Prostate adenocarcinoma
diseaseOn this page
Also known as adenocarcinoma of prostateadenocarcinoma of the prostatepradprostate gland adenocarcinoma
Summary
Prostate adenocarcinoma (MONDO:0005082) is a disease with 2 cohort genes and 451 clinical trials. Molecularly, PTEN Mutation confers sensitivity to PI3Kbeta Inhibitor AZD8186 + Enzalutamide + Alpelisib in Prostate Adenocarcinoma (CIViC Level D). Top therapeutic interventions include goserelin, leuprolide, and apalutamide.
At a glance
- Cohort genes: 2
- Clinical trials: 451
- Precision-medicine evidence (CIViC): 1 subtype–drug association
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | prostate adenocarcinoma |
| Mondo ID | MONDO:0005082 |
| EFO | EFO:0000673 |
| DOID | DOID:2526 |
| NCIT | C2919 |
| SNOMED CT | 399490008 |
| UMLS | C0007112 |
| MedGen | 764 |
| Anatomy (UBERON) | UBERON:0002367 |
| Is cancer (heuristic) | no |
Also known as: adenocarcinoma of prostate · adenocarcinoma of the prostate · prad · prostate adenocarcinoma · prostate gland adenocarcinoma
Data availability: 95 intOGen driver records.
Disease family
An umbrella term covering 2 Mondo subtypes.
Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › cancer › carcinoma › adenocarcinoma › prostate adenocarcinoma
Related subtypes (63): epididymal adenocarcinoma, rete testis adenocarcinoma, seminal vesicle adenocarcinoma, ethmoid sinus adenocarcinoma, lacrimal gland adenocarcinoma, papillary adenocarcinoma, fallopian tube adenocarcinoma, bladder adenocarcinoma, ovarian adenocarcinoma, trabecular adenocarcinoma, middle ear adenocarcinoma, bile duct adenocarcinoma, granular cell carcinoma, small intestine adenocarcinoma, urethra adenocarcinoma, villous adenocarcinoma, thymus gland adenocarcinoma, nasal cavity adenocarcinoma, ureter adenocarcinoma, adenocarcinoma in situ, gastroesophageal junction adenocarcinoma, maxillary sinus adenocarcinoma, mucinous adenocarcinoma, acinar cell carcinoma, adenoid cystic carcinoma, breast adenocarcinoma, clear cell adenocarcinoma, colorectal adenocarcinoma, endometrioid adenocarcinoma, esophageal adenocarcinoma, gastric adenocarcinoma, lung adenocarcinoma, renal cell carcinoma, signet ring cell carcinoma, cervical adenocarcinoma, serous adenocarcinoma, endometrium adenocarcinoma, sweat gland carcinoma, cystadenocarcinoma, tubular adenocarcinoma, mesonephric adenocarcinoma, scirrhous adenocarcinoma, pancreatic adenocarcinoma, follicular variant thyroid gland papillary carcinoma, gallbladder adenocarcinoma, hepatoid adenocarcinoma, intestinal type adenocarcinoma, micropapillary serous carcinoma, minor salivary gland adenocarcinoma, poorly differentiated thyroid gland carcinoma, salivary gland basal cell adenocarcinoma, submandibular gland adenocarcinoma, sebaceous adenocarcinoma, hepatocellular carcinoma, parathyroid gland carcinoma, pituitary adenocarcinoma, vaginal adenocarcinoma, Paget disease, diffuse type adenocarcinoma, vulvar adenocarcinoma, thyroid gland adenocarcinoma, gastroesophageal adenocarcinoma, adenoacanthoma
Subtypes (2): prostatic acinar adenocarcinoma, prostate adenoid cystic 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
Mendelian disease overlap and somatic drivers
