Target landscape
Open Targets · retrieved 2026-09-12 · weekly12 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.
| Gene | Drugs | Approval, and whether it reached this disease | Open Targets tractabilitycomputed from protein features and literature — a signal that a modality is worth trying, not evidence that it works | Cell 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 · weekly17 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.
Every label that names acute lymphoblastic leukemia
| Drug | Role | What the label says |
|---|---|---|
| Asparaginase Erwinia Chrysanthemi (Recombinant)-RywnRylaze | Labelled here | RYLAZE 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. |
| BlinatumomabBLINCYTO | Labelled here | Relapsed or refractory CD19-positive B-cell precursor acute lymphoblastic leukemia (ALL). |
| Brexucabtagene AutoleucelTECARTUS | Labelled here | Acute Lymphoblastic Leukemia TECARTUS is indicated for the treatment of adult patients with relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL). |
| Calaspargase Pegolasparlas | Labelled here | Acute 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, Clofarabine | Labelled here | Clofarabine 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, PHYRAGO | Labelled here | Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) with resistance or intolerance to prior therapy. |
| DaunorubicinDaunorubicin Hydrochloride, daunorubicin hydrochloride | Labelled here | Daunorubicin 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, Imatinib | Labelled here | Adult Patients With Ph+ Acute Lymphoblastic Leukemia (ALL) Adult patients with relapsed or refractory Philadelphia chromosome positive acute lymphoblastic leukemia (Ph+ALL). |
| Imatinib OralIMKELDI | Labelled here | Adult Patients With Ph+ Acute Lymphoblastic Leukemia (ALL) Adult patients with relapsed or refractory Philadelphia chromosome positive acute lymphoblastic leukemia (Ph+ ALL). |
| Inotuzumab OzogamicinBesponsa | Labelled here | BESPONSA 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, PURIXAN | Labelled here | Acute 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, Nelarabine | Labelled here | ARRANON 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 AutoleucelAUCATZYL | Labelled here | 1 INDICATION AND USAGE AUCATZYL is indicated for the treatment of adults with relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL). |
| PegaspargaseONCASPAR | Labelled here | Acute lymphoblastic leukemia and hypersensitivity to asparaginase |
| PonatinibIclusig | Labelled here | ICLUSIG 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. |
| SargramostimLeukine | Labelled here | Autologous 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). |
| TisagenlecleucelKYMRIAH | Labelled here | Pediatric 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, cytarabine | Backbone | It 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 hydrochloride | Backbone | for 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, Methotrexate | Backbone | In 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 · weeklyCD19 is the busiest cell-therapy antigen in acute lymphoblastic leukemia: 131 registered trials, 59 still active, 10 withdrawn before enrolling anyone.
| Trial | Phase | Status | Title | Last update |
|---|---|---|---|---|
| NCT04532281 | EARLY/1 | Recruiting | A Study of Murine CD19 CAR-T Therapy for Patients With Relapsed or Refractory CD19+ B-cell Hematological Malignancies | 2020-10-26 |
| NCT04603872 | EARLY/1 | Recruiting | CAR-T Cells Combined With Dasatinib for Patients With Relapsed and/or Refractory B-cell Hematological Malignancies | 2020-10-28 |
| NCT04746209 | 2 | Recruiting | Blinatumomab After TCR Alpha Beta/CD19 Depleted HCT | 2021-09-17 |
| NCT06081478 | 2 | Recruiting | CD19/CD22 Bispecific CAR-T Cell Therapy for Relapsed/Refractory B-cell Lymphoma or Acute Lymphoblastic Leukemia | 2023-10-13 |
| NCT06355739 | no phase | Recruiting | CD19-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 |
| NCT06101381 | 1/2 | Recruiting | CD19-directed CAR-T Cell Therapy for R/R Acute Leukemia and Lymphoma | 2024-12-09 |
