Disease Briefing

Acute lymphoblastic leukemia: research and therapeutic landscape

A live synthesis of what is being targeted, what is being trialled, which datasets exist, and where the actionable gaps sit — assembled from public APIs, with every figure traceable to its source.

Generated 2026-09-12Sources Open Targets · ClinicalTrials.gov · openFDA · GEO · PubMed · Europe PMC · iCite · RePORTERRanked 629 studies · 39,025 GEO samples
Reading as
Reorders emphasis only — nothing is hidden or loaded on demand.

Answer block

12 genes recurrently implicated in acute lymphoblastic leukemia — CD19, CD22, ABL1, IKZF1, CDKN2A, NOTCH1, KMT2A, ETV6, PAX5, CRLF2, JAK2, TP53 — triaged for what can actually be aimed at them, alongside the trials, public datasets, literature and funding around the disease. Every figure below carries its source and retrieval date in the section it comes from.

17
drugs carry an FDA label naming acute lymphoblastic leukemia: Asparaginase Erwinia Chrysanthemi (Recombinant)-Rywn, Blinatumomab, Brexucabtagene Autoleucel, Calaspargase Pegol, Clofarabine, Dasatinib and 11 more. This counts labels, not treatment — the disease is also treated with agents approved under broader indications
3
of the 12 genes above carry a drug that is approved in acute lymphoblastic leukemia itself — ABL1, CD19, CD22. Across all of them 95 drug entries reach these genes, 83 distinct once salt forms are merged
131
registered CD19 cell-therapy trials in acute lymphoblastic leukemia, 59 active and 10 withdrawn. Counted from ClinicalTrials.gov across 9 synonyms, deduplicated by NCT id, interventional studies only — the query is published in the JSON beside this page so the number can be re-derived
4
targets carry an Open Targets tractability signal and have no clinical programme of any kind: IKZF1, NOTCH1, ETV6, PAX5. CD19, CD22, ABL1 all have cell-therapy trials, so they are undrugged rather than untouched
2,016
human GEO series match the disease; 629 survive on-topic filtering, and only 32 are patient cohorts of 100+ samples
68
Europe PMC full-text papers name GSE11877 — the highest accession-mention count in the set. A mention is not proof of reanalysis, so read it as reach rather than reuse
$33.2M
NIH obligations in FY2025, up 86% since 2013 — while distinct core projects went 51 to 67. Both more projects (+31%) and larger awards, the latter carrying more of the growth; core projects are not the same unit as laboratories

Target landscape

Open Targets · retrieved 2026-09-12 · weekly

12 genes recurrently implicated in acute lymphoblastic leukemia, triaged for whether anything can actually be aimed at them. The zeros are the informative rows.

Of 12 recurrently implicated genes, 7 carry any drug at all. That is a statement about these 12 gene targets, not about the disease: Acute lymphoblastic leukemia does have labelled therapy — 17 drugs, listed in the next section.

Two different questions

The table below asks what can be aimed at 12 recurrently implicated genes. That is narrower than what is approved for the disease, and narrower again than what acute lymphoblastic leukemia is actually treated with, which includes agents approved under broader indications. All three are on this page and they are kept apart deliberately.

