Carcinoma
diseaseOn this page
Also known as carcinoma, malignantepithelial carcinomaepitheliomaepithelioma malignantmalignant epithelial neoplasmmalignant epithelial tumormalignant epithelial tumourmalignant epitheliomaOther carcinoma
Summary
Carcinoma (MONDO:0004993) is a cancer (an umbrella term covering 49 Mondo subtypes) with 1 cohort gene (1 CIViC-evidence somatic driver) and 252 clinical trials. Molecularly, BAG4::FGFR1 Fusion confers sensitivity to Fexagratinib in Carcinoma (CIViC Level C). Top therapeutic interventions include fluorouracil, sorafenib, and irinotecan.
At a glance
- Classification: Cancer
- Umbrella term: 49 Mondo subtypes
- Cohort genes: 1
- Clinical trials: 252
- 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 | carcinoma |
| Mondo ID | MONDO:0004993 |
| EFO | EFO:0000313 |
| MeSH | D002277 |
| DOID | DOID:305 |
| NCIT | C2916 |
| SNOMED CT | 722688002 |
| UMLS | C0007097 |
| MedGen | 2867 |
| Is cancer (heuristic) | yes |
Also known as: carcinoma · carcinoma, malignant · epithelial carcinoma · epithelioma · epithelioma malignant · malignant epithelial neoplasm · malignant epithelial tumor · malignant epithelial tumour · malignant epithelioma · Other carcinoma
Disease family
An umbrella term covering 49 Mondo subtypes.
Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › cancer › carcinoma
Related subtypes (32): respiratory system cancer, immune system cancer, musculoskeletal system cancer, integumentary system cancer, peritoneum cancer, cardiovascular cancer, reproductive system cancer, malignant giant cell tumor, digestive system cancer, lipomatous cancer, thoracic cancer, malignant glomus tumor, malignant mesenchymoma, sarcoma, blastoma, head and neck cancer, malignant mixed neoplasm, nervous system cancer, retroperitoneal cancer, malignant germ cell tumor, malignant mesothelioma, malignant urinary system neoplasm, childhood malignant neoplasm, anaplastic cancer, malignant spindle cell neoplasm, high grade malignant neoplasm, malignant endocrine neoplasm, malignant soft tissue neoplasm, secondary malignant neoplasm, refractory malignant neoplasm, malignant adenoma, cancer of unknown primary site
Subtypes (49): retroperitoneum carcinoma, head and neck carcinoma, peritoneal carcinoma, neuroendocrine carcinoma, laryngeal carcinoma, bone carcinoma, carcinoma ex pleomorphic adenoma, scrotal carcinoma, skin carcinoma, malignant myoepithelioma, trachea carcinoma, epithelial-myoepithelial carcinoma, lipid-rich carcinoma, comedocarcinoma, in situ carcinoma, adenocarcinoma, urinary bladder carcinoma, breast carcinoma, squamous cell carcinoma, lung carcinoma, prostate carcinoma, renal carcinoma, uterine carcinoma, vulvar carcinoma, large cell carcinoma, undifferentiated carcinoma, basaloid carcinoma, cribriform carcinoma, digestive system carcinoma, fallopian tube carcinoma, penile carcinoma, sarcomatoid carcinoma, thymic carcinoma, transitional cell carcinoma, ureter carcinoma, papillary carcinoma, Krebs 2 carcinoma, thyroid gland carcinoma, vaginal carcinoma, choroid plexus carcinoma, malignant epithelial tumor of ovary, mucin-producing carcinoma, basal cell carcinoma, carcinoma of urethra, combined carcinoid and adenocarcinoma, secondary carcinoma, invasive carcinoma, glycogen-rich carcinoma, lymph node 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: 4 · OMIM-shared: 0 · Dual-evidence (GWAS+Mendelian): 0
Somatic driver evidence (intOGen + CIViC, cohort fanout)
| Gene | intOGen role | Cancer types | CIViC |
|---|---|---|---|
| ERBB2 | Act | BLCA,BRCA,CESC,CHOL,COADREAD,EGC,ESCA,ESCC,LMS,LUAD,NSCLC,OVT,PRCC,READ,STAD,UCEC | CIViC #20 |
Orphanet rare-disease linkage (cohort genes)
| Gene | Orphanet ID | Rare disease |
|---|---|---|
| ERBB2 | Orphanet:213726 | Serous carcinoma of the corpus uteri |
| ERBB2 | Orphanet:2800 | Extramammary Paget disease |
| ERBB2 | Orphanet:388 | Hirschsprung disease |
| ERBB2 | Orphanet:99976 | Adenocarcinoma of the oesophagus and oesophagogastric junction |
Cohort genes → proteins
1 cohort genes, 1 distinct canonical proteins.
