Thymic carcinoma
diseaseOn this page
Also known as carcinoma of thymusmalignant thymomaTHYCthymic carcinoma (excluding well differentiated thymic carcinoma)thymic carcinoma excluding well differentiated thymic carcinomathymoma type Cthymoma, malignantthymoma, malignant (morphologic abnormality)thymoma, type C (morphologic abnormality)thymus carcinomatype C thymoma
Summary
Thymic carcinoma (MONDO:0006451) is a cancer (an umbrella term covering 9 Mondo subtypes) with 1 cohort gene (1 CIViC-evidence somatic driver) and 47 clinical trials. Molecularly, KIT D820E confers sensitivity to Sorafenib in Thymic Carcinoma (CIViC Level C); 5 further subtype–drug associations are mapped below. Top therapeutic interventions include cyclophosphamide anhydrous, ramucirumab, and avelumab.
At a glance
- Classification: Cancer
- Prevalence: Unknown (Worldwide) [Orphanet-validated]
- Umbrella term: 9 Mondo subtypes
- Cohort genes: 1
- Phenotypes (HPO): 13
- Clinical trials: 47
- Precision-medicine evidence (CIViC): 6 subtype–drug associations
Clinical features
Signs & symptoms
Clinical features (HPO)
13 HPO clinical features (Orphanet curated; top 13 by frequency):
| HPO ID | Term | Frequency |
|---|---|---|
| HP:0100521 | Neoplasm of the thymus | Very frequent (80-99%) |
| HP:0100721 | Mediastinal lymphadenopathy | Very frequent (80-99%) |
| HP:0000969 | Edema | Frequent (30-79%) |
| HP:0002094 | Dyspnea | Frequent (30-79%) |
| HP:0005345 | Abnormal vena cava morphology | Frequent (30-79%) |
| HP:0006597 | Diaphragmatic paralysis | Frequent (30-79%) |
| HP:0012735 | Cough | Frequent (30-79%) |
| HP:0100540 | Palpebral edema | Frequent (30-79%) |
| HP:0100749 | Chest pain | Frequent (30-79%) |
| HP:0000975 | Hyperhidrosis | Occasional (5-29%) |
| HP:0001824 | Weight loss | Occasional (5-29%) |
| HP:0003473 | Fatigable weakness | Occasional (5-29%) |
| HP:0012378 | Fatigue | Occasional (5-29%) |
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | thymic carcinoma |
| Mondo ID | MONDO:0006451 |
| EFO | EFO:1000576 |
| Orphanet | 99868 |
| DOID | DOID:3284, DOID:4554 |
| ICD-11 | 1351671383 |
| NCIT | C7569, C7612 |
| SNOMED CT | 444374006 |
| UMLS | C0205969 |
| MedGen | 60049 |
| GARD | 0019695 |
| MedDRA | 10061031 |
| Anatomy (UBERON) | UBERON:0002370 |
| Is cancer (heuristic) | yes |
Also known as: carcinoma of thymus · malignant thymoma · THYC · thymic carcinoma · thymic carcinoma (excluding well differentiated thymic carcinoma) · thymic carcinoma excluding well differentiated thymic carcinoma · thymoma type C · thymoma, malignant · thymoma, malignant (morphologic abnormality) · thymoma, type C (morphologic abnormality) · thymus carcinoma · type C thymoma
Data availability: 4 cell lines.
Disease family
An umbrella term covering 9 Mondo subtypes.
Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › cancer › immune system cancer › thymus cancer › thymic carcinoma
Related subtypes (1): thymus lymphoma
Subtypes (9): invasive malignant thymoma, thymus gland adenocarcinoma, thymus squamous cell carcinoma, malignant type AB thymoma, lymphoepithelioma-like thymic carcinoma, thymus clear cell carcinoma, thymic sarcomatoid carcinoma, thymic undifferentiated carcinoma, thymic neuroendocrine 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: 18 · OMIM-shared: 0 · Dual-evidence (GWAS+Mendelian): 0
Somatic driver evidence (intOGen + CIViC, cohort fanout)
| Gene | intOGen role | Cancer types | CIViC |
|---|---|---|---|
| KIT | Act | AML,GIST,MEL,MGCT | CIViC #29 |
Orphanet rare-disease linkage (cohort genes)
| Gene | Orphanet ID | Rare disease |
|---|---|---|
| KIT | Orphanet:102724 | Acute myeloid leukemia with t(8;21)(q22;q22) translocation |
| KIT | Orphanet:158766 | Typical urticaria pigmentosa |
| KIT | Orphanet:158769 | Plaque-form urticaria pigmentosa |
| KIT | Orphanet:158772 | Nodular urticaria pigmentosa |
| KIT | Orphanet:158775 | Smoldering systemic mastocytosis |
| KIT | Orphanet:158778 | Isolated bone marrow mastocytosis |
| KIT | Orphanet:280785 | Bullous diffuse cutaneous mastocytosis |
| KIT | Orphanet:280794 | Pseudoxanthomatous diffuse cutaneous mastocytosis |
| KIT | Orphanet:2884 | Piebaldism |
| KIT | Orphanet:44890 | Gastrointestinal stromal tumor |
| KIT | Orphanet:566393 | Acute mast cell leukemia |
| KIT | Orphanet:566396 | Chronic mast cell leukemia |
| KIT | Orphanet:79455 | Cutaneous mastocytoma |
| KIT | Orphanet:842 | Testicular seminomatous germ cell tumor |
| KIT | Orphanet:90389 | Telangiectasia macularis eruptiva perstans |
| KIT | Orphanet:98829 | Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) |
| KIT | Orphanet:98834 | Acute myeloblastic leukemia with maturation |
| KIT | Orphanet:98849 | Systemic mastocytosis with associated hematologic neoplasm |
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 |
|---|---|---|---|---|---|
| KIT | HGNC:6342 | ENSG00000157404 | P10721 | Mast/stem cell growth factor receptor Kit | civic_evidence |
Cohort function summary
Lead sentence per gene, UniProt-curated.
| Symbol | Protein name | Function (lead sentence) |
|---|---|---|
| KIT | Mast/stem cell growth factor receptor Kit | Tyrosine-protein kinase that acts as a cell-surface receptor for the cytokine KITLG/SCF and plays an essential role in the regulation of cell survival and proliferation, hematopoiesis, stem cell maintenance, gametogenesis, mast cell develo… |
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) |
|---|---|---|---|---|
| KIT | Kinase | yes | 2.7.10.1 | Prot_kinase_dom, Ser-Thr/Tyr_kinase_cat_dom, Tyr_kinase_rcpt_3_CS |
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 |
|---|---|
| lateral nuclear group of thalamus | 1 |
| oocyte | 1 |
| secondary oocyte | 1 |
Per-gene tissue summary (top 30)
| Symbol | Bgee breadth | FANTOM5 breadth | SCXA | Top tissues |
|---|---|---|---|---|
| KIT | 263 | broad | marker | lateral nuclear group of thalamus, secondary oocyte, oocyte |
Protein interactions among cohort
Intra-cohort edges: 0.