GeneDrugsApproval, and whether it reached this diseaseOpen Targets tractabilitycomputed from protein features and literature — a signal that a modality is worth trying, not evidence that it worksCell therapy here
CD19 across cancers → 14 9 approvedAxicabtagene Ciloleucel, Blinatumomab, Brexucabtagene Autoleucel, Inebilizumab, Lisocabtagene Maraleucel, Loncastuximab Tesirine, Obecabtagene Autoleucel, Tafasitamab, TisagenlecleucelApproved in acute lymphoblastic leukemia: Blinatumomab, Brexucabtagene Autoleucel, Obecabtagene Autoleucel, Tisagenlecleucel.118 active of 172 acute lymphoblastic leukemia trials antibody, other clinical modality, protein degrader 59 active of 131 trials
CD22 across cancers → 11 2 approvedInotuzumab Ozogamicin, Moxetumomab PasudotoxApproved in acute lymphoblastic leukemia: Inotuzumab Ozogamicin.64 active of 135 acute lymphoblastic leukemia trials antibody, other clinical modality, protein degrader, small molecule 33 active of 68 trials
ABL1 across cancers → 21 9 approvedAsciminib, Bosutinib, Dasatinib, Imatinib, Nilotinib, Nilotinib Hydrochloride, Ponatinib, Regorafenib, UmbralisibApproved in acute lymphoblastic leukemia: Dasatinib, Imatinib, Ponatinib.75 active of 268 acute lymphoblastic leukemia trials antibody, protein degrader, small molecule 2 active of 4 trials
IKZF1 across cancers → 0 No drug protein degrader, small molecule
CDKN2A across cancers → 0 No drug
NOTCH1 across cancers → 1 Phase 1BrontictuzumabNo acute lymphoblastic leukemia trial of any of these drugs antibody, protein degrader, small molecule
KMT2A across cancers → 2 Phase 3Revumenib, Revumenib Sesquifumarate6 active of 8 acute lymphoblastic leukemia trials protein degrader, small molecule
ETV6 0 No drug antibody, protein degrader, small molecule
PAX5 0 No drug protein degrader, small molecule
CRLF2 0 No drug
JAK2 across cancers → 26 13 approvedBaricitinib, Delgocitinib, Deuruxolitinib, Fedratinib, Filgotinib, Lestaurtinib, Momelotinib, Momelotinib Dihydrochloride, Pacritinib, Ruxolitinib, Tofacitinib, Upadacitinib, Upadacitinib HemihydrateApproved in juvenile idiopathic arthritis, atopic eczema, rheumatoid arthritis and 16 other indications. No acute lymphoblastic leukemia indication appears on these drugs’ labels.15 active of 36 acute lymphoblastic leukemia trials antibody, protein degrader, small molecule
TP53 across cancers → 8 Phase 3Alrizomadlin, Cenersen, Contusugene Ladenovec, Eprenetapopt, Idasanutlin, Navtemadlin, Siremadlin, Teprasiran1 trials, none active other clinical modality, protein degrader, small molecule

Dataset evidence counts studies in the 629-study ranked set whose title or abstract names the gene; the bar is scaled to NOTCH1. Sources: Open Targets Platform and NCBI GEO, retrieved 2026-09-12. Clinical stage is the highest reached for any indication — see the per-drug indications noted in each row. Target-prioritisation reference only; not clinical or prescribing guidance.

What is actually approved here

openFDA drug labels · weekly

17 drugs carry an FDA label naming acute lymphoblastic leukemia: Asparaginase Erwinia Chrysanthemi (Recombinant)-Rywn, Blinatumomab, Brexucabtagene Autoleucel, Calaspargase Pegol, Clofarabine, Dasatinib, Daunorubicin, Imatinib, Imatinib Oral, Inotuzumab Ozogamicin, Mercaptopurine, Nelarabine, Obecabtagene Autoleucel, Pegaspargase, Ponatinib, Sargramostim, Tisagenlecleucel. Separately, 25 of the drugs returned for the genes in the table above are approved only for other diseases and reach acute lymphoblastic leukemia through trials, not through their labels.

17Labelled for acute lymphoblastic leukemiaFDA INDICATIONS AND USAGE names the disease
25Approved, but for another diseasereturned for the genes in the table above
3Backbone agents listing itbroad cytotoxics whose labels name many tumours
59Active CD19 cell-therapy trialsof 131 registered