Evidence partition
| Subset | Genes |
|---|---|
| civic_only | 1 |
Cohort genes (full)
| Symbol | HGNC | Ensembl | UniProt | Name | Evidence |
|---|---|---|---|---|---|
| ERBB2 | HGNC:3430 | ENSG00000141736 | P04626 | Receptor tyrosine-protein kinase erbB-2 | civic_evidence |
Cohort function summary
Lead sentence per gene, UniProt-curated.
| Symbol | Protein name | Function (lead sentence) |
|---|---|---|
| ERBB2 | Receptor tyrosine-protein kinase erbB-2 | Protein tyrosine kinase that is part of several cell surface receptor complexes, but that apparently needs a coreceptor for ligand binding. |
Protein-family classification
Druggable: 1 · 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 |
|---|---|---|---|
| Kinase | 1 | 27.7× | 0.036 |
Per-gene assignment
| Symbol | Family | Druggable? | EC | InterPro (top 3) |
|---|---|---|---|---|
| ERBB2 | Kinase | yes | 2.7.10.1 | Rcpt_L-dom, Prot_kinase_dom, Ser-Thr/Tyr_kinase_cat_dom |
Expression context
Cohort genes with no expression data: 0.
1 cohort gene 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) | 1 |
| unknown | 0 |
Top tissues across cohort
| Tissue | Cohort genes |
|---|---|
| lower esophagus mucosa | 1 |
| right uterine tube | 1 |
| sural nerve | 1 |
Per-gene tissue summary (top 30)
| Symbol | Bgee breadth | FANTOM5 breadth | SCXA | Top tissues |
|---|---|---|---|---|
| ERBB2 | 276 | ubiquitous | marker | lower esophagus mucosa, right uterine tube, sural nerve |
Protein interactions among cohort
Intra-cohort edges: 0.
Hub genes (top 10 by interactor count)
| Symbol | Interactor count |
|---|---|
| ERBB2 | 9,659 |
Structural data
PDB: 1 · AlphaFold-only: 0 · No structure: 0
Cohort genes with PDB structures (top 30)
| Symbol | UniProt | PDB entries |
|---|---|---|
| ERBB2 | P04626 | 63 |
Function
Pathway analysis
Distinct Reactome pathways touched by cohort: 33. Enrichment computed across 1 evidence-associated genes (1 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 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.