Hub genes (top 10 by interactor count)
| Symbol | Interactor count |
|---|---|
| KIT | 6,087 |
Structural data
PDB: 1 · AlphaFold-only: 0 · No structure: 0
Cohort genes with PDB structures (top 30)
| Symbol | UniProt | PDB entries |
|---|---|---|
| KIT | P10721 | 52 |
Function
Pathway analysis
Distinct Reactome pathways touched by cohort: 39. 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 |
|---|---|---|---|---|
| Dasatinib-resistant KIT mutants | 1 | 11420.0× | 3e-04 | KIT |
| Imatinib-resistant KIT mutants | 1 | 11420.0× | 3e-04 | KIT |
| KIT mutants bind TKIs | 1 | 11420.0× | 3e-04 | KIT |
| Masitinib-resistant KIT mutants | 1 | 11420.0× | 3e-04 | KIT |
| Nilotinib-resistant KIT mutants | 1 | 11420.0× | 3e-04 | KIT |
| Regorafenib-resistant KIT mutants | 1 | 11420.0× | 3e-04 | KIT |
| Signaling by kinase domain mutants of KIT | 1 | 11420.0× | 3e-04 | KIT |
| Sunitinib-resistant KIT mutants | 1 | 11420.0× | 3e-04 | KIT |
| Signaling by juxtamembrane domain KIT mutants | 1 | 11420.0× | 3e-04 | KIT |
| Sorafenib-resistant KIT mutants | 1 | 11420.0× | 3e-04 | KIT |
| Drug resistance of KIT mutants | 1 | 11420.0× | 3e-04 | KIT |
| Signaling by extracellular domain mutants of KIT | 1 | 11420.0× | 3e-04 | KIT |
| Signaling by KIT in disease | 1 | 1142.0× | 0.003 | KIT |
| TFAP2 (AP-2) family regulates transcription of growth factors and their receptors | 1 | 761.3× | 0.004 | KIT |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 1 | 634.4× | 0.004 | KIT |
| Developmental Lineage of Mammary Gland Alveolar Cells | 1 | 634.4× | 0.004 | KIT |
| Regulation of KIT signaling | 1 | 601.0× | 0.004 | KIT |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | 1 | 519.1× | 0.004 | KIT |
| Developmental Lineage of Mammary Gland Luminal Epithelial Cells | 1 | 456.8× | 0.004 | KIT |
| PI3K/AKT Signaling in Cancer | 1 | 368.4× | 0.005 | KIT |
| Negative regulation of the PI3K/AKT network | 1 | 278.5× | 0.007 | KIT |
| Signaling by SCF-KIT | 1 | 248.3× | 0.007 | KIT |
| Transcriptional and post-translational regulation of MITF-M expression and activity | 1 | 178.4× | 0.010 | KIT |
| MAPK1/MAPK3 signaling | 1 | 131.3× | 0.012 | KIT |
| Constitutive Signaling by Aberrant PI3K in Cancer | 1 | 126.9× | 0.012 | KIT |
| MITF-M-regulated melanocyte development | 1 | 114.2× | 0.013 | KIT |
| MAPK family signaling cascades | 1 | 102.9× | 0.014 | KIT |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 1 | 96.8× | 0.014 | KIT |
| Intracellular signaling by second messengers | 1 | 91.4× | 0.015 | KIT |
| PIP3 activates AKT signaling | 1 | 66.8× | 0.019 | KIT |
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 |
|---|---|---|---|---|
| melanocyte adhesion | 1 | 16852.0× | 0.001 | KIT |
| positive regulation of pyloric antrum smooth muscle contraction | 1 | 16852.0× | 0.001 | KIT |
| positive regulation of colon smooth muscle contraction | 1 | 16852.0× | 0.001 | KIT |
| positive regulation of vascular associated smooth muscle cell differentiation | 1 | 8426.0× | 0.001 | KIT |
| Fc receptor signaling pathway | 1 | 5617.3× | 0.001 | KIT |
| Kit signaling pathway | 1 | 5617.3× | 0.001 | KIT |
| melanocyte migration | 1 | 5617.3× | 0.001 | KIT |
