neoplasm of mature T-cells or NK-cells

disease
On this page

Also known as mature T and NK neoplasmsmature T-cell and NK-cell neoplasmmature T-cell neoplasm

Summary

neoplasm of mature T-cells or NK-cells (MONDO:0005169) is a cancer and 2 clinical trials. Top therapeutic interventions include copanlisib, gemcitabine, and nelfinavir mesylate. A subtype of T-cell and NK-cell neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Classification: Cancer
  • Clinical trials: 2

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameneoplasm of mature T-cells or NK-cells
Mondo IDMONDO:0005169
EFOEFO:0002426
NCITC27909
UMLSC1334640
MedGen233675
GARD0024159
Is cancer (heuristic)yes

Also known as: mature T and NK neoplasms · mature T-cell and NK-cell neoplasm · mature T-cell neoplasm

Disease family

An umbrella term covering 4 Mondo subtypes.

Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumorneoplastic disease or syndromeneoplasmhematopoietic and lymphoid system neoplasmhematopoietic and lymphoid cell neoplasmlymphoid neoplasm › T-cell and NK-cell neoplasm › neoplasm of mature T-cells or NK-cells

Related subtypes (1): T lymphoblastic leukemia/lymphoma

Subtypes (4): mature T-cell and NK-cell non-Hodgkin lymphoma, chronic lymphoproliferative disorder of NK-cells, peripheral T-cell lymphoma, not otherwise specified, EBV-positive T-cell lymphoproliferative disorder 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: 2.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE1/PHASE21
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03052933PHASE1/PHASE2COMPLETEDCopanlisib and Gemcitabine in Relapsed/Refractory PTCL
NCT01164709PHASE1COMPLETEDNelfinavir Mesylate and Bortezomib in Treating Patients With Relapsed or Progressive Advanced Hematologic Cancer

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
COPANLISIB41
GEMCITABINE41
NELFINAVIR MESYLATE41
CHEMBL36544201