| Pathway | Cohort genes | Fold | FDR | Sample cohort genes |
|---|---|---|---|---|
| PLCG1 events in ERBB2 signaling | 1 | 2855.0× | 0.001 | ERBB2 |
| Drug-mediated inhibition of ERBB2 signaling | 1 | 2855.0× | 0.001 | ERBB2 |
| Resistance of ERBB2 KD mutants to trastuzumab | 1 | 2855.0× | 0.001 | ERBB2 |
| Resistance of ERBB2 KD mutants to sapitinib | 1 | 2855.0× | 0.001 | ERBB2 |
| Resistance of ERBB2 KD mutants to tesevatinib | 1 | 2855.0× | 0.001 | ERBB2 |
| Resistance of ERBB2 KD mutants to neratinib | 1 | 2855.0× | 0.001 | ERBB2 |
| Resistance of ERBB2 KD mutants to osimertinib | 1 | 2855.0× | 0.001 | ERBB2 |
| Resistance of ERBB2 KD mutants to afatinib | 1 | 2855.0× | 0.001 | ERBB2 |
| Resistance of ERBB2 KD mutants to AEE788 | 1 | 2855.0× | 0.001 | ERBB2 |
| Resistance of ERBB2 KD mutants to lapatinib | 1 | 2855.0× | 0.001 | ERBB2 |
| Drug resistance in ERBB2 TMD/JMD mutants | 1 | 2855.0× | 0.001 | ERBB2 |
| GRB7 events in ERBB2 signaling | 1 | 1903.3× | 0.001 | ERBB2 |
| Constitutive Signaling by Overexpressed ERBB2 | 1 | 951.7× | 0.002 | ERBB2 |
| Downregulation of ERBB2:ERBB3 signaling | 1 | 815.7× | 0.002 | ERBB2 |
| ERBB2 Activates PTK6 Signaling | 1 | 815.7× | 0.002 | ERBB2 |
| TFAP2 (AP-2) family regulates transcription of growth factors and their receptors | 1 | 761.3× | 0.002 | ERBB2 |
| Developmental Lineage of Mammary Stem Cells | 1 | 761.3× | 0.002 | ERBB2 |
| ERBB2 Regulates Cell Motility | 1 | 713.8× | 0.002 | ERBB2 |
| PI3K events in ERBB2 signaling | 1 | 671.8× | 0.002 | ERBB2 |
| Signaling by ERBB2 ECD mutants | 1 | 671.8× | 0.002 | ERBB2 |
| GRB2 events in ERBB2 signaling | 1 | 634.4× | 0.002 | ERBB2 |
| Sema4D induced cell migration and growth-cone collapse | 1 | 571.0× | 0.003 | ERBB2 |
| Developmental Lineage of Mammary Gland Myoepithelial Cells | 1 | 543.8× | 0.003 | ERBB2 |
| SHC1 events in ERBB2 signaling | 1 | 475.8× | 0.003 | ERBB2 |
| Signaling by ERBB2 TMD/JMD mutants | 1 | 475.8× | 0.003 | ERBB2 |
| Developmental Lineage of Mammary Gland Luminal Epithelial Cells | 1 | 456.8× | 0.003 | ERBB2 |
| Signaling by ERBB2 KD Mutants | 1 | 423.0× | 0.003 | ERBB2 |
| Downregulation of ERBB2 signaling | 1 | 380.7× | 0.003 | ERBB2 |
| Signaling by ERBB2 | 1 | 346.1× | 0.003 | ERBB2 |
| Constitutive Signaling by Aberrant PI3K in Cancer | 1 | 126.9× | 0.009 | ERBB2 |
GO biological processes by enrichment
Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.
| GO term | Cohort genes | Fold | FDR | Sample cohort genes |
|---|---|---|---|---|
| immature T cell proliferation in thymus | 1 | 3370.4× | 0.004 | ERBB2 |
| negative regulation of immature T cell proliferation in thymus | 1 | 2808.7× | 0.004 | ERBB2 |
| ERBB2-ERBB4 signaling pathway | 1 | 2808.7× | 0.004 | ERBB2 |
| regulation of microtubule-based process | 1 | 1872.4× | 0.004 | ERBB2 |
| ERBB2-ERBB3 signaling pathway | 1 | 1685.2× | 0.004 | ERBB2 |
| ERBB2-EGFR signaling pathway | 1 | 1685.2× | 0.004 | ERBB2 |
| enzyme-linked receptor protein signaling pathway | 1 | 1296.3× | 0.004 | ERBB2 |
| Schwann cell development | 1 | 1053.2× | 0.005 | ERBB2 |
| neurotransmitter receptor localization to postsynaptic specialization membrane | 1 | 802.5× | 0.005 | ERBB2 |
| motor neuron axon guidance | 1 | 702.2× | 0.005 | ERBB2 |
| positive regulation of MAP kinase activity | 1 | 648.1× | 0.005 | ERBB2 |
| positive regulation of transcription by RNA polymerase I | 1 | 648.1× | 0.005 | ERBB2 |
| positive regulation of Rho protein signal transduction | 1 | 581.1× | 0.005 | ERBB2 |
| regulation of ERK1 and ERK2 cascade | 1 | 581.1× | 0.005 | ERBB2 |