| obsolete regulation of bile acid metabolic process | 1 | 5617.3× | 0.001 | KIT |
| positive regulation of small intestine smooth muscle contraction | 1 | 5617.3× | 0.001 | KIT |
| mast cell chemotaxis | 1 | 4213.0× | 0.001 | KIT |
| hematopoietic stem cell migration | 1 | 4213.0× | 0.001 | KIT |
| mast cell differentiation | 1 | 4213.0× | 0.001 | KIT |
| positive regulation of dendritic cell cytokine production | 1 | 3370.4× | 0.001 | KIT |
| positive regulation of mast cell cytokine production | 1 | 3370.4× | 0.001 | KIT |
| mast cell proliferation | 1 | 3370.4× | 0.001 | KIT |
| positive regulation of mast cell proliferation | 1 | 3370.4× | 0.001 | KIT |
| lymphoid progenitor cell differentiation | 1 | 2808.7× | 0.001 | KIT |
| erythropoietin-mediated signaling pathway | 1 | 2808.7× | 0.001 | KIT |
| myeloid progenitor cell differentiation | 1 | 2407.4× | 0.001 | KIT |
| immature B cell differentiation | 1 | 2407.4× | 0.001 | KIT |
| glycosphingolipid metabolic process | 1 | 2407.4× | 0.001 | KIT |
| tongue development | 1 | 2106.5× | 0.001 | KIT |
| primordial germ cell migration | 1 | 1872.4× | 0.001 | KIT |
| positive regulation of long-term neuronal synaptic plasticity | 1 | 1872.4× | 0.001 | KIT |
| negative regulation of developmental process | 1 | 1872.4× | 0.001 | KIT |
| negative regulation of reproductive process | 1 | 1685.2× | 0.002 | KIT |
| positive regulation of pseudopodium assembly | 1 | 1296.3× | 0.002 | KIT |
| embryonic hemopoiesis | 1 | 991.3× | 0.003 | KIT |
| detection of mechanical stimulus involved in sensory perception of sound | 1 | 936.2× | 0.003 | KIT |
| ectopic germ cell programmed cell death | 1 | 842.6× | 0.003 | KIT |
Therapeutics
Drugs indicated for this disease
No approved or late-stage (phase ≥3) drug is indicated for this disease; the following are in earlier-phase trials only.
Earlier-phase candidates (phase 2, investigational — efficacy not yet established): Amrubicin, Avelumab, Belinostat, Carboplatin, Cisplatin, Epacadostat, Erfonrilimab, Lenvatinib, Paclitaxel, Pembrolizumab, Ramucirumab, Sacituzumab Govitecan, Sunitinib.
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 |
|---|---|
| KIT | PONATINIB |
Top cohort targets by molecule count
| Symbol | Molecules | Max phase |
|---|---|---|
| KIT | 99 | 4 |
Drugs targeting cohort genes (top 30)
| Molecule | Max phase | Targets in cohort |
|---|---|---|
| PONATINIB | 4 | KIT |
| FEDRATINIB | 4 | KIT |
| TIVOZANIB | 4 | KIT |
| LENVATINIB | 4 | KIT |
| AXITINIB | 4 | KIT |
| SORAFENIB | 4 | KIT |
| DASATINIB ANHYDROUS | 4 | KIT |
| NICLOSAMIDE | 4 | KIT |
| IMATINIB MESYLATE | 4 | KIT |
| RUXOLITINIB | 4 | KIT |
| INFIGRATINIB PHOSPHATE | 4 | KIT |
| INFIGRATINIB | 4 | KIT |
| REGORAFENIB | 4 | KIT |
| ENTRECTINIB | 4 | KIT |
| CABOZANTINIB | 4 | KIT |
| CERITINIB | 4 | KIT |
| VANDETANIB | 4 | KIT |
| NILOTINIB | 4 | KIT |
| BOSUTINIB | 4 | KIT |
| BRIGATINIB | 4 | KIT |
| PEXIDARTINIB | 4 | KIT |
| AVAPRITINIB | 4 | KIT |
| RIPRETINIB | 4 | KIT |
| PAZOPANIB | 4 | KIT |
| NINTEDANIB | 4 | KIT |
| SUNITINIB | 4 | KIT |
| DASATINIB | 4 | KIT |
| ERLOTINIB | 4 | KIT |
| QUIZARTINIB | 4 | KIT |
| CRIZOTINIB | 4 | KIT |
Bioactivity and enzyme data
Enzyme cohort genes (≥1 EC): 1.
