Adult intracranial malignant hemangiopericytoma

disease
On this page

Also known as adult intracranial anaplastic hemangiopericytomaadult intracranial solitary fibrous tumor/hemangiopericytoma, grade 3adult malignant intracranial hemangiopericytomacentral nervous system solitary fibrous tumor/hemangiopericytoma, grade 3malignant adult intracranial hemangiopericytoma

Summary

Adult intracranial malignant hemangiopericytoma (MONDO:0003857) is a disease and 2 clinical trials. Top therapeutic interventions include gadobenate dimeglumine, gadobutrol, and gadopentetate dimeglumine. A subtype of hemangiopericytoma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 2

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameadult intracranial malignant hemangiopericytoma
Mondo IDMONDO:0003857
DOIDDOID:6333
NCITC9183
UMLSC1334558
MedGen235288
GARD0027653
Is cancer (heuristic)no

Also known as: adult intracranial anaplastic hemangiopericytoma · adult intracranial solitary fibrous tumor/hemangiopericytoma, grade 3 · adult malignant intracranial hemangiopericytoma · central nervous system solitary fibrous tumor/hemangiopericytoma, grade 3 · malignant adult intracranial hemangiopericytoma

Disease family

This is a subtype of hemangiopericytoma. 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 syndromeneoplasmmesenchymal cell neoplasm › pericytic neoplasm › hemangiopericytic tumor › hemangiopericytomaadult intracranial malignant hemangiopericytoma

Related subtypes (7): kidney hemangiopericytoma, meninges hemangiopericytoma, breast hemangiopericytoma, retroperitoneal hemangiopericytoma, heart malignant hemangiopericytoma, hemangiopericytoma, malignant, hemangiopericytoma of skin

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: 2.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE11
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01119599PHASE1COMPLETEDRO4929097, Temozolomide, and Radiation Therapy in Treating Patients With Newly Diagnosed Malignant Glioma
NCT02967380Not specifiedTERMINATEDGadobutrol Versus Gadopentetate Dimeglumine or Gadobenate Dimeglumine Before DCE-MRI in Diagnosing Patients With Multiple Sclerosis, Grade II-IV Glioma, or Brain Metastases

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
GADOBENATE DIMEGLUMINE41
GADOBUTROL41
GADOPENTETATE DIMEGLUMINE41
CHEMBL422879401