| positive regulation of protein targeting to membrane | 1 | 561.7× | 0.005 | ERBB2 |
| neuromuscular junction development | 1 | 526.6× | 0.005 | ERBB2 |
| peptidyl-tyrosine phosphorylation | 1 | 421.3× | 0.005 | ERBB2 |
| regulation of angiogenesis | 1 | 421.3× | 0.005 | ERBB2 |
| oligodendrocyte differentiation | 1 | 421.3× | 0.005 | ERBB2 |
| semaphorin-plexin signaling pathway | 1 | 401.2× | 0.005 | ERBB2 |
| cellular response to growth factor stimulus | 1 | 318.0× | 0.006 | ERBB2 |
| cellular response to epidermal growth factor stimulus | 1 | 318.0× | 0.006 | ERBB2 |
| positive regulation of cell adhesion | 1 | 271.8× | 0.006 | ERBB2 |
| myelination | 1 | 251.5× | 0.006 | ERBB2 |
| epidermal growth factor receptor signaling pathway | 1 | 247.8× | 0.006 | ERBB2 |
| positive regulation of epithelial cell proliferation | 1 | 244.2× | 0.006 | ERBB2 |
| wound healing | 1 | 227.7× | 0.006 | ERBB2 |
| positive regulation of translation | 1 | 227.7× | 0.006 | ERBB2 |
| phosphatidylinositol 3-kinase/protein kinase B signal transduction | 1 | 210.7× | 0.007 | ERBB2 |
| positive regulation of cell growth | 1 | 183.2× | 0.007 | ERBB2 |
Therapeutics
Drugs indicated for this disease
6 approved, 30 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.
| Drug | Development status |
|---|---|
| Bicalutamide | Approved (phase 4) |
| Flutamide | Approved (phase 4) |
| Melphalan | Approved (phase 4) |
| Paclitaxel | Approved (phase 4) |
| Thiotepa | Approved (phase 4) |
| Valrubicin | Approved (phase 4) |
| Brigatinib | Phase 3 (in late-stage trials) |
| Brivanib | Phase 3 (in late-stage trials) |
| Capecitabine | Phase 3 (in late-stage trials) |
| Carboplatin | Phase 3 (in late-stage trials) |
| Cisplatin | Phase 3 (in late-stage trials) |
| Crizotinib | Phase 3 (in late-stage trials) |
| Denosumab | Phase 3 (in late-stage trials) |
| Doxorubicin | Phase 3 (in late-stage trials) |
| Escitalopram | Phase 3 (in late-stage trials) |
| Etoposide | Phase 3 (in late-stage trials) |
| Etoposide Phosphate | Phase 3 (in late-stage trials) |
| Everolimus | Phase 3 (in late-stage trials) |
| Fish Oil Triglycerides | Phase 3 (in late-stage trials) |
| Fluorouracil | Phase 3 (in late-stage trials) |
| Gemcitabine | Phase 3 (in late-stage trials) |
| Hydroxyurea | Phase 3 (in late-stage trials) |
| Ifosfamide | Phase 3 (in late-stage trials) |
| Mitomycin | Phase 3 (in late-stage trials) |
| Mitotane | Phase 3 (in late-stage trials) |
| Nelfinavir | Phase 3 (in late-stage trials) |
| Nimotuzumab | Phase 3 (in late-stage trials) |
| Olaparib | Phase 3 (in late-stage trials) |
| Oxaliplatin | Phase 3 (in late-stage trials) |
| Pembrolizumab | Phase 3 (in late-stage trials) |
| Pemetrexed | Phase 3 (in late-stage trials) |
| Porfiromycin | Phase 3 (in late-stage trials) |
| Sorafenib | Phase 3 (in late-stage trials) |
| Soybean Oil | Phase 3 (in late-stage trials) |
| Streptozocin | Phase 3 (in late-stage trials) |
| Vinorelbine | Phase 3 (in late-stage trials) |
Earlier-phase candidates (phase 2, investigational — efficacy not yet established): ANTINEOPLASTON A10, Aldesleukin, Anastrozole, Atezolizumab, Bavituximab, Belagenpumatucel-L, Belinostat, Bevacizumab, Cabozantinib, Catequentinib, Ceralasertib, Cetuximab, Dacomitinib Anhydrous, Diclofenac, Dostarlimab, Enzalutamide, Erlotinib, Filgrastim, Fulvestrant, Icotinib, Ingenol Mebutate, Ipilimumab, Irinotecan, Letrozole, Lidocaine, Metformin, Nicotine, Nivolumab, Osimertinib, Panitumumab, Pravastatin, Ribociclib, Rivoceranib, Romiplostim, Savolitinib, Sunitinib, Surufatinib, Tislelizumab, Tolvaptan, Toripalimab, Trastuzumab.