GenCC: 0 · Orphanet: 17 · OMIM-shared: 0 · Dual-evidence (GWAS+Mendelian): 0
Orphanet rare-disease linkage (cohort genes)
| Gene | Orphanet ID | Rare disease |
|---|---|---|
| MTHFR | Orphanet:395 | Homocystinuria due to methylene tetrahydrofolate reductase deficiency |
| MTHFR | Orphanet:563609 | Isolated anencephaly |
| MTHFR | Orphanet:563612 | Isolated exencephaly |
| PTEN | Orphanet:109 | Bannayan-Riley-Ruvalcaba syndrome |
| PTEN | Orphanet:137608 | Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome |
| PTEN | Orphanet:145 | Hereditary breast and/or ovarian cancer syndrome |
| PTEN | Orphanet:201 | Cowden syndrome |
| PTEN | Orphanet:210548 | Macrocephaly-intellectual disability-autism syndrome |
| PTEN | Orphanet:2969 | Proteus-like syndrome |
| PTEN | Orphanet:494547 | Squamous cell carcinoma of the hypopharynx |
| PTEN | Orphanet:494550 | Squamous cell carcinoma of the larynx |
| PTEN | Orphanet:500464 | Squamous cell carcinoma of the nasal cavity and paranasal sinuses |
| PTEN | Orphanet:500478 | Squamous cell carcinoma of the oropharynx |
| PTEN | Orphanet:502363 | Squamous cell carcinoma of the oral cavity |
| PTEN | Orphanet:502366 | Squamous cell carcinoma of the lip |
| PTEN | Orphanet:65285 | Lhermitte-Duclos disease |
| PTEN | Orphanet:79076 | Juvenile polyposis of infancy |
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 |
|---|---|---|---|---|---|
| MTHFR | HGNC:7436 | ENSG00000177000 | P42898 | Methylenetetrahydrofolate reductase (NADPH) | civic_evidence |
| PTEN | HGNC:9588 | ENSG00000171862 | P60484 | Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN | civic_evidence |
Cohort function summary
Lead sentence per gene, UniProt-curated.
| Symbol | Protein name | Function (lead sentence) |
|---|---|---|
| MTHFR | Methylenetetrahydrofolate reductase (NADPH) | Catalyzes the conversion of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofolate, a cosubstrate for homocysteine remethylation to methionine. |
| PTEN | Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN | Dual-specificity protein phosphatase, dephosphorylating tyrosine-, serine- and threonine-phosphorylated proteins. |
Protein-family classification
Druggable: 2 · Difficult: 0 · Unknown: 0 · Druggable fraction: 1.0
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 |
|---|---|---|---|
| Phosphatase | 1 | 42.0× | 0.047 |
| Enzyme (other) | 1 | 6.0× | 0.160 |
Per-gene assignment
| Symbol | Family | Druggable? | EC | InterPro (top 3) |
|---|---|---|---|---|
| MTHFR | Enzyme (other) | yes | 1.5.1.20 | Mehydrof_redctse-like, Fadh2_euk, FAD-linked_oxidoreductase-like |
| PTEN | Phosphatase | yes | 3.1.3.16 | Tyr_Pase_dom, Tyr_Pase_cat, Tensin_C2-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 |
|---|---|
| apex of heart | 1 |
| corpus epididymis | 1 |
| sural nerve | 1 |
| calcaneal tendon | 1 |
| endothelial cell | 1 |
| sperm | 1 |
Per-gene tissue summary (top 30)
| Symbol | Bgee breadth | FANTOM5 breadth | SCXA | Top tissues |
|---|---|---|---|---|
| MTHFR | 254 | ubiquitous | marker | corpus epididymis, sural nerve, apex of heart |
| PTEN | 256 | ubiquitous | marker | sperm, endothelial cell, calcaneal tendon |
Protein interactions among cohort
Intra-cohort edges: 0.
