Sarcomatoid mesothelioma

disease
On this page

Also known as malignant fibrous mesothelioma (morphologic abnormality)sarcomatoid mesothelioma (morphologic abnormality)

Summary

Sarcomatoid mesothelioma (MONDO:0006407) is a disease and 3 clinical trials. Top therapeutic interventions include cisplatin, cediranib maleate, and tivantinib. A subtype of malignant mesothelioma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 3

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namesarcomatoid mesothelioma
Mondo IDMONDO:0006407
EFOEFO:1000521
DOIDDOID:4488
NCITC45655
UMLSC0334513
MedGen137774
GARD0024401
Is cancer (heuristic)no

Also known as: malignant fibrous mesothelioma (morphologic abnormality) · sarcomatoid mesothelioma · sarcomatoid mesothelioma (morphologic abnormality)

Disease family

This is a subtype of malignant mesothelioma. 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 syndromeneoplasmcancermalignant mesotheliomasarcomatoid mesothelioma

Related subtypes (10): ovarian malignant mesothelioma, malignant pericardial mesothelioma, malignant pleural mesothelioma, malignant peritoneal mesothelioma, malignant epithelioid mesothelioma, malignant biphasic mesothelioma, localized pleural mesothelioma, diffused pleural mesothelioma, pleural mesothelioma in situ, mesothelioma of the tunica vaginalis

Subtypes (2): lymphohistiocytoid mesothelioma, pleural sarcomatoid mesothelioma

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: 3.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE22
PHASE1/PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01064648PHASE1/PHASE2ACTIVE_NOT_RECRUITINGPemetrexed Disodium and Cisplatin With or Without Cediranib Maleate in Treating Patients With Malignant Pleural Mesothelioma
NCT01861301PHASE2TERMINATEDTivantinib in Treating Patients With Previously Treated Malignant Mesothelioma
NCT02399371PHASE2COMPLETEDPembrolizumab in Treating Patients With Malignant Mesothelioma

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
CISPLATIN41
CEDIRANIB MALEATE31
TIVANTINIB31
CHEMBL447537901
CHEMBL478573401