Drug target analysis
Approved (phase 4): 1 · Phase ≥3: 1 · Phased (≥1): 1 · Undrugged: 0
Druggability breadth: 1 of 1 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 |
|---|---|
| ERBB2 | CLOTRIMAZOLE |
Top cohort targets by molecule count
| Symbol | Molecules | Max phase |
|---|---|---|
| ERBB2 | 83 | 4 |
Drugs targeting cohort genes (top 30)
| Molecule | Max phase | Targets in cohort |
|---|---|---|
| CLOTRIMAZOLE | 4 | ERBB2 |
| ERLOTINIB HYDROCHLORIDE | 4 | ERBB2 |
| PONATINIB | 4 | ERBB2 |
| AFATINIB | 4 | ERBB2 |
| LAPATINIB DITOSYLATE | 4 | ERBB2 |
| SORAFENIB | 4 | ERBB2 |
| NERATINIB | 4 | ERBB2 |
| IBRUTINIB | 4 | ERBB2 |
| AFATINIB DIMALEATE | 4 | ERBB2 |
| CABOZANTINIB | 4 | ERBB2 |
| DACOMITINIB | 4 | ERBB2 |
| DACOMITINIB ANHYDROUS | 4 | ERBB2 |
| VANDETANIB | 4 | ERBB2 |
| TRIBROMSALAN | 4 | ERBB2 |
| BOSUTINIB | 4 | ERBB2 |
| BITHIONOL | 4 | ERBB2 |
| ASTEMIZOLE | 4 | ERBB2 |
| EBASTINE | 4 | ERBB2 |
| OSIMERTINIB | 4 | ERBB2 |
| BRIGATINIB | 4 | ERBB2 |
| ACALABRUTINIB | 4 | ERBB2 |
| ZANUBRUTINIB | 4 | ERBB2 |
| TUCATINIB | 4 | ERBB2 |
| TIRABRUTINIB | 4 | ERBB2 |
| PACLITAXEL | 4 | ERBB2 |
| LAZERTINIB | 4 | ERBB2 |
| HEXACHLOROPHENE | 4 | ERBB2 |
| DOXORUBICIN | 4 | ERBB2 |
| DASATINIB | 4 | ERBB2 |
| ERLOTINIB | 4 | ERBB2 |
Bioactivity and enzyme data
Enzyme cohort genes (≥1 EC): 1.
Cohort genes with ChEMBL bioactivity (full, sorted by assay count)
| Symbol | Assays | Type breakdown |
|---|---|---|
| ERBB2 | 1,221 | Binding:1136, Functional:79, ADMET:6 |
Cohort enzymes (BRENDA EC)
| Symbol | EC numbers | Names |
|---|---|---|
| ERBB2 | 2.7.10.1 | receptor protein-tyrosine kinase |
Cohort genes with high screening signal
≥100 ChEMBL assays — a studied-ness signal; see Therapeutics for approved-drug status.
| Symbol | ChEMBL assays |
|---|---|
| ERBB2 | 1,221 |
Pharmacogenomics
Cohort genes with a PharmGKB record: 1; with CPIC/DPWG dosing guidelines: 0.
No cohort gene has a CPIC/DPWG genotype-guided dosing guideline (PharmGKB).