Hub genes (top 10 by interactor count)
| Symbol | Interactor count |
|---|---|
| PTEN | 11,626 |
| MTHFR | 3,492 |
Structural data
PDB: 2 · AlphaFold-only: 0 · No structure: 0
Cohort genes with PDB structures (top 30)
| Symbol | UniProt | PDB entries |
|---|---|---|
| PTEN | P60484 | 12 |
| MTHFR | P42898 | 4 |
Function
Pathway analysis
Distinct Reactome pathways touched by cohort: 17. 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 |
|---|---|---|---|---|
| PTEN Loss of Function in Cancer | 1 | 2855.0× | 0.006 | PTEN |
| Regulation of PTEN mRNA translation | 1 | 571.0× | 0.011 | PTEN |
| Regulation of PTEN localization | 1 | 519.1× | 0.011 | PTEN |
| Metabolism of folate and pterines | 1 | 317.2× | 0.013 | MTHFR |
| Synthesis of IP3 and IP4 in the cytosol | 1 | 211.5× | 0.015 | PTEN |
| Transcriptional Regulation by MECP2 | 1 | 158.6× | 0.015 | PTEN |
| Negative regulation of the PI3K/AKT network | 1 | 139.3× | 0.015 | PTEN |
| Ovarian tumor domain proteases | 1 | 139.3× | 0.015 | PTEN |
| Synthesis of PIPs at the plasma membrane | 1 | 105.7× | 0.016 | PTEN |
| Regulation of PTEN stability and activity | 1 | 92.1× | 0.016 | PTEN |
| Metabolism of water-soluble vitamins and cofactors | 1 | 90.6× | 0.016 | MTHFR |
| Regulation of PTEN gene transcription | 1 | 89.2× | 0.016 | PTEN |
| TP53 Regulates Metabolic Genes | 1 | 64.9× | 0.019 | PTEN |
| Downstream TCR signaling | 1 | 64.2× | 0.019 | PTEN |
| Metabolism of vitamins and cofactors | 1 | 58.3× | 0.019 | MTHFR |
| Ub-specific processing proteases | 1 | 26.6× | 0.040 | PTEN |
| Metabolism | 1 | 5.8× | 0.165 | MTHFR |
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 |
|---|---|---|---|---|
| response to vitamin B2 | 1 | 4213.0× | 0.004 | MTHFR |
| negative regulation of synaptic vesicle clustering | 1 | 4213.0× | 0.004 | PTEN |
| S-adenosylmethionine metabolic process | 1 | 2808.7× | 0.004 | MTHFR |
| negative regulation of keratinocyte migration | 1 | 2808.7× | 0.004 | PTEN |
| rhythmic synaptic transmission | 1 | 2106.5× | 0.004 | PTEN |
| obsolete methionine biosynthetic process | 1 | 1685.2× | 0.004 | MTHFR |
| L-methionine metabolic process | 1 | 1404.3× | 0.004 | MTHFR |
| central nervous system myelin maintenance | 1 | 1404.3× | 0.004 | PTEN |
| response to folic acid | 1 | 1203.7× | 0.004 | MTHFR |
| negative regulation of cell cycle G1/S phase transition | 1 | 1203.7× | 0.004 | PTEN |
| negative regulation of wound healing, spreading of epidermal cells | 1 | 1203.7× | 0.004 | PTEN |
| spindle assembly involved in female meiosis | 1 | 936.2× | 0.004 | PTEN |
| central nervous system neuron axonogenesis | 1 | 936.2× | 0.004 | PTEN |
| homocysteine metabolic process | 1 | 936.2× | 0.004 | MTHFR |
| postsynaptic density assembly | 1 | 936.2× | 0.004 | PTEN |
| neuron-neuron synaptic transmission | 1 | 842.6× | 0.004 | PTEN |
| negative regulation of peptidyl-serine phosphorylation | 1 | 842.6× | 0.004 | PTEN |
| tetrahydrofolate interconversion | 1 | 842.6× | 0.004 | MTHFR |
| negative regulation of cell size | 1 | 842.6× | 0.004 | PTEN |
| presynaptic membrane assembly | 1 | 842.6× | 0.004 | PTEN |
| negative regulation of organ growth | 1 | 702.2× | 0.004 | PTEN |
| forebrain morphogenesis | 1 | 702.2× | 0.004 | PTEN |
| multicellular organismal response to stress | 1 | 648.1× | 0.004 | PTEN |
| negative regulation of axonogenesis | 1 | 648.1× | 0.004 | PTEN |
| heterochromatin organization | 1 | 648.1× | 0.004 | MTHFR |
| cellular response to electrical stimulus | 1 | 648.1× | 0.004 | PTEN |
| negative regulation of excitatory postsynaptic potential | 1 | 648.1× | 0.004 | PTEN |
| maternal behavior | 1 | 561.7× | 0.004 | PTEN |
| prepulse inhibition | 1 | 561.7× | 0.004 | PTEN |
| locomotor rhythm | 1 | 526.6× | 0.004 | PTEN |
Therapeutics
Drugs indicated for this disease
10 approved, 34 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.