Cohort genes with ChEMBL bioactivity (full, sorted by assay count)
| Symbol | Assays | Type breakdown |
|---|---|---|
| KIT | 2,305 | Binding:2242, ADMET:32, Functional:22, Toxicity:9 |
Cohort enzymes (BRENDA EC)
| Symbol | EC numbers | Names |
|---|---|---|
| KIT | 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 |
|---|---|
| KIT | 2,305 |
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
28 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) |
|---|---|---|
| PONATINIB | 4 | KIT |
| FEDRATINIB | 4 | KIT |
| TIVOZANIB | 4 | KIT |
| LENVATINIB | 4 | KIT |
| AXITINIB | 4 | KIT |
| SORAFENIB | 4 | KIT |
| DASATINIB ANHYDROUS | 4 | KIT |
| NICLOSAMIDE | 4 | KIT |
| IMATINIB MESYLATE | 4 | KIT |
| RUXOLITINIB | 4 | KIT |
| INFIGRATINIB PHOSPHATE | 4 | KIT |
| INFIGRATINIB | 4 | KIT |
| ENTRECTINIB | 4 | KIT |
| CABOZANTINIB | 4 | KIT |
| CERITINIB | 4 | KIT |
| VANDETANIB | 4 | KIT |
| NILOTINIB | 4 | KIT |
| BOSUTINIB | 4 | KIT |
| BRIGATINIB | 4 | KIT |
| PEXIDARTINIB | 4 | KIT |
| AVAPRITINIB | 4 | KIT |
| RIPRETINIB | 4 | KIT |
| PAZOPANIB | 4 | KIT |
| NINTEDANIB | 4 | KIT |
| DASATINIB | 4 | KIT |
| ERLOTINIB | 4 | KIT |
| QUIZARTINIB | 4 | KIT |
| CRIZOTINIB | 4 | KIT |
Druggability pyramid
Cohort genes binned by druggability tier (high → low):
| Tier | Definition | Genes | Symbols |
|---|---|---|---|
| A | Approved (phase 4 drug) | 1 | KIT |
| 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: 47.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| PHASE2 | 29 |
| Not specified | 8 |
| PHASE1 | 6 |
| PHASE1/PHASE2 | 3 |
| PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT06402708 | PHASE3 | RECRUITING | Postoperative Adjuvant Chemotherapy for Thymic Cancer (FUSCC-Thymic 3) |
| NCT01025089 | PHASE2 | ACTIVE_NOT_RECRUITING | Chemotherapy Plus Cetuximab Followed by Surgical Resection in Patients With Locally Advanced or Recurrent Thymoma or Thymic Carcinoma |
| NCT03076554 | PHASE2 | ACTIVE_NOT_RECRUITING | A Pilot Study to Investigate the Safety and Clinical Activity of Avelumab (MSB0010718C) in Thymoma and Thymic Carcinoma After Progression on Platinum-Based Chemotherapy |
| NCT03134118 | PHASE2 | ACTIVE_NOT_RECRUITING | Nivolumab in Patients With Type B3 Thymoma and Thymic Carcinoma (NIVOTHYM) |
| NCT03463460 | PHASE2 | ACTIVE_NOT_RECRUITING | Pembrolizumab and Sunitinib Malate in Treating Participants With Refractory Metastatic or Unresectable Thymic Cancer |
| NCT06019468 | PHASE2 | RECRUITING | Neoadjuvant Treatment For Locally Advanced Thymic Cancer |
| NCT06248515 | PHASE2 | RECRUITING | A Phase II Trial of Sacituzumab Govitecan in Patients With Advanced Thymic Epithelial Tumors |
| NCT06838910 | PHASE2 | RECRUITING | Tislelizumab Combined With Anlotinib as Second-line Therapy in Thymoma and Thymic Carcinoma |
| NCT06980077 | PHASE2 | RECRUITING | Ivonescimab for the Treatment of Thymic Cancer |