Every label that names acute lymphoblastic leukemia

DrugRoleWhat the label says
Asparaginase Erwinia Chrysanthemi (Recombinant)-RywnRylazeLabelled hereRYLAZE is indicated as a component of a multi-agent chemotherapeutic regimen for the treatment of acute lymphoblastic leukemia (ALL) and lymphoblastic lymphoma (LBL) in adult and pediatric patients 1 month or older who have developed hypersensitivity to E. coli -derived asparaginase.
BlinatumomabBLINCYTOLabelled hereRelapsed or refractory CD19-positive B-cell precursor acute lymphoblastic leukemia (ALL).
Brexucabtagene AutoleucelTECARTUSLabelled hereAcute Lymphoblastic Leukemia TECARTUS is indicated for the treatment of adult patients with relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL).
Calaspargase PegolasparlasLabelled hereAcute Lymphoblastic Leukemia ASPARLAS is indicated as a component of a multi-agent chemotherapeutic regimen for the treatment of acute lymphoblastic leukemia in pediatric and young adult patients age 1 month to 21 years.
ClofarabineCLOFARABINE, ClofarabineLabelled hereClofarabine injection is indicated for the treatment of pediatric patients 1 to 21 years old with relapsed or refractory acute lymphoblastic leukemia after at least two prior regimens.
DasatinibDASATINIB, Dasatinib, PHYRAGOLabelled herePhiladelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) with resistance or intolerance to prior therapy.
DaunorubicinDaunorubicin Hydrochloride, daunorubicin hydrochlorideLabelled hereDaunorubicin hydrochloride in combination with other approved anticancer drugs is indicated for remission induction in acute nonlymphocytic leukemia (myelogenous, monocytic, erythroid) of adults and for remission induction in acute lymphocytic leukemia of children and adults.
ImatinibGleevec, IMATINIB MESYLATE, ImatinibLabelled hereAdult Patients With Ph+ Acute Lymphoblastic Leukemia (ALL) Adult patients with relapsed or refractory Philadelphia chromosome positive acute lymphoblastic leukemia (Ph+ALL).
Imatinib OralIMKELDILabelled hereAdult Patients With Ph+ Acute Lymphoblastic Leukemia (ALL) Adult patients with relapsed or refractory Philadelphia chromosome positive acute lymphoblastic leukemia (Ph+ ALL).
Inotuzumab OzogamicinBesponsaLabelled hereBESPONSA is indicated for the treatment of relapsed or refractory CD22-positive B-cell precursor acute lymphoblastic leukemia (ALL) in adult and pediatric patients 1 year and older .
MercaptopurineMERCAPTOPURINE, Mercaptopurine, PURIXANLabelled hereAcute Lymphoblastic Leukemia PURIXAN is indicated for the treatment of patients with acute lymphoblastic leukemia (ALL) as part of a combination chemotherapy maintenance regimen.
NelarabineArranon, NELARABINE, NelarabineLabelled hereARRANON is indicated for the treatment of T-cell acute lymphoblastic leukemia (T-ALL) and T-cell lymphoblastic lymphoma (T-LBL) in adult and pediatric patients age 1 year and older whose disease has not responded to or has relapsed following treatment with at least 2 chemotherapy regimens.
Obecabtagene AutoleucelAUCATZYLLabelled here1 INDICATION AND USAGE AUCATZYL is indicated for the treatment of adults with relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL).
PegaspargaseONCASPARLabelled hereAcute lymphoblastic leukemia and hypersensitivity to asparaginase
PonatinibIclusigLabelled hereICLUSIG is a kinase inhibitor indicated for the treatment of adult patients with: Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia (Ph+ ALL) Newly diagnosed Ph+ ALL, in combination with chemotherapy.
SargramostimLeukineLabelled hereAutologous Peripheral Blood Progenitor Cell and Bone Marrow Transplantation LEUKINE is indicated for the acceleration of myeloid reconstitution following autologous peripheral blood progenitor cell (PBPC) or bone marrow transplantation in adult and pediatric patients 2 years of age and older with non-Hodgkin's lymphoma (NHL), acute lymphoblastic leukemia (ALL) and Hodgkin's lymphoma (HL).
TisagenlecleucelKYMRIAHLabelled herePediatric and Young Adult Relapsed or Refractory B-cell Acute Lymphoblastic Leukemia KYMRIAH is indicated for treatment of patients up to 25 years of age with B-cell precursor acute lymphoblastic leukemia (ALL) that is refractory or in second or later relapse.
CytarabineCYTARABINE, Cytarabine, cytarabineBackboneIt has also been found useful in the treatment of acute lymphocytic leukemia and the blast phase of chronic myelocytic leukemia.
DoxorubicinDOXOrubicin Hydrochloride, Doxorubicin Hydrochloride, Doxorubicin hydrochlorideBackbonefor the treatment of: acute lymphoblastic leukemia, acute myeloblastic leukemia, Hodgkin lymphoma, Non-Hodgkin lymphoma, metastatic breast cancer, metastatic Wilms' tumor, metastatic neuroblastoma, metastatic soft tissue sarcoma, metastatic bone sarcomas, metastatic ovarian carcinoma, metastatic transitional cell bladder carcinoma, metastatic thyroid carcinoma, metastatic gastric carcinoma, met...
MethotrexateJYLAMVO, METHOTREXATE, MethotrexateBackboneIn acute lymphocytic leukemia, methotrexate is indicated for use in maintenance therapy in combination with other chemotherapeutic agents.