| Drug | Development status |
|---|---|
| Abiraterone Acetate | Approved (phase 4) |
| Apalutamide | Approved (phase 4) |
| Cabazitaxel | Approved (phase 4) |
| Darolutamide | Approved (phase 4) |
| Dutasteride | Approved (phase 4) |
| Enzalutamide | Approved (phase 4) |
| Finasteride | Approved (phase 4) |
| Flutamide | Approved (phase 4) |
| Nilutamide | Approved (phase 4) |
| Relugolix | Approved (phase 4) |
| Abiraterone | Phase 3 (in late-stage trials) |
| Alendronic Acid | Phase 3 (in late-stage trials) |
| Atezolizumab | Phase 3 (in late-stage trials) |
| Atorvastatin | Phase 3 (in late-stage trials) |
| Atrasentan | Phase 3 (in late-stage trials) |
| Bevacizumab | Phase 3 (in late-stage trials) |
| Bicalutamide | Phase 3 (in late-stage trials) |
| Buserelin | Phase 3 (in late-stage trials) |
| CTT-1057 | Phase 3 (in late-stage trials) |
| Cholecalciferol | Phase 3 (in late-stage trials) |
| Cyproterone Acetate | Phase 3 (in late-stage trials) |
| Dasatinib Anhydrous | Phase 3 (in late-stage trials) |
| Degarelix | Phase 3 (in late-stage trials) |
| Dexamethasone | Phase 3 (in late-stage trials) |
| Estramustine | Phase 3 (in late-stage trials) |
| Fludrocortisone Acetate | Phase 3 (in late-stage trials) |
| Goserelin | Phase 3 (in late-stage trials) |
| Histrelin | Phase 3 (in late-stage trials) |
| Hydrocortisone | Phase 3 (in late-stage trials) |
| Leuprolide | Phase 3 (in late-stage trials) |
| Medroxyprogesterone Acetate | Phase 3 (in late-stage trials) |
| Meloxicam | Phase 3 (in late-stage trials) |
| Mitoxantrone | Phase 3 (in late-stage trials) |
| Olaparib | Phase 3 (in late-stage trials) |
| Opevesostat | Phase 3 (in late-stage trials) |
| Pembrolizumab | Phase 3 (in late-stage trials) |
| Perflutren | Phase 3 (in late-stage trials) |
| Prednisolone | Phase 3 (in late-stage trials) |
| Prednisone | Phase 3 (in late-stage trials) |
| Rosiglitazone | Phase 3 (in late-stage trials) |
| Sipuleucel-T | Phase 3 (in late-stage trials) |
| Sunitinib | Phase 3 (in late-stage trials) |
| Tasquinimod | Phase 3 (in late-stage trials) |
| Triptorelin | Phase 3 (in late-stage trials) |
Earlier-phase candidates (phase 2, investigational — efficacy not yet established): ANTINEOPLASTON A10, Afatinib, Alisertib, Amifostine, Ascorbic Acid, Aspirin, Axitinib, Azacitidine, Cabozantinib, Calcitriol, Capivasertib, Carboplatin, Cediranib, Celecoxib, Cetuximab, Doconexent, Doxorubicin, Durvalumab, Erdafitinib, Ergocalciferol, Etoposide, Exisulind, Fenretinide, Figitumumab, Flibanserin, Fulvestrant, Furosemide, Ganetespib, Golimumab, INTERFERON ALFA-2B, Icosapent, Incomplete Freund’S Adjuvant, Indomethacin, Ipilimumab, Isosorbide, Itraconazole, Ixabepilone, Ketoconazole, Lenalidomide, Linsitinib, Lycopene, Metformin, Mifepristone, Naproxen, Neratinib, Nintedanib, Niraparib, Nivolumab, Orteronel, Paclitaxel, Paclitaxel Poliglumex, Patupilone, Pazopanib, Perifosine, Piflufolastat, Relacorilant, Rilimogene Galvacirepvec, Rintatolimod, Sargramostim, Selegiline, Siltuximab, Sodium Fluoride, Sorafenib, Sulforaphane, Talazoparib, Tanespimycin, Testosterone Cypionate, Testosterone Enanthate, Thalidomide, Tivantinib, Tocilizumab, Trebananib, Tremelimumab, Tretinoin, Trilostane, Vorinostat, Zibotentan, Zimberelimab.
