thymoma type B3
disease diseaseOn this page
Also known as atypical thymomaepithelial malignant thymomaepithelial thymomamalignant thymoma type B3squamoid thymomawell differentiated thymic carcinomawell-differentiated thymic carcinoma
Summary
thymoma type B3 (MONDO:0006458) is a disease and 3 clinical trials. Top therapeutic interventions include regorafenib. A subtype of thymoma type B — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 3
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | thymoma type B3 |
| Mondo ID | MONDO:0006458 |
| EFO | EFO:1000583 |
| DOID | DOID:7926 |
| NCIT | C7997 |
| UMLS | C0279705 |
| MedGen | 124648 |
| GARD | 0024417 |
| Is cancer (heuristic) | no |
Also known as: atypical thymoma · epithelial malignant thymoma · epithelial thymoma · malignant thymoma type B3 · squamoid thymoma · thymoma type B3 · well differentiated thymic carcinoma · well-differentiated thymic carcinoma
Disease family
This is a subtype of thymoma type B. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.
Classification path: disease › human disease › disease by body system or component › immune system disorder › leukocyte disorder › thymoma type B › thymoma type B3
Related subtypes (2): cortical thymoma, thymoma type B1
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
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 3.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| PHASE2 | 3 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT03134118 | PHASE2 | ACTIVE_NOT_RECRUITING | Nivolumab in Patients With Type B3 Thymoma and Thymic Carcinoma (NIVOTHYM) |
| NCT02307500 | PHASE2 | COMPLETED | Regorafenib in Patients With Metastatic Solid Tumors Who Have Progressed After Standard Therapy |
| NCT04710628 | PHASE2 | COMPLETED | Combination of Pembrolizumab and Lenvatinib, in Pre-treated Thymic CArcinoma paTIents |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| REGORAFENIB | 4 | 1 |
Related Atlas pages
- Drugs: Regorafenib