| NCT07324629 | PHASE2 | NOT_YET_RECRUITING | Sacituzumab Tirumotecan in Participants With Locally Advanced or Metastatic Thymic Carcinoma |
| NCT07479628 | PHASE2 | NOT_YET_RECRUITING | Neoadjuvant Adebrelimab Plus CRT for Locally Advanced Thymic Carcinoma |
| NCT07598955 | PHASE1/PHASE2 | RECRUITING | Target-Selected CAR-NK Cells (CD30, CD5, or Mesothelin) for Relapsed/Refractory B2 Thymoma or Thymic Carcinoma |
| NCT00003662 | PHASE2 | COMPLETED | Umbilical Cord Blood Transplantation in Treating Patients With Hematologic Cancer or Other Hematologic or Metabolic Diseases |
| NCT00010257 | PHASE2 | COMPLETED | Carboplatin Combined With Paclitaxel in Treating Patients With Advanced Thymoma |
| NCT00198133 | PHASE2 | COMPLETED | Phase II Study of Alimta (Pemetrexed) Treatment of Advanced Thymoma and Thymic Carcinoma |
| NCT00589290 | PHASE2 | COMPLETED | Belinostat (PXD101) to Treat Tumors of the Thymus at an Advanced Stage |
| NCT00818090 | PHASE2 | TERMINATED | Paclitaxel and Cisplatin for Thymic Neoplasm |
| NCT00965250 | PHASE2 | COMPLETED | Multicenter Phase II Study of IMC-A12 in Patients With Thymoma and Thymic Carcinoma Who Have Been Previously Treated With Chemotherapy |
| NCT01011439 | PHASE2 | TERMINATED | Phase II Study Of Oral PHA-848125AC In Patients With Thymic Carcinoma |
| NCT01100944 | PHASE1/PHASE2 | TERMINATED | A Phase 1/2 Study of PXD101 (Belinostat) in Combination With Cisplatin, Doxorubicin and Cyclophosphamide in the First Line Treatment of Advanced or Recurrent Thymic, Malignancies |
| NCT01301391 | PHASE2 | TERMINATED | Study Of Oral PHA-848125AC In Patients With Malignant Thymoma Previously Treated With Multiple Lines Of Chemotherapy |
| NCT01364727 | PHASE2 | COMPLETED | A Phase 2 Study of Amrubicin in Relapsed or Refractory Thymic Malignancies |
| NCT02062632 | PHASE2 | TERMINATED | Doxepin Hydrochloride in Treating Esophageal Pain in Patients With Thoracic Cancer Receiving Radiation Therapy to the Thorax With or Without Chemotherapy |
| NCT02307500 | PHASE2 | COMPLETED | Regorafenib in Patients With Metastatic Solid Tumors Who Have Progressed After Standard Therapy |
| NCT02364076 | PHASE2 | UNKNOWN | Pembrolizumab and Epacadostat in Patients With Thymic Carcinoma |
| NCT02623127 | PHASE2 | COMPLETED | A Study of Sunitinib in Patients With Metastatic or Recurrent Thymic Carcinoma |
| NCT03449173 | PHASE2 | UNKNOWN | Trial of Sunitinib in Patients With Type B3 Thymoma or Thymic Carcinoma in Second and Further Lines (Style Trial) |
| NCT03583086 | PHASE1/PHASE2 | COMPLETED | Phase I/II Eval Safety & Prelim Activity Nivolumab Comb W/Vorolanib Pts W/Refractory Thoracic Tumors |
| NCT03694002 | PHASE2 | COMPLETED | Carboplatin and Paclitaxel With or Without Ramucirumab in Treating Patients With Locally Advanced, Recurrent, or Metastatic Thymic Cancer That Cannot Be Removed by Surgery |
| NCT03921671 | PHASE2 | UNKNOWN | Ramucirumab and Carbo-Paclitaxel for Untreated Thymic Carcinoma / B3 Thymoma With Carcinoma (RELEVENT) |