Drug target analysis
Approved (phase 4): 0 · Phase ≥3: 0 · Phased (≥1): 0 · Undrugged: 2
Druggability breadth: 1 of 2 evidence-associated genes (50%) have a ChEMBL target (buckets above are over the deeply-mined display cohort).
Top cohort targets by molecule count
| Symbol | Molecules | Max phase |
|---|---|---|
| MTHFR | 0 | 0 |
| PTEN | 0 | 0 |
Bioactivity and enzyme data
Enzyme cohort genes (≥1 EC): 2.
Cohort genes with ChEMBL bioactivity (full, sorted by assay count)
| Symbol | Assays | Type breakdown |
|---|---|---|
| PTEN | 8 | Binding:8 |
Cohort enzymes (BRENDA EC)
| Symbol | EC numbers | Names |
|---|---|---|
| MTHFR | 1.5.1.20, 1.5.1.53 | methylenetetrahydrofolate reductase [NAD(P)H], methylenetetrahydrofolate reductase (NADPH) |
| PTEN | 3.1.3.16, 3.1.3.67 | protein-serine/threonine phosphatase, phosphatidylinositol-3,4,5-trisphosphate 3-phosphatase |
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
0 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.
Druggability pyramid
Cohort genes binned by druggability tier (high → low):
| Tier | Definition | Genes | Symbols |
|---|---|---|---|
| A | Approved (phase 4 drug) | 0 | |
| B | Phased (≥1) drug, not yet approved | 0 | |
| C | Druggable family + PDB, no drug | 2 | MTHFR, PTEN |
| D | Druggable family + AlphaFold only, no drug | 0 | |
| E | Difficult family or no structure, no drug | 0 |
Undrugged target profiles
2 cohort genes are undrugged. Ranked by ‘starting-point quality’ (assay depth + drugged-partner adjacency).
| Symbol | ChEMBL assays | Drugged partners (top 3) |
|---|---|---|
| MTHFR | 0 | — |
| PTEN | 8 | — |
Clinical trials & evidence
Clinical trials
Clinical trials: 451.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| PHASE2 | 192 |
| Not specified | 135 |
| PHASE1 | 48 |
| PHASE3 | 32 |
| PHASE1/PHASE2 | 25 |
| EARLY_PHASE1 | 9 |
| PHASE2/PHASE3 | 6 |
| PHASE4 | 4 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT05919329 | PHASE4 | RECRUITING | Evaluation of the Change in PSMA Expression in Prostate Cancer in Response to Hormonal Therapy |
| NCT01661166 | PHASE4 | COMPLETED | A Study of Effects of Fesoterodine in Men at High Risk for Overactive Bladder/Detrusor Overactivity Post Robotic-Assisted Lap. Prostatectomy |
| NCT02025361 | PHASE4 | COMPLETED | Impact of Local Anesthesia Type on Cancer Detection Rate in Transrectal Ultrasound Guided Prostate Biopsy |
| NCT05803096 | PHASE4 | COMPLETED | Self-Administered Nitrous Oxide (SANO) During Transrectal Prostate Biopsy to Reduce Patient Anxiety and Pain |
| NCT01952223 | PHASE3 | ACTIVE_NOT_RECRUITING | A Phase III of Cabazitaxel and Pelvic Radiotherapy in Localized Prostate Cancer and High-risk Features of Relapse |
| NCT03367702 | PHASE3 | ACTIVE_NOT_RECRUITING | Stereotactic Body Radiation Therapy or Intensity-Modulated Radiation Therapy in Treating Patients With Stage IIA-B Prostate Cancer |
| NCT04134260 | PHASE3 | RECRUITING | Testing the Addition of the Drug Apalutamide to the Usual Hormone Therapy and Radiation Therapy After Surgery for Prostate Cancer, INNOVATE Trial |