Drug repurposing candidates
27 approved/phased drugs hit cohort targets but don’t yet appear in disease-level clinical trials. Target-inhibition rationale is strongest for cancer driver genes; a bioactivity hit is a screening signal, not a treatment claim.
| Compound | Max phase | Cohort target (bioactivity) |
|---|---|---|
| CLOTRIMAZOLE | 4 | ERBB2 |
| ERLOTINIB HYDROCHLORIDE | 4 | ERBB2 |
| PONATINIB | 4 | ERBB2 |
| AFATINIB | 4 | ERBB2 |
| LAPATINIB DITOSYLATE | 4 | ERBB2 |
| NERATINIB | 4 | ERBB2 |
| IBRUTINIB | 4 | ERBB2 |
| AFATINIB DIMALEATE | 4 | ERBB2 |
| CABOZANTINIB | 4 | ERBB2 |
| DACOMITINIB | 4 | ERBB2 |
| DACOMITINIB ANHYDROUS | 4 | ERBB2 |
| VANDETANIB | 4 | ERBB2 |
| TRIBROMSALAN | 4 | ERBB2 |
| BOSUTINIB | 4 | ERBB2 |
| BITHIONOL | 4 | ERBB2 |
| ASTEMIZOLE | 4 | ERBB2 |
| EBASTINE | 4 | ERBB2 |
| ACALABRUTINIB | 4 | ERBB2 |
| ZANUBRUTINIB | 4 | ERBB2 |
| TUCATINIB | 4 | ERBB2 |
| TIRABRUTINIB | 4 | ERBB2 |
| PACLITAXEL | 4 | ERBB2 |
| LAZERTINIB | 4 | ERBB2 |
| HEXACHLOROPHENE | 4 | ERBB2 |
| DOXORUBICIN | 4 | ERBB2 |
| DASATINIB | 4 | ERBB2 |
| ERLOTINIB | 4 | ERBB2 |
Druggability pyramid
Cohort genes binned by druggability tier (high → low):
| Tier | Definition | Genes | Symbols |
|---|---|---|---|
| A | Approved (phase 4 drug) | 1 | ERBB2 |
| 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: 252.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 84 |
| PHASE2 | 65 |
| PHASE1 | 54 |
| PHASE3 | 22 |
| PHASE1/PHASE2 | 14 |
| PHASE4 | 8 |
| EARLY_PHASE1 | 4 |
| PHASE2/PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT04475705 | PHASE4 | RECRUITING | Propofol vs Sevo for Paediatric Tumor Surgery |
| NCT04641819 | PHASE4 | ACTIVE_NOT_RECRUITING | Yangzheng Compound Mixture in the Treatment of Sleep Disorder in Cancer Patients |
| NCT00742222 | PHASE4 | COMPLETED | Electronic Xoft Intersociety Brachytherapy Trial: Electronic Brachytherapy (EBT) For Treatment of Early Stage Breast Cancer |
| NCT00847912 | PHASE4 | COMPLETED | CSP #562 - The VA Keratinocyte Carcinoma Chemoprevention Trial |
| NCT02151149 | PHASE4 | COMPLETED | Safety and Efficacy Study of Abraxane in Combination With Carboplatin to Treat Advanced NSCL Cancer in the Elderly |
| NCT04362072 | PHASE4 | COMPLETED | Study of Lorlatinib In People With ALK-positive Non-small Cell Lung Cancer |
| NCT04401059 | PHASE4 | UNKNOWN | Synergistic Effect of Elemene Plus TKIs Compared With TKIs in EGFR-mutated Advanced NSCLC:Prospective Study |
| NCT05848947 | PHASE4 | COMPLETED | SIR-Spheres Study to Calculate the Radiation-Absorbed Dose of 99mTc-MAA |
| NCT03091192 | PHASE3 | ACTIVE_NOT_RECRUITING | Savolitinib vs. Sunitinib in MET-driven PRCC. |
| NCT05261399 | PHASE3 | ACTIVE_NOT_RECRUITING | Savolitinib Plus Osimertinib Versus Platinum-based Doublet Chemotherapy in Participants With Non-Small Cell Lung Cancer Who Have Progressed on Osimertinib Treatment |
| NCT00034879 | PHASE3 | COMPLETED | Iressa Expanded Access Program (EAP) |