55 labels match indications_and_usage:"acute lymphoblastic leukemia" OR indications_and_usage:"acute lymphocytic leukemia"; they collapse to 20 distinct molecules once salt forms, biosimilars and co-formulated hyaluronidase are merged. Source: openFDA drug label API (api.fda.gov/drug/label.json), retrieved 2026-09-12. Labels change; this reflects the current label text, not the approval history. Not prescribing guidance.

Cell therapy against CD19

ClinicalTrials.gov · retrieved 2026-09-12 · weekly

CD19 is the busiest cell-therapy antigen in acute lymphoblastic leukemia: 131 registered trials, 59 still active, 10 withdrawn before enrolling anyone.

TrialPhaseStatusTitleLast update
NCT04532281EARLY/1RecruitingA Study of Murine CD19 CAR-T Therapy for Patients With Relapsed or Refractory CD19+ B-cell Hematological Malignancies2020-10-26
NCT04603872EARLY/1RecruitingCAR-T Cells Combined With Dasatinib for Patients With Relapsed and/or Refractory B-cell Hematological Malignancies2020-10-28
NCT047462092RecruitingBlinatumomab After TCR Alpha Beta/CD19 Depleted HCT2021-09-17
NCT060814782RecruitingCD19/CD22 Bispecific CAR-T Cell Therapy for Relapsed/Refractory B-cell Lymphoma or Acute Lymphoblastic Leukemia2023-10-13
NCT06355739no phaseRecruitingCD19-targeted CAR T Cell Autotransfusion for the Treatment of Recurrent/Refractory B-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma in Children With CD19+2024-04-09
NCT061013811/2RecruitingCD19-directed CAR-T Cell Therapy for R/R Acute Leukemia and Lymphoma2024-12-09
NCT067354951/2RecruitingCD19 & CD22 Bispecific CAR T Cells in the Treatment of Relapsed/Refractory B Cell Hematologic Tumors2024-12-16
NCT067527851RecruitingCD19/CD22 CAR-T Cell Therapy in MRD-Positive B-lineage Acute Lymphoblastic Leukemia in Children.2024-12-31
NCT050542571RecruitingCART19 Cells Effects in Patients with Relapsed or Refractory Acute Lymphoblastic Leukemia and Non-Hodgkin's Lymphoma2025-01-06
NCT06866873no phaseRecruitingCD-19 CAR-T Cell for Pediatric ALL or Lymphoma2025-03-10

10 of 131 shown, most recently active first. Other antigens searched: CD22 (68), CD3 (38), CD7 (37), CD20 (27), CD38 (5), BCR-ABL1 (4). Source: ClinicalTrials.gov API v2, retrieved 2026-09-12. Trials are matched on the antigen named in the title or intervention, so a trial stating only a product code is missed.

Research momentum

PubMed MeSH · monthly

Every term below is a share of the acute lymphoblastic leukemia literature, not a count, because the field itself grew: 2015–2018 (n=4,192) against 2021–2025 (n=5,297). A topic whose papers doubled while the field doubled has not risen.

Rising, with a real baseline

MeSH term2015–182021–25ChangeShare now
Receptors, Chimeric Antigen0.67%6.08%9.1×322 papers
Bridged Bicyclo Compounds, Heterocyclic0.24%1.25%5.22×66 papers
Molecular Docking Simulation0.12%0.53%4.43×28 papers
Neural Networks, Computer0.12%0.45%3.8×24 papers
Immunotherapy, Adoptive2.15%7.72%3.6×409 papers
Hematologic Neoplasms0.21%0.72%3.34×38 papers
Antigens, CD70.12%0.4%3.32×21 papers
CRISPR-Cas Systems0.12%0.36%3.01×19 papers
Leukemia0.19%0.57%2.97×30 papers
Chronic Disease0.19%0.55%2.87×29 papers