| NCT06735495 | 1/2 | Recruiting | CD19 & CD22 Bispecific CAR T Cells in the Treatment of Relapsed/Refractory B Cell Hematologic Tumors | 2024-12-16 |
| NCT06752785 | 1 | Recruiting | CD19/CD22 CAR-T Cell Therapy in MRD-Positive B-lineage Acute Lymphoblastic Leukemia in Children. | 2024-12-31 |
| NCT05054257 | 1 | Recruiting | CART19 Cells Effects in Patients with Relapsed or Refractory Acute Lymphoblastic Leukemia and Non-Hodgkin's Lymphoma | 2025-01-06 |
| NCT06866873 | no phase | Recruiting | CD-19 CAR-T Cell for Pediatric ALL or Lymphoma | 2025-03-10 |
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 · monthlyEvery 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 term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Receptors, Chimeric Antigen | 0.67% | 6.08% | 9.1× | 322 papers |
| Bridged Bicyclo Compounds, Heterocyclic | 0.24% | 1.25% | 5.22× | 66 papers |
| Molecular Docking Simulation | 0.12% | 0.53% | 4.43× | 28 papers |
| Neural Networks, Computer | 0.12% | 0.45% | 3.8× | 24 papers |
| Immunotherapy, Adoptive | 2.15% | 7.72% | 3.6× | 409 papers |
| Hematologic Neoplasms | 0.21% | 0.72% | 3.34× | 38 papers |
| Antigens, CD7 | 0.12% | 0.4% | 3.32× | 21 papers |
| CRISPR-Cas Systems | 0.12% | 0.36% | 3.01× | 19 papers |
| Leukemia | 0.19% | 0.57% | 2.97× | 30 papers |
| Chronic Disease | 0.19% | 0.55% | 2.87× | 29 papers |
Cooling
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Gene Expression | 1.91% | 0.26% | 0.14× | 14 papers |
| Time Factors | 2.62% | 0.43% | 0.17× | 23 papers |
| Survival Analysis | 4.6% | 0.83% | 0.18× | 44 papers |
| Age Factors | 3.34% | 0.62% | 0.19× | 33 papers |
| Heterografts | 1.31% | 0.25% | 0.19× | 13 papers |
| Biopsy | 1.22% | 0.25% | 0.2× | 13 papers |
Biggest topics now
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Precursor T-Cell Lymphoblastic Leukemia-Lymphoma | 13.93% | 16.35% | 1.17× | 866 papers |
| Precursor B-Cell Lymphoblastic Leukemia-Lymphoma | 14.1% | 15.63% | 1.11× | 828 papers |
| Prognosis | 14.36% | 13.74% | 0.96× | 728 papers |
| Hematopoietic Stem Cell Transplantation | 9.18% | 11.33% | 1.23× | 600 papers |
| Antineoplastic Combined Chemotherapy Protocols | 14.07% | 10.08% | 0.72× | 534 papers |
| Recurrence | 9.06% | 9.61% | 1.06× | 509 papers |
| Treatment Outcome | 13.12% | 8.76% | 0.67× | 464 papers |
| Antineoplastic Agents | 13.24% | 8.29% | 0.63× | 439 papers |
| Neoplasm, Residual | 6.42% | 8.1% | 1.26× | 429 papers |
| Immunotherapy, Adoptive | 2.15% | 7.72% | 3.6× | 409 papers |
Publication mix
| Type | 2015–18 | 2021–25 |
|---|---|---|
| Clinical Trial | 0.0% | 0.1% |
| Randomized Controlled Trial | 2.4% | 1.4% |
| Review | 11.0% | 9.6% |
| Meta-Analysis | 1.0% | 1.1% |
| Case Reports | 0.0% | 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.
| Measure | Value | Match | What it counts |
|---|---|---|---|
| New cases each year | 6,250 cases/year | direct | 2026 SEER Cancer Stat Facts, Leukemia - Acute Lymphocytic Leukemia (ALL), retrieved 2026-09-12 |
| Deaths each year | 1,600 deaths/year | direct | 2026 SEER Cancer Stat Facts, Leukemia - Acute Lymphocytic Leukemia (ALL), retrieved 2026-09-12 |
| Incidence rate | 1.9 cases per 100,000 people per year | direct | 2019-2023 SEER Cancer Stat Facts, Leukemia - Acute Lymphocytic Leukemia (ALL), retrieved 2026-09-12 |
| Death rate | 0.4 deaths per 100,000 people per year | direct | 2020-2024 SEER Cancer Stat Facts, Leukemia - Acute Lymphocytic Leukemia (ALL), retrieved 2026-09-12 |
| People living with it | 126,118 people living with the disease | direct | 2023 SEER Cancer Stat Facts, Leukemia - Acute Lymphocytic Leukemia (ALL), retrieved 2026-09-12 |
| Median age at diagnosis | 18.0 years | direct | 2019-2023 SEER Cancer Stat Facts, Leukemia - Acute Lymphocytic Leukemia (ALL), retrieved 2026-09-12 |
| median age at death | 60 years | direct | 2020-2024 SEER Cancer Stat Facts, Leukemia - Acute Lymphocytic Leukemia (ALL), retrieved 2026-09-12 |
| Five-year relative survival | 73.2% | direct | 2016-2022 SEER Cancer Stat Facts, Leukemia - Acute Lymphocytic Leukemia (ALL), retrieved 2026-09-12 |
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 · quarterlyNIH 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.
