Sweat gland cancer

disease
On this page

Also known as cancer of sweat glandmalignant neoplasm of sweat glandmalignant neoplasm of the sweat glandmalignant sweat gland neoplasmmalignant tumor of sweat glandmalignant tumor of the sweat glandmalignant tumour of sweat glandmalignant tumour of the sweat glandsweat gland neoplasms, malignant

Summary

Sweat gland cancer (MONDO:0002206) is a cancer and 1 clinical trial. Top therapeutic interventions include nivolumab and talimogene laherparepvec. A subtype of sweat gland neoplasm — 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 namesweat gland cancer
Mondo IDMONDO:0002206
DOIDDOID:2095
NCITC4810
UMLSC1321904
MedGen231171
Anatomy (UBERON)UBERON:0001820
Is cancer (heuristic)yes

Also known as: cancer of sweat gland · malignant neoplasm of sweat gland · malignant neoplasm of the sweat gland · malignant sweat gland neoplasm · malignant tumor of sweat gland · malignant tumor of the sweat gland · malignant tumour of sweat gland · malignant tumour of the sweat gland · sweat gland cancer · sweat gland neoplasms, malignant

Disease family

This is a subtype of sweat gland 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 tumorneoplastic disease or syndromeneoplasmskin neoplasmepidermal appendage tumorsweat gland neoplasmsweat gland cancer

Related subtypes (5): eccrine sweat gland neoplasm, syringoma, apocrine sweat gland neoplasm, sweat gland adenoma, benign neoplasm of sweat gland

Subtypes (4): apocrine sweat gland cancer, malignant syringoma, eccrine sweat gland cancer, sweat gland 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

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
NCT02978625PHASE2ACTIVE_NOT_RECRUITINGTalimogene Laherparepvec and Nivolumab in Treating Patients With Refractory Lymphomas or Advanced or Refractory Non-melanoma Skin Cancers

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
NIVOLUMAB41
TALIMOGENE LAHERPAREPVEC41