T-cell prolymphocytic leukemia

disease
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Also known as chronic T-cell leukaemiachronic T-cell leukemiachronic T-cell lymphocytic leukaemiachronic T-cell lymphocytic leukemiaCLL, T-cellleukemia, T-cell, chronicT cell chronic lymphocytic leukaemiaT cell chronic lymphocytic leukemiaT cell CLLT cell prolymphocytic leukaemiaT cell prolymphocytic leukemiaT prolymphocytic leukaemiaT prolymphocytic leukemiaT-cell chronic lymphocytic leukaemiaT-cell chronic lymphocytic leukemiaT-cell CLLT-PLLTPLL

Summary

T-cell prolymphocytic leukemia (MONDO:0019468) is a cancer with 1 cohort gene (1 CIViC-evidence somatic driver; 4 ClinVar predisposition records) and 26 clinical trials. Top therapeutic interventions include fludarabine phosphate, duvelisib, and carmustine.

At a glance

  • Classification: Cancer
  • Prevalence: Unknown (Worldwide) [Orphanet-validated]
  • Cohort genes: 1
  • ClinVar variants: 4
  • Clinical trials: 26

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameT-cell prolymphocytic leukemia
Mondo IDMONDO:0019468
EFOEFO:1000560
MeSHD015461
Orphanet86871
DOIDDOID:0081042
ICD-11352523899
NCITC4752
SNOMED CT277545003, 277567002
UMLSC2363142
MedGen391707
GARD0013731
MedDRA10042985
Is cancer (heuristic)yes

Also known as: chronic T-cell leukaemia · chronic T-cell leukemia · chronic T-cell lymphocytic leukaemia · chronic T-cell lymphocytic leukemia · CLL, T-cell · leukemia, T-cell, chronic · T cell chronic lymphocytic leukaemia · T cell chronic lymphocytic leukemia · T cell CLL · T cell prolymphocytic leukaemia · T cell prolymphocytic leukemia · T prolymphocytic leukaemia · T prolymphocytic leukemia · T-cell chronic lymphocytic leukaemia · T-cell chronic lymphocytic leukemia · T-cell CLL · T-cell prolymphocytic leukemia · T-PLL · TPLL

Data availability: 4 ClinVar variants · 4 cell lines.

Disease family

Classification path: 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-cellsmature T-cell and NK-cell non-Hodgkin lymphomaT-cell prolymphocytic leukemia

Related subtypes (7): angioimmunoblastic T-cell lymphoma, systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood, hydroa vacciniforme-like lymphoma, T-cell large granular lymphocyte leukemia, aggressive NK-cell leukemia, anaplastic large cell lymphoma, breast implant-associated anaplastic large cell lymphoma

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

ClinVar germline variants

4 retrieved; paginated sample, class counts are floors:

2 pathogenic, 1 pathogenic/likely pathogenic, 1 uncertain significance

ClinVarVariant (HGVS)GeneClassificationReview
3019NM_000051.4(ATM):c.7638_7646del (p.Arg2547_Ser2549del)ATMPathogenic/Likely pathogeniccriteria provided, multiple submitters, no conflicts
3023NM_000051.4(ATM):c.7271T>G (p.Val2424Gly)ATMPathogenicreviewed by expert panel
3042NM_000051.4(ATM):c.5309C>G (p.Ser1770Ter)ATMPathogeniccriteria provided, multiple submitters, no conflicts
3026NM_000051.4(ATM):c.5044G>C (p.Asp1682His)ATMUncertain significancecriteria provided, single submitter

Genes & proteins

Mendelian disease overlap and somatic drivers

GenCC: 0 · Orphanet: 8 · OMIM-shared: 0 · Dual-evidence (GWAS+Mendelian): 0

Somatic driver evidence (intOGen + CIViC, cohort fanout)

GeneintOGen roleCancer typesCIViC
ATMLoFBLCA,BRCA,CCRCC,CHOL,CLLSLL,COAD,COADREAD,ESCA,HCC,LUAD,LUSC,MEL,NSCLC,PAAD,PANCREAS,PANET,PCM,PLMESO,PRAD,PROSTATE,STAD,UCEC,UTUC,WDTCCIViC #69

Orphanet rare-disease linkage (cohort genes)

GeneOrphanet IDRare disease
ATMOrphanet:100Ataxia-telangiectasia
ATMOrphanet:1331Familial prostate cancer
ATMOrphanet:145Hereditary breast and/or ovarian cancer syndrome
ATMOrphanet:227535Hereditary breast cancer
ATMOrphanet:370109Ataxia-telangiectasia variant
ATMOrphanet:440437Familial colorectal cancer Type X
ATMOrphanet:52416Mantle cell lymphoma
ATMOrphanet:67038B-cell chronic lymphocytic leukemia

Cohort genes → proteins

1 cohort genes, 1 distinct canonical proteins.

