Target landscape
Open Targets · retrieved 2026-09-11 · weekly13 genes recurrently implicated in acute myeloid leukemia, triaged for whether anything can actually be aimed at them. The zeros are the informative rows.
Of 13 recurrently implicated genes, 12 carry any drug at all. That is a statement about these 13 gene targets, not about the disease: Acute myeloid leukemia does have labelled therapy — 17 drugs, listed in the next section.
Two different questions
The table below asks what can be aimed at 13 recurrently implicated genes. That is narrower than what is approved for the disease, and narrower again than what acute myeloid 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 |
|---|---|---|---|---|
| FLT3 | 39 | 10 approvedFedratinib, Gilteritinib, Lestaurtinib, Midostaurin, Pacritinib, Pexidartinib, Quizartinib, Sorafenib, Sunitinib, Sunitinib MalateApproved in acute myeloid leukemia: Gilteritinib, Quizartinib.80 active of 249 acute myeloid leukemia trials | antibody, other clinical modality, protein degrader, small molecule | 4 active of 5 trials |
| NPM1 | 2 | 2 approvedCeritinib, CrizotinibApproved in non-small cell lung carcinoma. No acute myeloid leukemia indication appears on these drugs’ labels.2 trials, none active | protein degrader, small molecule | — |
| IDH1 | 7 | 3 approvedIvosidenib, Olutasidenib, VorasidenibApproved in acute myeloid leukemia: Ivosidenib, Olutasidenib.45 active of 53 acute myeloid leukemia trials | antibody, protein degrader, small molecule | — |
| IDH2 | 2 | 2 approvedEnasidenib, VorasidenibApproved in acute myeloid leukemia: Enasidenib.19 active of 32 acute myeloid leukemia trials | protein degrader, small molecule | — |
| KMT2A | 2 | Phase 3Revumenib, Revumenib Sesquifumarate15 active of 17 acute myeloid leukemia trials | protein degrader, small molecule | — |
| MEN1 | 2 | 1 approvedRevumenibApproved in acute myeloid leukemia: Revumenib.15 active of 17 acute myeloid leukemia trials | protein degrader, small molecule | — |
| DNMT3A | 2 | 2 approvedAzacitidine, DecitabineApproved in acute myeloid leukemia: Azacitidine.138 active of 388 acute myeloid leukemia trials | protein degrader, small molecule | — |
| TP53 | 8 | Phase 3Alrizomadlin, Cenersen, Contusugene Ladenovec, Eprenetapopt, Idasanutlin, Navtemadlin, Siremadlin, Teprasiran2 active of 18 acute myeloid leukemia trials | other clinical modality, protein degrader, small molecule | — |
| BCL2 | 5 | 3 approvedNavitoclax, Oblimersen, VenetoclaxApproved in acute myeloid leukemia: Venetoclax.120 active of 201 acute myeloid leukemia trials | antibody, other clinical modality, protein degrader, small molecule | — |
| CD33 | 5 | 1 approvedGemtuzumab OzogamicinApproved in acute myeloid leukemia: Gemtuzumab Ozogamicin.46 active of 225 acute myeloid leukemia trials | antibody, other clinical modality, protein degrader, small molecule | 16 active of 36 trials |
| IL3RA | 5 | 1 approvedTagraxofuspApproved in acute myeloid leukemia by FAB classification, CD4+/CD56+ hematodermic neoplasm, lymphoma. No acute myeloid leukemia indication appears on these drugs’ labels.12 active of 24 acute myeloid leukemia trials | antibody, other clinical modality, protein degrader, small molecule | 12 active of 29 trials |
| KIT | 33 | 15 approvedAvapritinib, Cediranib, Dasatinib, Imatinib, Masitinib, Midostaurin, Pazopanib, Pexidartinib, Quizartinib, Regorafenib, Ripretinib, Sorafenib, Sunitinib, Sunitinib Malate, TivozanibApproved in acute myeloid leukemia: Quizartinib.54 active of 276 acute myeloid leukemia trials | antibody, protein degrader, small molecule | — |
| CEBPA | 0 | No drug— | protein degrader | — |
Dataset evidence counts studies in the 397-study ranked set whose title or abstract names the gene; the bar is scaled to FLT3. Sources: Open Targets Platform and NCBI GEO, retrieved 2026-09-11. 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 myeloid leukemia: (Daunorubicin And Cytarabine), Azacitidine, Cedazuridine And Decitabine, Enasidenib, Gemtuzumab Ozogamicin, Gilteritinib, Glasdegib, Idarubicin, Ivosidenib, Olutasidenib, Quizartinib, Revumenib, Rydapt, Sargramostim, Treosulfan, Venetoclax, Ziftomenib. Separately, 24 of the drugs returned for the genes in the table above are approved only for other diseases and reach acute myeloid leukemia through trials, not through their labels.
