Metastatic malignant neoplasm in the spinal cord

disease
On this page

Also known as metastasis to spinal cordMetastatic malignant neoplasm to the spinal cordMetastatic neoplasm to the spinal cordMetastatic tumor to the spinal cordMetastatic tumour to the spinal cordSecondary malignant neoplasm to the spinal cordSecondary malignant tumor to the spinal cordSecondary malignant tumour to the spinal cord

Summary

Metastatic malignant neoplasm in the spinal cord (MONDO:0044912) is a cancer and 1 clinical trial. Top therapeutic interventions include doxepin hydrochloride. A subtype of spinal cord cancer — 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 namemetastatic malignant neoplasm in the spinal cord
Mondo IDMONDO:0044912
NCITC4585
SNOMED CT94600009
UMLSC0347016
MedGen138075
GARD0027980
Anatomy (UBERON)UBERON:0002240
Is cancer (heuristic)yes

Also known as: metastasis to spinal cord · Metastatic malignant neoplasm in the spinal cord · Metastatic malignant neoplasm to the spinal cord · Metastatic neoplasm to the spinal cord · Metastatic tumor to the spinal cord · Metastatic tumour to the spinal cord · Secondary malignant neoplasm to the spinal cord · Secondary malignant tumor to the spinal cord · Secondary malignant tumour to the spinal cord

Disease family

This is a subtype of spinal cord cancer. 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 syndromeneoplasmcancernervous system cancercentral nervous system cancerspinal cord cancermetastatic malignant neoplasm in the spinal cord

Related subtypes (7): spinal cord lymphoma, spinal cord melanoma, spinal cord sarcoma, spinal cord glioma, spinal cord neuroblastoma, spinal meninges cancer, spinal cord primitive neuroectodermal 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

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
NCT02062632PHASE2TERMINATEDDoxepin Hydrochloride in Treating Esophageal Pain in Patients With Thoracic Cancer Receiving Radiation Therapy to the Thorax With or Without Chemotherapy

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
DOXEPIN HYDROCHLORIDE41
CHEMBL120046201