAZINE HYDROCHLORIDE4TP53
AMITRIPTYLINE HYDROCHLORIDE4TP53
ETHOPROPAZINE HYDROCHLORIDE4TP53
MECHLORETHAMINE HYDROCHLORIDE4TP53
ECONAZOLE NITRATE4TP53
TRIFLUPROMAZINE HYDROCHLORIDE4TP53
PROCHLORPERAZINE EDISYLATE4TP53
DEQUALINIUM CHLORIDE4TP53

Bioactivity and enzyme data

Enzyme cohort genes (≥1 EC): 0.

Cohort genes with ChEMBL bioactivity (full, sorted by assay count)

SymbolAssaysType breakdown
MTOR1,375Binding:1335, Functional:37, ADMET:2, Toxicity:1
TP53869Binding: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.

SymbolChEMBL assays
TP53869
MTOR1,375

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.

CompoundMax phaseCohort target (bioactivity)
NITROFURANTOIN4TP53
DIOSMIN4TP53
VERTEPORFIN4TP53
CANDESARTAN CILEXETIL4TP53
DIENESTROL4TP53
CLOTRIMAZOLE4TP53
COLCHICINE4TP53
NABUMETONE4TP53
SALMETEROL XINAFOATE4MTOR, TP53
AMIODARONE HYDROCHLORIDE4TP53
FURAZOLIDONE4TP53
AMOXAPINE4MTOR, TP53
RALOXIFENE HYDROCHLORIDE4TP53
NICARDIPINE HYDROCHLORIDE4TP53
SULCONAZOLE NITRATE4TP53
PYRITHIONE ZINC4TP53
LACTIC ACID4TP53
OXYMETHOLONE4TP53
CHLOROXINE4TP53
PROPIOLACTONE4TP53
CLOMIPRAMINE HYDROCHLORIDE4TP53
PHENYL AMINOSALICYLATE4TP53
THIORIDAZINE HYDROCHLORIDE4TP53
AMITRIPTYLINE HYDROCHLORIDE4TP53
ETHOPROPAZINE HYDROCHLORIDE4TP53
MECHLORETHAMINE HYDROCHLORIDE4TP53
ECONAZOLE NITRATE4TP53
TRIFLUPROMAZINE HYDROCHLORIDE4TP53
PROCHLORPERAZINE EDISYLATE4TP53
DEQUALINIUM CHLORIDE4TP53

Druggability pyramid

Cohort genes binned by druggability tier (high → low):

TierDefinitionGenesSymbols
AApproved (phase 4 drug)2TP53, MTOR
BPhased (≥1) drug, not yet approved0
CDruggable family + PDB, no drug0
DDruggable family + AlphaFold only, no drug0
EDifficult family or no structure, no drug0

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)