Evidence partition

SubsetGenes
multi_evidence1

Cohort genes (full)

SymbolHGNCEnsemblUniProtNameEvidence
ATMHGNC:795ENSG00000149311Q13315Serine-protein kinase ATMclinvar

Cohort function summary

Lead sentence per gene, UniProt-curated.

SymbolProtein nameFunction (lead sentence)
ATMSerine-protein kinase ATMSerine/threonine protein kinase which activates checkpoint signaling upon double strand breaks (DSBs), apoptosis and genotoxic stresses such as ionizing ultraviolet A light (UVA), thereby acting as a DNA damage sensor.

Protein-family classification

Druggable: 1 · Difficult: 0 · Unknown: 0 · Druggable fraction: 1.0

Family distribution

Cohort families vs a genome-wide background (hypergeometric, BH-FDR; fold = observed/expected). Counts kept; sorted by enrichment, so the catch-all Other/Unknown bucket no longer leads.

FamilyGenesFoldFDR
Kinase127.7×0.036

Per-gene assignment

SymbolFamilyDruggable?ECInterPro (top 3)
ATMKinaseyes2.7.11.1PI3/4_kinase_cat_dom, PIK-rel_kinase_FAT, FATC_dom

Expression context

Cohort genes with no expression data: 0.

1 cohort gene are a single-cell marker in ≥1 SCXA experiment.

Breadth distribution (Bgee present_calls)

BucketGenes
narrow (1-5 tissues)0
moderate (6-20)0
broad (>20)1
unknown0

Top tissues across cohort

TissueCohort genes
calcaneal tendon1
colonic epithelium1
corpus callosum1

Per-gene tissue summary (top 30)

SymbolBgee breadthFANTOM5 breadthSCXATop tissues
ATM286ubiquitousmarkercalcaneal tendon, colonic epithelium, corpus callosum

Protein interactions among cohort

Intra-cohort edges: 0.

Hub genes (top 10 by interactor count)

SymbolInteractor count
ATM7,383

Structural data

PDB: 1 · AlphaFold-only: 0 · No structure: 0

Cohort genes with PDB structures (top 30)

SymbolUniProtPDB entries
ATMQ1331514

Function

Pathway analysis

Distinct Reactome pathways touched by cohort: 61. Enrichment computed across 1 evidence-associated genes (1 with Reactome annotation).

Pathways by enrichment

Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.

PathwayCohort genesFoldFDRSample cohort genes
Sensing of DNA Double Strand Breaks11903.3×0.007ATM
TP53 Regulates Transcription of Caspase Activators and Caspases1951.7×0.007ATM
Pexophagy1951.7×0.007ATM
Defective homologous recombination repair (HRR) due to PALB2 loss of function1951.7×0.007ATM
Diseases of DNA Double-Strand Break Repair1815.7×0.007ATM
Defective homologous recombination repair (HRR) due to BRCA2 loss of function1815.7×0.007ATM
Stabilization of p531761.3×0.007ATM
p53-Dependent G1 DNA Damage Response1713.8×0.007ATM
p53-Dependent G1/S DNA damage checkpoint1713.8×0.007ATM
G1/S DNA Damage Checkpoints1671.8×0.007ATM
Resolution of D-Loop Structures1634.4×0.007ATM
Diseases of DNA repair1571.0×0.007ATM
TP53 Regulates Transcription of Cell Death Genes1543.8×0.007ATM
TP53 Regulates Transcription of Genes Involved in Cytochrome C Release1543.8×0.007ATM
Regulation of TP53 Activity through Methylation1543.8×0.007ATM
Regulation of TP53 Expression and Degradation1519.1×0.007ATM
DNA Double Strand Break Response1475.8×0.007ATM
Impaired BRCA2 binding to PALB21456.8×0.007ATM
Defective homologous recombination repair (HRR) due to BRCA1 loss of function1423.0×0.007ATM
Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function1423.0×0.007ATM
Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function1423.0×0.007ATM
Cellular response to heat stress1393.8×0.007ATM
Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA)1393.8×0.007ATM
Homologous DNA Pairing and Strand Exchange1380.7×0.007ATM
Homology Directed Repair1308.6×0.007ATM
HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA)1308.6×0.007ATM
Impaired BRCA2 binding to RAD511308.6×0.007ATM
Resolution of D-loop Structures through Holliday Junction Intermediates1300.5×0.007ATM
HDR through Single Strand Annealing (SSA)1292.8×0.007ATM
Regulation of TP53 Degradation1292.8×0.007ATM

GO biological processes by enrichment

Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.