NIH obligations by fiscal year
| Year | Obligations | Awards | Distinct projects | Dropped as off-topic |
|---|---|---|---|---|
| FY2013 | $17.8M | 59 | 51 | 242 |
| FY2014 | $20.6M | 69 | 63 | 257 |
| FY2015 | $25.7M | 79 | 72 | 249 |
| FY2016 | $27.2M | 79 | 69 | 212 |
| FY2017 | $29.0M | 77 | 69 | 257 |
| FY2018 | $36.8M | 82 | 76 | 304 |
| FY2019 | $30.7M | 81 | 74 | 276 |
| FY2020 | $35.9M | 83 | 81 | 278 |
| FY2021 | $30.6M | 82 | 78 | 315 |
| FY2022 | $34.3M | 93 | 83 | 358 |
| FY2023 | $34.0M | 77 | 75 | 351 |
| FY2024 | $30.7M | 82 | 74 | 325 |
| FY2025 | $33.2M | 72 | 67 | 319 |
Where FY2025 money went
| Institution | Obligations | Awards |
|---|---|---|
| Seattle Children'S Hospital | $3.5M | 0 |
| St. Jude Children'S Research Hospital | $2.9M | 6 |
| Beckman Research Institute/City Of Hope | $2.2M | 4 |
| Thomas Jefferson University | $1.7M | 3 |
| New York University School Of Medicine | $1.4M | 4 |
| Division Of Basic Sciences - Nci | $1.4M | 0 |
| University Of Southern California | $1.3M | 3 |
| University Of Colorado Denver | $1.2M | 3 |
| Stanford University | $1.0M | 2 |
| University Of Michigan At Ann Arbor | $1.0M | 3 |
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
Projects by administering institute. The rows above are the top 4 and account for 72 of 72.
Award mechanisms
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
Share of $33.2M in FY2025. The top three hold 26%.
Public datasets, ranked
NCBI GEO + Europe PMC + iCite · weekly2,016 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
Established
high reuse, older| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE33315 | Discovery of novel recurrent mutations and rearrangements in early T-cell precursor acute lymphoblastic leukaemia by whole genome sequencing2012 · array | 575 | 23 | 29.9 | patient cohortAPT 0.95survivalmolecularETV6NOTCH11,338 cites |
| GSE12995 | Expression data for diagnosis acute lymphoblastic leukemia samples2008 · array | 175 | 14 | 22.3 | mixedAPT 0.95survivalstagemolecularABL1BCR-ABL1IKZF11,132 cites |
| GSE11877 | Children's Oncology Group Study 9906 for High-Risk Pediatric ALL2009 · array | 207 | 68 | 9.8 | patient cohortAPT 0.95survivalstage447 cites |
| GSE49031 | Genome-wide signatures of differential DNA methylation in pediatric acute lymphoblastic leukemia2013 · methylation | 945 | 31 | 7.7 | patient cohortAPT 0.95survivalstage295 cites |
| GSE13425 | Expression data from ALL patients included in the set used to construct a classification signature (COALL cohort)2009 · array | 190 | 27 | 14.9 | patient cohortAPT 0.95survivalmolecularBCR-ABL720 cites |
| GSE28497 | New markers for minimal residual disease detection in acute lymphoblastic leukemia2011 · array | 288 | 20 | 6.2 | patient cohortAPT 0.95molecularCD19248 cites |
| GSE26713 | Integrated transcript and genome analyses reveal NKX2-1 and MEF2C as potential oncogenes in T-ALL2011 · array | 124 | 57 | 6.7 | patient cohortAPT 0.75331 cites |
| GSE5511 | Genes regulating B cell development are mutated in acute lymphoid leukaemia2009 · array | 1,099 | 1 | 26.1 | patient cohortAPT 0.95molecularPAX51,440 cites |
Recent
2022 onward, by score| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE181157 | Whole-transcriptome analysis in acute lymphoblastic leukemia: a report from the DFCI ALL Consortium Protocol 16-0012022 · sequencing | 173 | 4 | 5.4 | patient cohortAPT 0.75survivalmolecularETV6KMT2APAX573 cites |
| GSE227832 | Multimodal classification of molecular subtypes in pediatric acute lymphoblastic leukemia2023 · sequencing | 340 | 5 | 2.0 | mixedAPT 0.75survival22 cites |
| GSE235787 | Single-cell network pharmacology predicts total therapies targeting multiple developmental clones in B-cell acute lymphoblastic leukemia2024 · chromatin | 20 | 4 | 3.5 | mixedAPT 0.75survivalstage32 cites |
| GSE227122 | Pediatric T-cell acute lymphoblastic leukemia blast signature and MRD associated immune environment changes defined by single cell transcriptomics analysis.2023 · sequencing | 16 | 8 | 1.4 | patient cohortAPT 0.75survival6 cites |
| GSE263710 | Targeting signaling rewiring and resistant subpopulations in Philadelphia Chromosome-like Acute Lymphoblastic Leukemia [Bulk ATAC-seq]2025 · chromatin | 39 | 1 | 3.4 | mixedAPT 0.75survivalstage13 cites |
| GSE195964 | Combination therapy with nilotinib and PDL1 blockade reverses CD4 T cell dysfunction and prevents relapse in acute B cell leukemia2022 · single-cell | 6 | 1 | 2.6 | 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 refreshEach 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
StaticThis 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."
}