PhaseTrials
PHASE232
Not specified12
PHASE19
PHASE33
PHASE1/PHASE23
PHASE41
PHASE2/PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03164590PHASE4COMPLETEDEffects of Wound Infiltration With Ketamine Versus Dexmedetomidine Added to Bupivacaine on Cytokines
NCT03914612PHASE3ACTIVE_NOT_RECRUITINGTesting the Addition of the Immunotherapy Drug Pembrolizumab to the Usual Chemotherapy Treatment (Paclitaxel and Carboplatin) in Stage III-IV or Recurrent Endometrial Cancer
NCT00002706PHASE3COMPLETEDLaparoscopic Surgery or Standard Surgery in Treating Patients With Endometrial Cancer or Cancer of the Uterus
NCT00006011PHASE3COMPLETEDComparison of Two Combination Chemotherapy Regimens Plus Radiation Therapy in Treating Patients With Stage III or Stage IV Endometrial Cancer
NCT02065687PHASE2/PHASE3UNKNOWNPaclitaxel and Carboplatin With or Without Metformin Hydrochloride in Treating Patients With Stage III, IV, or Recurrent Endometrial Cancer
NCT00977574PHASE2ACTIVE_NOT_RECRUITINGPaclitaxel, 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
NCT03660826PHASE2ACTIVE_NOT_RECRUITINGTesting 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
NCT04106414PHASE2ACTIVE_NOT_RECRUITINGStudy of BMS-986205 and Nivolumab in Endometrial Cancer or Endometrial Carcinosarcoma That Has Not Responded to Treatment
NCT04719273PHASE2ACTIVE_NOT_RECRUITINGOnapristone and Anastrozole for the Treatment of Refractory Hormone Receptor Positive Endometrial Cancer
NCT05112601PHASE2RECRUITINGTesting Nivolumab With or Without Ipilimumab in Deficient Mismatch Repair System (dMMR) Recurrent Endometrial Carcinoma
NCT05548296PHASE2RECRUITINGA Phase 2 Study of ACR-368 in Endometrial Adenocarcinoma
NCT05824481PHASE2ACTIVE_NOT_RECRUITINGStudy of Cadonilimab (AK104) Plus Lenvatinib in Patients With Advanced Endometrial Cancer
NCT06066216PHASE2NOT_YET_RECRUITINGCadonilimab (AK104) Plus Chemotherapy in Patients With Recurrent or Advanced Endometrial Cancer
NCT06399757PHASE1/PHASE2RECRUITINGA Study to Investigate APL-5125 in Adults With Advanced Solid Tumors
NCT06917092PHASE2RECRUITINGQL1706-Based Therapy Post-PD-1/L1 Failure in Advanced Endometrial Cancer
NCT00006089PHASE2COMPLETEDTrastuzumab in Treating Patients With Stage III, Stage IV, or Recurrent Endometrial Cancer
NCT00025467PHASE2COMPLETEDThalidomide in Treating Patients With Recurrent or Persistent Endometrial Cancer
NCT00064025PHASE2COMPLETEDMedroxyprogesterone in Treating Patients With Endometrioid Adenocarcinoma of the Uterine Corpus
NCT00072176PHASE2COMPLETEDTemsirolimus in Treating Patients With Metastatic or Locally Advanced Recurrent Endometrial Cancer
NCT00095979PHASE2COMPLETEDIxabepilone in Treating Patients With Recurrent or Persistent Endometrial Cancer
NCT00478426PHASE2COMPLETEDSunitinib Malate in Treating Patients With Recurrent or Metastatic Endometrial Cancer
NCT00820898PHASE2COMPLETEDGemcitabine in Treating Patients With Recurrent or Persistent Endometrial Cancer
NCT00888173PHASE2COMPLETEDBrivanib Alaninate in Treating Patients With Recurrent or Persistent Endometrial Cancer
NCT01005329PHASE2COMPLETEDIntensity-Modulated Radiation Therapy, Cisplatin, and Bevacizumab Followed by Carboplatin and Paclitaxel in Treating Patients Who Have Undergone Surgery for Endometrial Cancer
NCT01011933PHASE2COMPLETEDSelumetinib in Treating Patients With Recurrent or Persistent Endometrial Cancer
NCT01041027PHASE2TERMINATEDRadiation Therapy, Paclitaxel, and Carboplatin in Treating Patients With High-Risk Endometrial Cancer
NCT01132820PHASE2COMPLETEDCediranib Maleate in Treating Patients With Recurrent or Persistent Endometrial Cancer
NCT01210222PHASE2COMPLETEDTrebananib in Treating Patients With Persistent or Recurrent Endometrial Cancer
NCT01225887PHASE2COMPLETEDNintedanib in Treating Patients With Recurrent or Persistent Endometrial Cancer
NCT01307631PHASE2COMPLETEDAkt Inhibitor MK2206 in Treating Patients With Recurrent or Advanced Endometrial Cancer
NCT01642082PHASE2COMPLETEDDalantercept in Treating Patients With Recurrent or Persistent Endometrial Cancer
NCT01877564PHASE2COMPLETEDA 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
NCT01943058PHASE2WITHDRAWNMegestrol Acetate or Levonorgestrel-Releasing Intrauterine System in Treating Patients With Atypical Endometrial Hyperplasia or Endometrial Cancer
NCT01968317PHASE2COMPLETEDMegestrol Acetate Plus Metformin to Megestrol Acetate in Patients With Endometrial Atypical Hyperplasia or Early Stage Endometrial Adenocarcinoma
NCT02549209PHASE2COMPLETEDPembro/Carbo/Taxol in Endometrial Cancer
NCT03221400PHASE1/PHASE2UNKNOWNPEN-866 in Patients With Advanced Solid Malignancies
NCT03540407PHASE2COMPLETEDEvaluation of Oncoxin-Viusid® in Cervical Cancer and Endometrial Adenocarcinoma.
NCT03643510PHASE2COMPLETEDEvaluating Cancer Response to Treatment With Abemaciclib and Fulvestrant in Women With Recurrent Endometrial Cancer
NCT03836157PHASE2WITHDRAWNMirvetuximab Soravtansine (IMGN853) and Bevacizumab in Patients With Endometrial Cancer
NCT05001282PHASE1/PHASE2TERMINATEDA Study to Evaluate ELU001 in Patients With Solid Tumors That Overexpress Folate Receptor Alpha (FRα)

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
CAPIVASERTIB42
IXABEPILONE42
MEGESTROL ACETATE42
TEMSIROLIMUS42
ABEMACICLIB41
BUPIVACAINE41
COPANLISIB41
DURVALUMAB41
FILGRASTIM41
LURBINECTEDIN41
MEDROXYPROGESTERONE ACETATE41
METFORMIN41
MIRVETUXIMAB SORAVTANSINE41
NINTEDANIB41
NIRAPARIB41
PACLITAXEL41
PEGFILGRASTIM41
PEMBROLIZUMAB41
RUXOLITINIB PHOSPHATE41
SELUMETINIB41
SODIUM PERTECHNETATE TC 99M41
SUNITINIB MALATE41
CADONILIMAB32
CEDIRANIB MALEATE32
BRIVANIB ALANINATE31
DALANTERCEPT31
TREBANANIB31
ONAPRISTONE21
UPROSERTIB21
VISTUSERTIB21

Precision-medicine subtype map (CIViC)

Drug × molecular subtype: 2 predictive associations from 2 curated evidence items; also 1 oncogenic.

Molecular subtypeTherapyEffectLevelCIViC
MTOR S2215YSirolimusSensitivity/ResponseCIViC DEID1319
TP53 R175HMDM2 Inhibitor AMGMDS3ResistanceCIViC DEID10076