| NCT04469725 | PHASE2 | TERMINATED | KN046 (a Humanized PD-L1/CTLA4 Bispecific Single Domain Fc Fusion Protein Antibody) in Subjects With Thymic Carcinoma |
| NCT04710628 | PHASE2 | COMPLETED | Combination of Pembrolizumab and Lenvatinib, in Pre-treated Thymic CArcinoma paTIents |
| NCT04925947 | PHASE2 | TERMINATED | A Study of KN046 in Patients With Thymic Carcinoma Who Failed Immune Checkpoint Inhibitors |
| NCT07118176 | PHASE1 | RECRUITING | Determining the Biodistribution of an Imaging Tracer (68Ga-FAPi-46) in Patients With Solid Tumors or Hematologic Cancers |
| NCT07181720 | PHASE1 | RECRUITING | CD70-Targeted CAR-T Therapy in CD70-Positive Advanced Solid Tumors |
| NCT00314873 | PHASE1 | COMPLETED | Pilot Study of Imatinib (Gleevec) as Treatment for Advanced Thymic Carcinoma |
| NCT01143545 | PHASE1 | TERMINATED | Pilot Study of Allogeneic Tumor Cell Vaccine With Metronomic Oral Cyclophosphamide and Celecoxib in Patients Undergoing Resection of Lung and Esophageal Cancers, Thymic Neoplasms, and Malignant Pleural Mesotheliomas |
| NCT03517488 | PHASE1 | COMPLETED | A Study of XmAb®20717 in Subjects With Selected Advanced Solid Tumors |
| NCT04430842 | PHASE1 | COMPLETED | Dose Escalation Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of QBS10072S |
| NCT01385722 | Not specified | ENROLLING_BY_INVITATION | Molecular Analysis of Thoracic Malignancies |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| CYCLOPHOSPHAMIDE ANHYDROUS | 4 | 4 |
| RAMUCIRUMAB | 4 | 2 |
| AVELUMAB | 4 | 1 |
| BELINOSTAT | 4 | 1 |
| BUSULFAN | 4 | 1 |
| DOXEPIN HYDROCHLORIDE | 4 | 1 |
| REGORAFENIB | 4 | 1 |
| SACITUZUMAB GOVITECAN | 4 | 1 |
| SUNITINIB | 4 | 1 |
| ERFONRILIMAB | 3 | 2 |
| AMRUBICIN | 3 | 1 |
| EPACADOSTAT | 3 | 1 |
| IVONESCIMAB | 3 | 1 |
| SACITUZUMAB TIRUMOTECAN | 3 | 1 |
| FAPI-46 GA-68 | 2 | 1 |
| RIMIDUCID | 2 | 1 |
| VOROLANIB | 2 | 1 |
| VUDALIMAB | 2 | 1 |
| MILCICLIB MALEATE | 1 | 2 |
| CHEMBL1200462 | 0 | 1 |
Precision-medicine subtype map (CIViC)
Drug × molecular subtype: 6 predictive associations from 6 curated evidence items.
| Molecular subtype | Therapy | Effect | Level | CIViC |
|---|---|---|---|---|
| KIT D820E | Sorafenib | Sensitivity/Response | CIViC C | EID7356 |
| KIT P577_D579DEL | Sorafenib | Sensitivity/Response | CIViC C | EID7360 |
| KIT V559G | Imatinib Mesylate | Sensitivity/Response | CIViC C | EID7357 |
| KIT V560DEL | Imatinib | Sensitivity/Response | CIViC C | EID486 |
| KIT V560DEL | Imatinib Mesylate | Sensitivity/Response | CIViC C | EID7359 |
| KIT Y553N | Imatinib Mesylate | Sensitivity/Response | CIViC C | EID7358 |
Related Atlas pages
- Cohort genes: KIT
- Drugs: Cyclophosphamide, Ramucirumab, Avelumab, Belinostat, Busulfan, Doxepin, Regorafenib, Sacituzumab Govitecan, Sunitinib, Erfonrilimab, Amrubicin, Epacadostat, Ivonescimab, Sacituzumab Tirumotecan, Sorafenib, Imatinib