| NCT04423211 | PHASE3 | RECRUITING | Treating Prostate Cancer That Has Come Back After Surgery With Apalutamide and Targeted Radiation Based on PET Imaging |
| NCT04446117 | PHASE3 | ACTIVE_NOT_RECRUITING | Study of Cabozantinib in Combination With Atezolizumab Versus Second NHT in Subjects With mCRPC |
| NCT04455750 | PHASE3 | ACTIVE_NOT_RECRUITING | A Clinical Study Evaluating The Benefit of Adding Rucaparib to Enzalutamide for Men With Metastatic Prostate Cancer That Has Become Resistant To Testosterone-Deprivation Therapy |
| NCT04513717 | PHASE3 | ACTIVE_NOT_RECRUITING | Two Studies for Patients With High Risk Prostate Cancer Testing Less Intense Treatment for Patients With a Low Gene Risk Score and Testing a More Intense Treatment for Patients With a High Gene Risk Score, The PREDICT-RT Trial |
| NCT05050084 | PHASE3 | ACTIVE_NOT_RECRUITING | Two Studies for Patients With Unfavorable Intermediate Risk Prostate Cancer Testing Less Intense Treatment for Patients With a Low Gene Risk Score and Testing a More Intense Treatment for Patients With a Higher Gene Risk Score, The Guidance Trial |
| NCT05796973 | PHASE3 | RECRUITING | Measuring Oncological Value of Exercise and Statin |
| NCT05946213 | PHASE3 | RECRUITING | Testing Shorter Duration Radiation Therapy Versus the Usual Radiation Therapy in Patients With High Risk Prostate Cancer |
| NCT06205316 | PHASE3 | RECRUITING | SBRT Versus Hypofractionated Radiotherapy for Biochemically Recurrent or Oligometastatic Prostate Adenocarcinoma |
| NCT06235151 | PHASE3 | RECRUITING | Copper Cu 64 PSMA I&T PET Imaging in Men With Newly Diagnosed Prostate Cancer |
| NCT06931340 | PHASE3 | RECRUITING | Testing the Addition of Docetaxel (Chemotherapy) to the Usual Treatment (Hormonal Therapy and Apalutamide) for Metastatic Prostate Cancer, ASPIRE Trial |
| NCT07200830 | PHASE3 | NOT_YET_RECRUITING | Testing Different Dosing Schedules of the Anti-cancer Drug, Lutetium 177Lu PSMA RLT and Its Effect on Patients With Advanced Prostate Cancer, RECIPROCAL Trial |
| NCT07574489 | PHASE2/PHASE3 | NOT_YET_RECRUITING | Whole Versus Partial Gland Boost During Prostate SBRT |
| NCT00110214 | PHASE3 | COMPLETED | Docetaxel and Prednisone With or Without Bevacizumab in Treating Patients With Prostate Cancer That Did Not Respond to Hormone Therapy |
| NCT00182052 | PHASE3 | COMPLETED | Rosiglitazone (Avandia) vs. Placebo for Androgen Dependent Prostate Cancer |
| NCT00764166 | PHASE3 | UNKNOWN | A Prospective Randomized Phase III Study Comparing Hormonal Therapy +/-Docetaxel |
| NCT01394263 | PHASE3 | COMPLETED | Study of Histrelin Subdermal Implant in Patients With Prostate Cancer |
| NCT01697384 | PHASE3 | COMPLETED | Study to Evaluate Efficacy and Safety of Histrelin Subdermal Implant in Men With Advanced Prostate Cancer |
| NCT01949337 | PHASE3 | UNKNOWN | Enzalutamide With or Without Abiraterone and Prednisone in Treating Patients With Castration-Resistant Metastatic Prostate Cancer |
