Columnar cell variant thyroid gland papillary carcinoma
diseaseOn this page
Also known as columnar cell variant papillary carcinomacolumnar cell variant papillary thyroid gland carcinoma
Summary
Columnar cell variant thyroid gland papillary carcinoma (MONDO:0004102) is a cancer and 1 clinical trial. Top therapeutic interventions include lenvatinib. A subtype of thyroid gland papillary carcinoma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Classification: Cancer
- Clinical trials: 1
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | columnar cell variant thyroid gland papillary carcinoma |
| Mondo ID | MONDO:0004102 |
| DOID | DOID:7088 |
| NCIT | C35830 |
| UMLS | C1333120 |
| MedGen | 272499 |
| GARD | 0023823 |
| Is cancer (heuristic) | yes |
Also known as: columnar cell variant papillary carcinoma · columnar cell variant papillary thyroid gland carcinoma · columnar cell variant thyroid gland papillary carcinoma
Disease family
This is a subtype of thyroid gland papillary carcinoma. 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: human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › cancer › carcinoma › adenocarcinoma › papillary adenocarcinoma › thyroid gland papillary carcinoma › columnar cell variant thyroid gland papillary carcinoma
Related subtypes (5): thyroid gland diffuse sclerosing papillary carcinoma, multicentric papillary thyroid carcinoma, tall cell variant thyroid gland papillary carcinoma, thyroid gland papillary and follicular carcinoma, thyroid cancer, nonmedullary, 1
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: 1.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT02973997 | PHASE2 | COMPLETED | Lenvatinib and Pembrolizumab in Differentiated Thyroid Cancers (DTC) |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| LENVATINIB | 4 | 2 |
Related Atlas pages
- Drugs: Lenvatinib