| NCT00126269 | PHASE3 | UNKNOWN | Trial Comparing Cisplatin With or Without Gemcitabine in Patients With Carcinoma of Unknown Primary |
| NCT00216372 | PHASE3 | COMPLETED | Efficacy and Safety of Lanreotide Microparticles as Palliative Treatment in Peritoneal Carcinomatosis |
| NCT00364455 | PHASE3 | COMPLETED | Impact of Erythropoietin Treatment Versus Placebo on Quality-of-life in Patients With Advanced Prostate Cancer. |
| NCT00532155 | PHASE3 | COMPLETED | A Study of Aflibercept Versus Placebo in Patients With Second-Line Docetaxel for Locally Advanced or Metastatic Non-Small-Cell Lung Cancer |
| NCT00822809 | PHASE3 | COMPLETED | CASIMAS: Catumaxomab Safety Phase IIIb Study With Intraperitoneal Infusion in Patients With Malignant Ascites Due to Epithelial Cancers |
| NCT00838201 | PHASE3 | COMPLETED | Extension Study to Evaluate Long Term Safety of Denosumab in Subjects Undergoing ADT for Non-Metastatic Prostate Cancer |
| NCT00863746 | PHASE3 | COMPLETED | A 3rd/4th Line Placebo-controlled Trial of Sorafenib in Patients With Predominantly Non Squamous Non-Small Cell Lung Cancer (NSCLC). |
| NCT00935675 | PHASE3 | UNKNOWN | Double-blind, Placebo-controlled, Randomized Study of the Effectiveness of Escitalopram on Emotional Distress of Head and Neck Cancer Patients During Cancer Treatment |
| NCT01009593 | PHASE3 | TERMINATED | Efficacy and Tolerability of ABT-869 Versus Sorafenib in Advanced Hepatocellular Carcinoma (HCC) |
| NCT01035229 | PHASE3 | COMPLETED | Global Study Looking at the Combination of RAD001 Plus Best Supportive Care (BSC) and Placebo Plus BSC to Treat Patients With Advanced Hepatocellular Carcinoma. |
| NCT01149161 | PHASE2/PHASE3 | UNKNOWN | Extent of Central Lymph Node Dissection in Papillary Thyroid Microcarcinoma |
| NCT01214343 | PHASE3 | UNKNOWN | Comparing Efficacy of Sorafenib Versus Sorafenib in Combination With Low-dose FP in Patients With Advanced HCC |
| NCT01345084 | PHASE3 | WITHDRAWN | Study Comparing Radiation Therapy and Chemotherapy With or Without Nimotuzumab |
| NCT02526953 | PHASE3 | UNKNOWN | Efficacy Study of Chemoradiotherapy With or Without Paclitaxel in Squamous-cell Anal Carcinoma Patients |
| NCT02539537 | PHASE3 | COMPLETED | A Randomized Phase III Trial Comparing Folfirinox to Gemcitabine in Locally Advanced Pancreatic Carcinoma |
| NCT02737501 | PHASE3 | COMPLETED | ALTA-1L Study: A Study of Brigatinib Versus Crizotinib in Anaplastic Lymphoma Kinase Positive (ALK+) Advanced Non-small Cell Lung Cancer (NSCLC) Participants |
| NCT03717038 | PHASE3 | WITHDRAWN | Sym004 Versus TAS-102 in Patients With mCRC |
| NCT03952403 | PHASE3 | UNKNOWN | A Study of HLX10 in Combination With Carboplatin Plus (+) Pemetrexed With or Without HLX04 Compared With Carboplatin+Pemetrexed in 1L Advanced Non-Squamous Non-Small Cell Lung Cancer (NSCLC) |
| NCT04006691 | PHASE3 | WITHDRAWN | Efficacy and Safety of UGN-101 in Recurrent Patients |
| NCT04222972 | PHASE3 | TERMINATED | A Study of Pralsetinib Versus Standard of Care for First-Line Treatment of Advanced Non-Small Cell Lung Cancer (NSCLC) |