GO termCohort genesFoldFDRSample cohort genes
establishment of RNA localization to telomere18426.0×0.002ATM
establishment of protein-containing complex localization to telomere18426.0×0.002ATM
positive regulation of telomerase catalytic core complex assembly18426.0×0.002ATM
pre-B cell allelic exclusion15617.3×0.002ATM
cellular response to nitrosative stress15617.3×0.002ATM
peptidyl-serine autophosphorylation13370.4×0.003ATM
negative regulation of telomere capping13370.4×0.003ATM
regulation of telomere maintenance via telomerase12808.7×0.003ATM
positive regulation of telomere maintenance via telomere lengthening12808.7×0.003ATM
lipoprotein catabolic process12407.4×0.003ATM
V(D)J recombination12106.5×0.003ATM
meiotic telomere clustering11872.4×0.003ATM
female meiotic nuclear division11685.2×0.003ATM
histone mRNA catabolic process11685.2×0.003ATM
cellular response to X-ray11685.2×0.003ATM
DNA double-strand break processing11532.0×0.003ATM
regulation of autophagosome assembly11123.5×0.003ATM
pexophagy11053.2×0.003ATM
regulation of cellular response to heat11053.2×0.003ATM
positive regulation of DNA damage response, signal transduction by p53 class mediator1991.3×0.003ATM
replicative senescence1991.3×0.003ATM
negative regulation of B cell proliferation1936.2×0.003ATM
oocyte development1936.2×0.003ATM
cellular response to stress1842.6×0.003ATM
signal transduction in response to DNA damage1802.5×0.003ATM
positive regulation of telomere maintenance via telomerase1732.7×0.004ATM
cellular response to gamma radiation1601.9×0.004ATM
mitotic spindle assembly checkpoint signaling1561.7×0.004ATM
reciprocal meiotic recombination1561.7×0.004ATM
male meiotic nuclear division1543.6×0.004ATM

Therapeutics

Drugs indicated for this disease

No approved or late-stage (phase ≥3) drug is indicated for this disease; the following are in earlier-phase trials only.

Earlier-phase candidates (phase 2, investigational — efficacy not yet established): Cyclosporine, Fludarabine Phosphate, Ibrutinib, Mycophenolate Mofetil, Venetoclax.

Drug target analysis

Approved (phase 4): 1 · Phase ≥3: 1 · Phased (≥1): 1 · Undrugged: 0

Druggability breadth: 1 of 1 evidence-associated genes (100%) have a ChEMBL target (buckets above are over the deeply-mined display cohort).

Genes with an approved drug

The molecule shown is one approved compound that hits the gene — not necessarily a drug of choice or one indicated for this disease.

SymbolExample approved molecule
ATMAMIODARONE HYDROCHLORIDE

Top cohort targets by molecule count

SymbolMoleculesMax phase
ATM354

Drugs targeting cohort genes (top 30)

MoleculeMax phaseTargets in cohort
AMIODARONE HYDROCHLORIDE4ATM
FURAZOLIDONE4ATM
ESTRADIOL ACETATE4ATM
NAFTIFINE HYDROCHLORIDE4ATM
METHYSERGIDE MALEATE4ATM
AMITRIPTYLINE HYDROCHLORIDE4ATM
XYLOMETAZOLINE HYDROCHLORIDE4ATM
FLUVOXAMINE MALEATE4ATM
ESTRADIOL VALERATE4ATM
PERMETHRIN4ATM
MITOTANE4ATM
TICLOPIDINE HYDROCHLORIDE4ATM
ENOXIMONE4ATM
METHYLENE BLUE ANHYDROUS4ATM
DITHIAZANINE IODIDE4ATM
ETHACRYNIC ACID4ATM
SECNIDAZOLE4ATM
MENADIONE4ATM
FENOFIBRATE4ATM
DIPYRIDAMOLE4ATM
DACTOLISIB3ATM
STREPTONIGRIN2ATM
CALCIMYCIN2ATM
ENPIROLINE2ATM
OXACEPROL2ATM
TOLONIUM CHLORIDE2ATM
ESTRADIOL BENZOATE2ATM
BERZOSERTIB2ATM
LARTESERTIB2ATM
ALTHIAZIDE2ATM

Bioactivity and enzyme data

Enzyme cohort genes (≥1 EC): 1.