Cooling

MeSH term2015–182021–25ChangeShare now
Gene Expression1.91%0.26%0.14×14 papers
Time Factors2.62%0.43%0.17×23 papers
Survival Analysis4.6%0.83%0.18×44 papers
Age Factors3.34%0.62%0.19×33 papers
Heterografts1.31%0.25%0.19×13 papers
Biopsy1.22%0.25%0.2×13 papers

Biggest topics now

MeSH term2015–182021–25ChangeShare now
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma13.93%16.35%1.17×866 papers
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma14.1%15.63%1.11×828 papers
Prognosis14.36%13.74%0.96×728 papers
Hematopoietic Stem Cell Transplantation9.18%11.33%1.23×600 papers
Antineoplastic Combined Chemotherapy Protocols14.07%10.08%0.72×534 papers
Recurrence9.06%9.61%1.06×509 papers
Treatment Outcome13.12%8.76%0.67×464 papers
Antineoplastic Agents13.24%8.29%0.63×439 papers
Neoplasm, Residual6.42%8.1%1.26×429 papers
Immunotherapy, Adoptive2.15%7.72%3.6×409 papers

Publication mix

Type2015–182021–25
Clinical Trial0.0%0.1%
Randomized Controlled Trial2.4%1.4%
Review11.0%9.6%
Meta-Analysis1.0%1.1%
Case Reports0.0%2.4%

Query: Precursor Cell Lymphoblastic Leukemia-Lymphoma[MeSH Major Topic] NOT ("Leukemia, Myeloid, Acute"[MeSH] OR "Leukemia, Myelogenous, Chronic, BCR-ABL Positive"[MeSH] OR "Lymphoma, Non-Hodgkin"[MeSH] OR "Leukemia, Lymphocytic, Chronic, B-Cell"[MeSH]). Terms need at least 12 papers in the recent window and, in the rising table, at least 5 in the earlier one — a term going from 1 paper to 12 is a large fold change and no evidence of anything. Ubiquitous descriptors (Humans, Animals, age bands) and the disease’s own term are dropped. Source: PubMed MeSH, retrieved 2026-09-12.

Disease burden

What the public sources count, and how closely each category matches this disease. The same figures for every disease on the site are on one table.

MeasureValueMatchWhat it counts
New cases each year6,250 cases/yeardirect2026
Deaths each year1,600 deaths/yeardirect2026
Incidence rate1.9 cases per 100,000 people per yeardirect2019-2023
Death rate0.4 deaths per 100,000 people per yeardirect2020-2024
People living with it126,118 people living with the diseasedirect2023
Median age at diagnosis18.0 yearsdirect2019-2023
median age at death60 yearsdirect2020-2024
Five-year relative survival73.2%direct2016-2022

Years of life lost

16.2 years per case, 101,170 a year, from survival and age at diagnosis rather than from a death count. derived proxy What this costs to fund is in Funding.

3 assumptions behind this estimate
  • Five-year relative survival stands in for cure; a death after five years is not counted.
  • The median age at diagnosis stands in for the whole age distribution.
  • Life expectancy at birth (78.4 years) is the reference, rather than remaining expectancy at the age of death from a life table.
  • Each assumption moves the result by more than the difference between the two diseases currently on this site, so this figure separates a disease from one ten times its size, not from a close neighbour.

Funding

NIH RePORTER · quarterly

NIH obligations naming acute lymphoblastic leukemia, after removing the 3,743 records across all years that matched the search but are about something else. That filter is not cosmetic: without it this section reports another field’s funding as this disease’s.

$33.2MNIH obligations, FY2025from $17.8M in FY2013 · +86%
67distinct projects funded51 in FY2013
$36.8Mpeak year was FY2018obligations, all institutes
96%of FY2025 awards from NCI69 of 72

NIH obligations by fiscal year

$9M$18M$28M$37M13151719212325
YearObligationsAwardsDistinct projectsDropped as off-topic
FY2013$17.8M5951242
FY2014$20.6M6963257
FY2015$25.7M7972249
FY2016$27.2M7969212
FY2017$29.0M7769257
FY2018$36.8M8276304
FY2019$30.7M8174276
FY2020$35.9M8381278
FY2021$30.6M8278315
FY2022$34.3M9383358
FY2023$34.0M7775351
FY2024$30.7M8274325
FY2025$33.2M7267319

