Columnar cell variant thyroid gland papillary carcinoma

disease
On 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

FieldValue
Canonical namecolumnar cell variant thyroid gland papillary carcinoma
Mondo IDMONDO:0004102
DOIDDOID:7088
NCITC35830
UMLSC1333120
MedGen272499
GARD0023823
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 tumorneoplastic disease or syndromeneoplasmcancercarcinomaadenocarcinomapapillary adenocarcinomathyroid gland papillary carcinomacolumnar 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)

PhaseTrials
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT02973997PHASE2COMPLETEDLenvatinib and Pembrolizumab in Differentiated Thyroid Cancers (DTC)

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
LENVATINIB42