Cohort genes with ChEMBL bioactivity (full, sorted by assay count)

SymbolAssaysType breakdown
ATM240Binding:233, Functional:5, ADMET:2

Cohort enzymes (BRENDA EC)

SymbolEC numbersNames
ATM2.7.11.1non-specific serine/threonine protein kinase

Cohort genes with high screening signal

≥100 ChEMBL assays — a studied-ness signal; see Therapeutics for approved-drug status.

SymbolChEMBL assays
ATM240

Pharmacogenomics

Cohort genes with a PharmGKB record: 1; with CPIC/DPWG dosing guidelines: 0.

No cohort gene has a CPIC/DPWG genotype-guided dosing guideline (PharmGKB).

Drug repurposing candidates

30 approved/phased drugs hit cohort targets but don’t yet appear in disease-level clinical trials. Target-inhibition rationale is strongest for cancer driver genes; a bioactivity hit is a screening signal, not a treatment claim.

CompoundMax phaseCohort target (bioactivity)
AMIODARONE HYDROCHLORIDE4ATM
FURAZOLIDONE4ATM
ESTRADIOL ACETATE4ATM
NAFTIFINE HYDROCHLORIDE4ATM
METHYSERGIDE MALEATE4ATM
AMITRIPTYLINE HYDROCHLORIDE4ATM
XYLOMETAZOLINE HYDROCHLORIDE4ATM
FLUVOXAMINE MALEATE4ATM
ESTRADIOL VALERATE4ATM
PERMETHRIN4ATM
MITOTANE4ATM
TICLOPIDINE HYDROCHLORIDE4ATM
ENOXIMONE4ATM
METHYLENE BLUE ANHYDROUS4ATM
DITHIAZANINE IODIDE4ATM
ETHACRYNIC ACID4ATM
SECNIDAZOLE4ATM
MENADIONE4ATM
FENOFIBRATE4ATM
DIPYRIDAMOLE4ATM
DACTOLISIB3ATM
STREPTONIGRIN2ATM
CALCIMYCIN2ATM
ENPIROLINE2ATM
OXACEPROL2ATM
TOLONIUM CHLORIDE2ATM
ESTRADIOL BENZOATE2ATM
BERZOSERTIB2ATM
LARTESERTIB2ATM
ALTHIAZIDE2ATM

Druggability pyramid

Cohort genes binned by druggability tier (high → low):

TierDefinitionGenesSymbols
AApproved (phase 4 drug)1ATM
BPhased (≥1) drug, not yet approved0
CDruggable family + PDB, no drug0
DDruggable family + AlphaFold only, no drug0
EDifficult family or no structure, no drug0

Undrugged target profiles

0 cohort genes are undrugged. Ranked by ‘starting-point quality’ (assay depth + drugged-partner adjacency).