Where FY2025 money went

InstitutionObligationsAwards
Seattle Children'S Hospital$3.5M0
St. Jude Children'S Research Hospital$2.9M6
Beckman Research Institute/City Of Hope$2.2M4
Thomas Jefferson University$1.7M3
New York University School Of Medicine$1.4M4
Division Of Basic Sciences - Nci$1.4M0
University Of Southern California$1.3M3
University Of Colorado Denver$1.2M3
Stanford University$1.0M2
University Of Michigan At Ann Arbor$1.0M3

Text search acute lymphoblastic leukemia over project title, terms and abstract, per fiscal year. Awards are individual funding actions; distinct projects collapse them by core project number, so a multi-year grant counts once. The most recent year may be incomplete. Source: NIH RePORTER, retrieved 2026-09-12.

What that buys

Against 101,170 years of life lost a year, FY2025 obligations are $328 per life-year — $5,314 per case. The estimate and its assumptions are in Disease burden.

Who funds it, FY2025

The total says how much. These say who from, through what kind of award, and to whom — which a dollar figure cannot.

NIH institutes

NCI69 · 96%
NIGMS1 · 1%
NHGRI1 · 1%
VA1 · 1%

Projects by administering institute. The rows above are the top 4 and account for 72 of 72.

Award mechanisms

R0138 · 53%
R376 · 8%
K084 · 6%
F303 · 4%
U543 · 4%
P013 · 4%

R01 is an investigator-initiated grant; ZIA is NIH intramural, meaning the work happens inside NIH rather than being funded outside it. The rows above are the top 15 and account for 69 of 72.

Where it lands

Seattle Children'S Hospital$3.5M · 10.5%
St. Jude Children'S Research Hospital$2.9M · 8.7%
Beckman Research Institute/City Of Hope$2.2M · 6.6%
Thomas Jefferson University$1.7M · 5.0%
New York University School Of Medicine$1.4M · 4.3%
Division Of Basic Sciences - Nci$1.4M · 4.2%

Share of $33.2M in FY2025. The top three hold 26%.

Public datasets, ranked

NCBI GEO + Europe PMC + iCite · weekly

2,016 human GEO series match acute lymphoblastic leukemia. Keyword relevance cannot tell a 1,099-sample patient cohort from a six-well cell-line experiment, so this ranking scores four things GEO does not expose: how often the accession is named in full-text papers, field-normalised citation impact, clinical annotation, and cohort type.

Composition of the 629-study ranked set

unspecified 199patient 176cell line 133mixed 106xenograft 15
199 unspecified176 patient133 cell line106 mixed15 xenograft319 carry clinical annotation185 carry survival32 patient cohorts ≥100 GEO samples39,025 GEO samples totalin 30 single-cell series a GEO sample is one cell, not one patient

Established

high reuse, older
AccessionStudySamplesMentionsEurope PMCRCREvidence
GSE33315Discovery of novel recurrent mutations and rearrangements in early T-cell precursor acute lymphoblastic leukaemia by whole genome sequencing2012 · array5752329.9
patient cohortAPT 0.95survivalmolecularETV6NOTCH11,338 cites
GSE12995Expression data for diagnosis acute lymphoblastic leukemia samples2008 · array1751422.3
mixedAPT 0.95survivalstagemolecularABL1BCR-ABL1IKZF11,132 cites
GSE11877Children's Oncology Group Study 9906 for High-Risk Pediatric ALL2009 · array207689.8
patient cohortAPT 0.95survivalstage447 cites
GSE49031Genome-wide signatures of differential DNA methylation in pediatric acute lymphoblastic leukemia2013 · methylation945317.7
patient cohortAPT 0.95survivalstage295 cites
GSE13425Expression data from ALL patients included in the set used to construct a classification signature (COALL cohort)2009 · array1902714.9
patient cohortAPT 0.95survivalmolecularBCR-ABL720 cites
GSE28497New markers for minimal residual disease detection in acute lymphoblastic leukemia2011 · array288206.2
patient cohortAPT 0.95molecularCD19248 cites
GSE26713Integrated transcript and genome analyses reveal NKX2-1 and MEF2C as potential oncogenes in T-ALL2011 · array124576.7
patient cohortAPT 0.75331 cites
GSE5511Genes regulating B cell development are mutated in acute lymphoid leukaemia2009 · array1,099126.1
patient cohortAPT 0.95molecularPAX51,440 cites

