Refractory hematologic cancer

disease
On this page

Also known as refractory hematologic malignancy

Summary

Refractory hematologic cancer (MONDO:0004111) is a cancer (an umbrella term covering 6 Mondo subtypes) and 9 clinical trials. Top therapeutic interventions include dacomitinib anhydrous, acalabrutinib, and cobimetinib. A subtype of hematopoietic and lymphoid cell neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Classification: Cancer
  • Umbrella term: 6 Mondo subtypes
  • Clinical trials: 9

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namerefractory hematologic cancer
Mondo IDMONDO:0004111
DOIDDOID:712
NCITC27357
UMLSC1335724
MedGen233400
GARD0023831
Is cancer (heuristic)yes

Also known as: refractory hematologic cancer · refractory hematologic malignancy

Disease family

This is a subtype of hematopoietic and lymphoid cell 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 syndromeneoplasmhematopoietic and lymphoid system neoplasmhematopoietic and lymphoid cell neoplasmrefractory hematologic cancer

Related subtypes (7): central nervous system hematopoietic neoplasm, leukemia, lymphoid neoplasm, myeloid neoplasm, histiocytic and dendritic cell neoplasm, myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2, myelodysplastic syndrome with excess blasts

Subtypes (6): refractory hairy cell leukemia, refractory precursor T-lymphoblastic lymphoma/leukemia, refractory plasma cell neoplasm, refractory anemia with excess blasts in transformation, myelodysplastic syndrome with multilineage dysplasia, refractory cytopenia of childhood

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: 9.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE1/PHASE23
PHASE22
PHASE12
Not specified2

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03328078PHASE1/PHASE2RECRUITINGCA-4948-101: Open-Label, Dose Escalation and Expansion Trial of Emavusertib (CA-4948) in Relapsed or Refractory Primary Central Nervous System Lymphoma (R/R PCNSL)
NCT00838890PHASE1/PHASE2TERMINATEDA Study of BMS-863233 in Patients With Hematologic Cancer
NCT03739606PHASE2WITHDRAWNFlotetuzumab in Treating Patients With Recurrent or Refractory CD123 Positive Blood Cancer
NCT03882203PHASE2COMPLETEDCLAGE Sequential With Flu-Bu Conditioning for Refractory Acute Leukemia
NCT05205252PHASE1/PHASE2WITHDRAWNA Study of Tazemetostat in Combination With Various Treatments in Participants With Blood Cancer.
NCT03878524PHASE1TERMINATEDSerial Measurements of Molecular and Architectural Responses to Therapy (SMMART) PRIME Trial
NCT04681105PHASE1COMPLETEDFlotetuzumab for the Treatment of Relapsed or Refractory Advanced CD123-Positive Hematological Malignancies
NCT05270096Not specifiedRECRUITINGInternational Leukemia Target Board
NCT05713214Not specifiedRECRUITINGLong-term Follow-up After Adoptive Transfer of Genetically Modified Cell Products

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
DACOMITINIB ANHYDROUS43
ACALABRUTINIB41
COBIMETINIB41
COPANLISIB41
DAROLUTAMIDE41
ENASIDENIB41
ENTRECTINIB41
HYALURONIDASE (HUMAN RECOMBINANT)41
IBRUTINIB41
IDELALISIB41
LORLATINIB41
MOSUNETUZUMAB41
NERATINIB41
OLAPARIB41
PONATINIB41
RANITIDINE41
TAFASITAMAB41
TAZEMETOSTAT41
VISMODEGIB41
EMAVUSERTIB21
FLOTETUZUMAB21
CHEMBL474750601
CHEMBL518755401
CHEMBL527692501
CHEMBL539843101
CHEMBL117108601
CHEMBL34422701
CHEMBL409500801
CHEMBL430315501
CHEMBL443640601