Clinical trials & evidence

Clinical trials

Clinical trials: 26.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE111
PHASE28
PHASE1/PHASE25
PHASE31
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01231412PHASE3COMPLETEDGraft-Versus-Host Disease Prophylaxis in Treating Patients With Hematologic Malignancies Undergoing Unrelated Donor Peripheral Blood Stem Cell Transplant
NCT04496349PHASE2RECRUITINGA Study Evaluating APG-115 as a Single Agent or in Combination With APG-2575 in Subjects With R/R T-PLL and NHL
NCT06420076PHASE1/PHASE2RECRUITINGSequential CAR-T Cells Therapy for CD5/CD7 Positive T-cell Acute Lymphoblastic Leukemia and Lymphoblastic Lymphoma Using CD5/CD7-Specific CAR-T Cells
NCT06810778PHASE1/PHASE2RECRUITINGDuvelisib and Venetoclax in Patients With Relapsed or Refractory Peripheral T-cell Lymphoma (PTCL)
NCT07311746PHASE1/PHASE2NOT_YET_RECRUITINGPhase Ib/II Trial of Cladribine/Ruxolitinib/Venetoclax in Patients With Relapsed/Refractory T-cell Prolymphocytic Leukemia
NCT07356245PHASE2RECRUITINGRuxolitinib Maintenance Post-Hematopoietic Stem Cell Transplant T-Cell Lymphoma
NCT00005803PHASE1/PHASE2COMPLETEDAutologous Stem Cell Transplant Followed by Donor Stem Cell Transplant in Treating Patients With Relapsed or Refractory Lymphoma
NCT00060424PHASE2COMPLETEDFludarabine Phosphate and Total-Body Irradiation Before Donor Peripheral Blood Stem Cell Transplant in Treating Patients With Chronic Lymphocytic Leukemia or Small Lymphocytic Leukemia
NCT01008462PHASE2COMPLETEDAutologous Peripheral Blood Stem Cell Transplant Followed by Donor Bone Marrow Transplant in Treating Patients With High-Risk Hodgkin Lymphoma, Non-Hodgkin Lymphoma, Multiple Myeloma, or Chronic Lymphocytic Leukemia
NCT01186640PHASE2COMPLETEDCombined Immunochemotherapy in Patients With T-Prolymphocytic Leukemia (T-PLL)
NCT01251575PHASE2COMPLETEDSirolimus, Cyclosporine, and Mycophenolate Mofetil in Preventing Graft-versus-Host Disease in Treating Patients With Blood Cancer Undergoing Donor Peripheral Blood Stem Cell Transplant
NCT02742727PHASE1/PHASE2UNKNOWNCAR-pNK Cell Immunotherapy in CD7 Positive Leukemia and Lymphoma
NCT03873493PHASE2COMPLETEDA Study Evaluating the Efficacy of Venetoclax Plus Ibrutinib in Participants With T-cell Prolymphocytic Leukemia
NCT04312841PHASE2COMPLETEDLetermovir for the Prevention of Cytomegalovirus Reactivation in Patients With Hematological Malignancies Treated With Alemtuzumab
NCT04771572PHASE1RECRUITINGStudy of Oral Administration of LP-118 in Patients With Relapsed or Refractory CLL, SLL, MDS, MDS/MPN, AML, CMML-2, MPN-BP, ALL, MF, NHL, RT, MM or T-PLL.
NCT05010005PHASE1RECRUITINGA Study of Ruxolitinib and Duvelisib in People With Lymphoma
NCT05377827PHASE1ACTIVE_NOT_RECRUITINGDose-Escalation and Dose-Expansion Study to Evaluate the Safety and Tolerability of Anti-CD7 Allogeneic CAR T-Cells (WU-CART-007) in Patients With CD7+ Hematologic Malignancies
NCT05823571PHASE1ACTIVE_NOT_RECRUITINGItacitinib With High-dose Posttransplantation Cyclophosphamide in Older Patients
NCT00749502PHASE1COMPLETEDA Study of MK4827 in Participants With Advanced Solid Tumors or Hematologic Malignancies (MK-4827-001 AM8)
NCT02512497PHASE1COMPLETEDRomidepsin Maintenance After Allogeneic Stem Cell Transplantation
NCT02689453PHASE1COMPLETEDSubcutaneous Recombinant Human IL-15 (s.c. rhIL-15) and Alemtuzumab for People With Refractory or Relapsed Chronic and Acute Adult T-cell Leukemia (ATL)
NCT03989466PHASE1COMPLETEDItacitinib and Alemtuzumab in Treating Patients With T-Cell Prolymphocytic Leukemia
NCT04526795PHASE1TERMINATEDFludarabine, Cytarabine, and Pegcrisantaspase for the Treament of Relapsed or Refractory Leukemia
NCT04823091PHASE1UNKNOWNAnti-CD7 CAR-Engineered T Cells for T Lymphoid Malignancies Malignancies
NCT05225584PHASE1COMPLETEDSafety, PK, PD, Clinical Activity of KT-333 in Adult Patients With Refractory Lymphoma, Large Granular Lymphocytic Leukemia, Solid Tumors
NCT05978141Not specifiedRECRUITINGA Registry for People With T-cell Lymphoma

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
FLUDARABINE PHOSPHATE48
DUVELISIB42
CARMUSTINE41
CLADRIBINE41
LETERMOVIR41
NIRAPARIB41
ROMIDEPSIN41
ITACITINIB32
APG-257521
INTERLEUKIN 15, RECOMBINANT NON-GLYCOSYLATED21
CHEMBL380534802
CHEMBL453868402
CHEMBL40635201
CHEMBL478965601
CHEMBL477688101
CHEMBL406646501