| NCT02175212 | PHASE3 | COMPLETED | Clinical Trials of Adjuvant Androgen Deprivation in Localized Prostate Cancer |
| NCT02258087 | PHASE2/PHASE3 | UNKNOWN | HDR vs LDR Brachytherapy as Monotherapy in the Treatment of Localized Prostate Cancer. |
| NCT02624518 | PHASE2/PHASE3 | COMPLETED | 68Ga-RM2 PET/MRI in Biochemically Recurrent Prostate Cancer |
| NCT02673151 | PHASE2/PHASE3 | COMPLETED | 68Ga-PSMA PET/CT in Detecting Prostate Cancer Recurrence in Patients With Elevated PSA After Initial Treatment |
| NCT02678351 | PHASE2/PHASE3 | COMPLETED | 68Ga-PSMA-11 PET/MRI in Finding Tumors in Patients With Intermediate or High-Risk Prostate Cancer Undergoing Surgery |
| NCT02940262 | PHASE3 | COMPLETED | Gallium Ga 68-labeled PSMA-11 PET/CT in Detecting Recurrent Prostate Cancer in Patients After Initial Therapy |
| NCT03070886 | PHASE2/PHASE3 | COMPLETED | Antiandrogen Therapy and Radiation Therapy With or Without Docetaxel in Treating Patients With Prostate Cancer That Has Been Removed by Surgery |
| NCT03274687 | PHASE3 | COMPLETED | Hypofractionated Radiation Therapy or Conventional Radiation Therapy After Surgery in Treating Patients With Prostate Cancer |
| NCT03327662 | PHASE3 | TERMINATED | Utilising CTC Counts to Optimize Systemic Therapy of Metastatic Prostate Cancer |
| NCT03404648 | PHASE3 | COMPLETED | Staging Prostate Cancer With Hybrid C11-Choline PET/MR and mpMRI |
| NCT03535675 | PHASE3 | TERMINATED | Muscadine Plus (MPX) In Men With Prostate Cancer |
| NCT03686683 | PHASE3 | COMPLETED | Open- Label Trial of Sipuleucel-T Administered to Active Surveillance Patients for Newly Diagnosed Prostate Cancer |
| NCT03739684 | PHASE3 | COMPLETED | Study of 18F-DCFPyL PET/CT Imaging in Patients With Suspected Recurrence of Prostate Cancer |
| NCT04914195 | PHASE3 | COMPLETED | Leuprolide Acetate 3.75 mg Depot Injection for Patients With Advanced Prostate Cancer |
| NCT05197257 | PHASE3 | COMPLETED | 68Ga-PSMA-11 PET in Patients With Prostate Cancer |
Drugs tested across these trials (top 30)
Precision-medicine subtype map (CIViC)
Drug × molecular subtype: 1 predictive associations from 1 curated evidence items; also 1 predisposing, 1 prognostic.
| Molecular subtype | Therapy | Effect | Level | CIViC |
|---|---|---|---|---|
| PTEN Mutation | PI3Kbeta Inhibitor AZD8186 + Enzalutamide + Alpelisib | Sensitivity/Response | CIViC D | EID1522 |
Related Atlas pages
- Cohort genes: MTHFR, PTEN
- Drugs: Goserelin, Leuprolide, Apalutamide, Degarelix, Bicalutamide, Talazoparib, Enzalutamide, GALLIUM GA 68 GOZETOTIDE, Relugolix, Flutamide, Abiraterone Acetate, Histrelin, Triptorelin, Cabazitaxel, FLOTUFOLASTAT F-18 GALLIUM, FLUCICLOVINE F18, LUTETIUM LU-177 VIPIVOTIDE TETRAXETAN, Phenelzine, Sipuleucel-T, Abiraterone, Cabozantinib, Ixabepilone, Nilutamide, PIFLUFOLASTAT F18, RADIUM RA 223 DICHLORIDE, Atorvastatin, Buserelin, Darolutamide, Erdafitinib, Gonadorelin