Recent

2022 onward, by score
AccessionStudySamplesMentionsEurope PMCRCREvidence
GSE181157Whole-transcriptome analysis in acute lymphoblastic leukemia: a report from the DFCI ALL Consortium Protocol 16-0012022 · sequencing17345.4
patient cohortAPT 0.75survivalmolecularETV6KMT2APAX573 cites
GSE227832Multimodal classification of molecular subtypes in pediatric acute lymphoblastic leukemia2023 · sequencing34052.0
mixedAPT 0.75survival22 cites
GSE235787Single-cell network pharmacology predicts total therapies targeting multiple developmental clones in B-cell acute lymphoblastic leukemia2024 · chromatin2043.5
mixedAPT 0.75survivalstage32 cites
GSE227122Pediatric T-cell acute lymphoblastic leukemia blast signature and MRD associated immune environment changes defined by single cell transcriptomics analysis.2023 · sequencing1681.4
patient cohortAPT 0.75survival6 cites
GSE263710Targeting signaling rewiring and resistant subpopulations in Philadelphia Chromosome-like Acute Lymphoblastic Leukemia [Bulk ATAC-seq]2025 · chromatin3913.4
mixedAPT 0.75survivalstage13 cites
GSE195964Combination therapy with nilotinib and PDL1 blockade reverses CD4 T cell dysfunction and prevents relapse in acute B cell leukemia2022 · single-cell612.6
patient cohortAPT 0.75survivalmolecularBCR-ABLBISPECIFIC48 cites

Sources: NCBI GEO + Europe PMC + iCite, retrieved 2026-09-12. SubSeries are collapsed to one row per study by linked PMID. Of 2,016 series retrieved, 203 were dropped by the profile’s exclusion rules and 845 named the disease only in passing. The ranked set is a relevance-ranked sample, not a census, so the composition figures describe the sample only.

Where the gaps are

Derived from the sections above · recomputed on every refresh

Each card below is a disagreement between two of the tables on this page — a drug that exists but was never tried here, a target that looks tested and was not, a gene with no drug whose product has a busy clinical programme. They are computed from the same facts as the tables, so they cannot contradict them.

IKZF1

No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.

CDKN2A

No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.

ETV6

No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.

PAX5

No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.

CRLF2

No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.

How a machine reads this page

Static

This page is written to be quoted correctly by a model as much as read by a person. The same facts are available as JSON at the sibling URL below, which is what to cite. The cross-disease layer — burden, genes, drugs and antigens across every briefing — is described at /disease/api.json.

Fully server-rendered

Every figure is in the HTML at first byte. No JavaScript runs, no figure is fetched after load, and nothing on this page requires a renderer to see.

Every number carries a source

Each section names the API it came from and the date it was retrieved: Open Targets (2026-09-12), ClinicalTrials.gov (2026-09-12), openFDA (2026-09-12), NCBI GEO (2026-09-12), PubMed (2026-09-12), NIH RePORTER (2026-09-12).

Negatives stated explicitly

Where nothing exists for acute lymphoblastic leukemia — no drug, no trial, no approval — the page says so in those words rather than omitting the row. An absent row is unquotable; a stated negative is the finding.

Denominators, not just percentages

Every share is printed with the count and the total it came from, so a figure can be checked rather than taken.

The filters are published

5 exclusion patterns are applied to free text before anything is ranked, because Jurkat is used as a model system in T-cell activation, TCR signalling and reporter assays; the immunology default T-cell line. What was removed and why is stated in each section rather than silently applied.

{
  "disease": "Acute lymphoblastic leukemia",
  "mesh": "Precursor Cell Lymphoblastic Leukemia-Lymphoma",
  "facts": "https://usebiotransfer.org/disease/acute-lymphoblastic-leukemia.json",
  "methods": "https://usebiotransfer.org/methods/",
  "all_diseases": "https://usebiotransfer.org/disease/api.json",
  "note": "Every figure on the page is in that JSON with its source and retrieval date. Quote from it rather than from the HTML."
}