Giant cell tumor
diseaseOn this page
Also known as giant cell neoplasmgiant cell tumor (morphologic abnormality)giant cell tumor (qualifier value)giant cell tumor NOS (morphologic abnormality)giant cell tumors (morphologic abnormality)giant cell tumour (morphologic abnormality)giant cell tumour (qualifier value)giant cell tumour NOS (morphologic abnormality)giant cell tumoursgiant cell tumours (morphologic abnormality)tumor of the giant celltumour of the giant cell
Summary
Giant cell tumor (MONDO:0002171) is a cancer and 5 clinical trials. Top therapeutic interventions include denosumab. A subtype of neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Classification: Cancer
- Clinical trials: 5
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | giant cell tumor |
| Mondo ID | MONDO:0002171 |
| MeSH | D005870 |
| DOID | DOID:200 |
| NCIT | C3055 |
| SNOMED CT | 443790001 |
| UMLS | C0017525 |
| MedGen | 6598 |
| Is cancer (heuristic) | yes |
Also known as: giant cell neoplasm · giant cell tumor · giant cell tumor (morphologic abnormality) · giant cell tumor (qualifier value) · giant cell tumor NOS (morphologic abnormality) · giant cell tumors (morphologic abnormality) · giant cell tumour (morphologic abnormality) · giant cell tumour (qualifier value) · giant cell tumour NOS (morphologic abnormality) · giant cell tumours · giant cell tumours (morphologic abnormality) · tumor of the giant cell · tumour of the giant cell
Disease family
This is a subtype of neoplasm. 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 etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › giant cell tumor
Related subtypes (47): pre-malignant neoplasm, endocrine gland neoplasm, hematopoietic and lymphoid system neoplasm, skin neoplasm, mesenchymal cell neoplasm, epidural spinal canal neoplasm, skeletal muscle neoplasm, trophoblastic neoplasm, cancer, germ cell tumor, benign neoplasm, upper aerodigestive tract neoplasm, histiocytoma, embryonal neoplasm, head and neck neoplasm, epithelial neoplasm, reproductive system neoplasm, non-seminomatous lesion, odontogenic cyst, phosphaturic mesenchymal tumor, thyroglossal duct cyst, hamartoma, mesenchymoma, mesothelial neoplasm, peritoneal neoplasm, virus associated tumor, nail tumor, respiratory tract neoplasm, spindle cell neoplasm, mixed neoplasm, urinary system neoplasm, cystic neoplasm, childhood neoplasm, melanocytic neoplasm, digestive system neoplasm, nervous system neoplasm, neoplasm of thorax, connective tissue neoplasm, bronchial adenomas/carcinoids childhood, diffuse idiopathic pulmonary neuroendocrine cell hyperplasia, erythroplakia, retroperitoneal neoplasm, cardiovascular neoplasm, dermoid or epidermoid cyst of the central nervous system, connective and soft tissue neoplasm, NTRK fusion positive cancer, RET fusion positive cancer
Subtypes (2): malignant giant cell tumor, tenosynovial giant cell tumor
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
Drugs indicated for this disease
1 approved, 1 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.
| Drug | Development status |
|---|---|
| Denosumab | Approved (phase 4) |
| Narlumosbart | Phase 3 (in late-stage trials) |
Earlier-phase candidates (phase 2, investigational — efficacy not yet established): Calcium.
Clinical trials & evidence
Clinical trials
Clinical trials: 5.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 4 |
| PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00680992 | PHASE2 | COMPLETED | Study of Denosumab in Subjects With Giant Cell Tumor of Bone |
| NCT05463796 | Not specified | RECRUITING | InAdvance: Surveillance, Prevention, and Interception in a Population at Risk for Cancer |
| NCT02948088 | Not specified | COMPLETED | Tenosynovial Giant Cell Tumors (TGCT) Observational Platform Project |
| NCT05542524 | Not specified | COMPLETED | Oral Care of Patients Treated With Anti-RANK-ligand Antibodies for a Giant Cell Tumour |
| NCT06331104 | Not specified | COMPLETED | Network Pharmacology Prediction: Mechanism Study of Puerarin in the Treatment of Giant Cell Tumors of Bone |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| DENOSUMAB | 4 | 1 |
Related Atlas pages
- Drugs: Denosumab