| NCT03331601 | PHASE2 | RECRUITING | Evaluation of 68-GaNOTA-Anti-HER2 VHH1 Uptake in Brain Metastasis of Cancer Patients |
| NCT03708224 | PHASE2 | RECRUITING | Preoperative Immunotherapy in Patients With Squamous Cell Carcinoma of the Head and Neck |
| NCT03778229 | PHASE2 | ACTIVE_NOT_RECRUITING | Osimertinib Plus Savolitinib in EGFRm+/MET+ NSCLC Following Prior Osimertinib |
| NCT04787042 | PHASE1/PHASE2 | RECRUITING | Phase 1a and Phase 2 Study for Safety, Preliminary Efficacy, PK and PD of ST-067 |
| NCT04807166 | PHASE2 | ACTIVE_NOT_RECRUITING | Anlotinib Combined With Carboplatin/Paclitaxel as First-line Treatment in Patients With Advanced Ovarian Cancer |
| NCT05063916 | PHASE2 | ACTIVE_NOT_RECRUITING | Phase II Study of AK104 (Cadonilimab) for Recurrent Small Cell Neuroendocrine Carcinomas of the Cervix |
| NCT05283226 | PHASE2 | RECRUITING | Study to Evaluate the Safety and Efficacy of Oral NRC-2694-A in Combination With Paclitaxel in Patients With Recurrent and/or Metastatic Head and Neck Squamous Cell Carcinoma, Who Progressed on or After Immune Checkpoint Inhibitor Therapy |
| NCT05347212 | PHASE2 | ACTIVE_NOT_RECRUITING | Phase II Trial of Immunotherapy in Patients With Carcinomas Arising From the Renal Medulla |
| NCT05494060 | PHASE2 | RECRUITING | XELOX Combined With Anlotinib and Penpulimab vs XELOX as Adjuvant Therapy in ctDNA Positive Gastric and Esophagogastric Junction Adenocarcinoma |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| FLUOROURACIL | 4 | 7 |
| SORAFENIB | 4 | 4 |
| IRINOTECAN | 4 | 3 |
| BRIGATINIB | 4 | 2 |
| DOSTARLIMAB | 4 | 2 |
| MOGAMULIZUMAB | 4 | 2 |
| NIRAPARIB | 4 | 2 |
| OSIMERTINIB | 4 | 2 |
| PANITUMUMAB | 4 | 2 |
| PEMIGATINIB | 4 | 2 |
| PRALSETINIB | 4 | 2 |
| AFLIBERCEPT | 4 | 1 |
| BELINOSTAT | 4 | 1 |
| CAPMATINIB | 4 | 1 |
| CARBOPLATIN | 4 | 1 |
| CATUMAXOMAB | 4 | 1 |
| CRIZOTINIB | 4 | 1 |
| DENOSUMAB | 4 | 1 |
| ENSARTINIB | 4 | 1 |
| EPOETIN ALFA | 4 | 1 |
| FLUPHENAZINE DECANOATE | 4 | 1 |
| GEFITINIB | 4 | 1 |
| GEMCITABINE | 4 | 1 |
| INGENOL MEBUTATE | 4 | 1 |
| INTERFERON ALFA-2A | 4 | 1 |
| IXABEPILONE | 4 | 1 |
| KETOCONAZOLE | 4 | 1 |
| LEVOKETOCONAZOLE | 4 | 1 |
| LORLATINIB | 4 | 1 |
| MITOMYCIN | 4 | 1 |
Precision-medicine subtype map (CIViC)
Drug × molecular subtype: 1 predictive associations from 1 curated evidence items; also 1 oncogenic.
| Molecular subtype | Therapy | Effect | Level | CIViC |
|---|---|---|---|---|
| BAG4::FGFR1 Fusion | Fexagratinib | Sensitivity/Response | CIViC C | EID9243 |
Related Atlas pages
- Cohort genes: ERBB2
- Drugs: Fluorouracil, Sorafenib, Irinotecan, Brigatinib, Dostarlimab, Mogamulizumab, Niraparib, Osimertinib, Panitumumab, Pemigatinib, Pralsetinib, Aflibercept, Belinostat, Capmatinib, Carboplatin, Catumaxomab, Crizotinib, Denosumab, Ensartinib, Epoetin Alfa, Fluphenazine Decanoate, Gefitinib, Gemcitabine, Ingenol Mebutate, INTERFERON ALFA-2A, Ixabepilone, Ketoconazole, Levoketoconazole, Lorlatinib, Mitomycin