Every label that names acute myeloid leukemia
| Drug | Role | What the label says |
|---|---|---|
| (Daunorubicin And Cytarabine)VYXEOS | Labelled here | VYXEOS is indicated for the treatment of newly diagnosed therapy-related acute myeloid leukemia (t-AML) or AML with myelodysplasia-related changes (AML-MRC) in adults and pediatric patients 1 year and older. |
| AzacitidineONUREG | Labelled here | ONUREG is indicated for continued treatment of adult patients with acute myeloid leukemia who achieved first complete remission (CR) or complete remission with incomplete blood count recovery (CRi) following intensive induction chemotherapy and are not able to complete intensive curative therapy. |
| Cedazuridine And DecitabineINQOVI | Labelled here | Acute Myeloid Leukemia INQOVI is indicated in combination with venetoclax for the treatment of newly diagnosed acute myeloid leukemia (AML) in adults 75 years or older, or who have comorbidities that preclude use of intensive induction chemotherapy. |
| EnasidenibIdhifa | Labelled here | Acute Myeloid Leukemia IDHIFA is indicated for the treatment of adult patients with relapsed or refractory acute myeloid leukemia (AML) with an isocitrate dehydrogenase-2 (IDH2) mutation as detected by an FDA-approved test. |
| Gemtuzumab OzogamicinMylotarg | Labelled here | Newly-Diagnosed CD33-positive Acute Myeloid Leukemia (AML) MYLOTARG is indicated for the treatment of newly-diagnosed CD33-positive acute myeloid leukemia in adults and pediatric patients 1 month and older. |
| GilteritinibXospata | Labelled here | Relapsed or Refractory Acute Myeloid Leukemia XOSPATA is indicated for the treatment of adult patients who have relapsed or refractory acute myeloid leukemia (AML) with a FMS-like tyrosine kinase 3 (FLT3) mutation as detected by an FDA-approved test. |
| GlasdegibDaurismo | Labelled here | DAURISMO is indicated, in combination with low-dose cytarabine, for the treatment of newly-diagnosed acute myeloid leukemia (AML) in adult patients who are ≥75 years old or who have comorbidities that preclude use of intensive induction chemotherapy. |
| IdarubicinIdamycin PFS, Idarubicin Hydrochloride | Labelled here | IDAMYCIN PFS is indicated for the treatment of adult patients with acute myeloid leukemia (AML) as a component of a combination chemotherapy regimen. |
| IvosidenibTIBSOVO | Labelled here | Newly Diagnosed Acute Myeloid Leukemia TIBSOVO is indicated in combination with azacitidine or as monotherapy for the treatment of newly diagnosed acute myeloid leukemia (AML) with a susceptible isocitrate dehydrogenase-1 (IDH1) mutation as detected by an FDA-approved test in adults 75 years or older, or who have comorbidities that preclude use of intensive induction chemotherapy [see Dosage an... |
| OlutasidenibREZLIDHIA | Labelled here | Relapsed or Refractory Acute Myeloid Leukemia REZLIDHIA is indicated for the treatment of adult patients with relapsed or refractory acute myeloid leukemia (AML) with a susceptible isocitrate dehydrogenase-1 (IDH1) mutation as detected by an FDA-approved test [see Dosage and Administration |
| QuizartinibVANFLYTA | Labelled here | VANFLYTA is a kinase inhibitor indicated in combination with standard cytarabine and anthracycline induction and cytarabine consolidation, and as maintenance monotherapy following consolidation chemotherapy, for the treatment of adult patients with newly diagnosed acute myeloid leukemia (AML) that is FLT3 internal tandem duplication (ITD)-positive as detected by an FDA-approved test. |
| RevumenibRevuforj | Labelled here | ( 1 ) the treatment of relapsed or refractory acute myeloid leukemia (AML) with a susceptible nucleophosmin 1 ( NPM1 ) mutation in adult and pediatric patients 1 year and older who have no satisfactory alternative treatment options. |
| RydaptRYDAPT | Labelled here | Acute Myeloid Leukemia RYDAPT is indicated in combination with standard cytarabine and daunorubicin induction and cytarabine consolidation chemotherapy, for the treatment of adult patients with newly diagnosed acute myeloid leukemia (AML) who are FLT3 mutation-positive, as detected by an FDA approved test [see Dosage and Administration |
| SargramostimLeukine | Labelled here | Acute Myeloid Leukemia Following Induction Chemotherapy LEUKINE is indicated to shorten time to neutrophil recovery and to reduce the incidence of severe, life-threatening, or fatal infections following induction chemotherapy in adult patients 55 years and older with acute myeloid leukemia (AML). |
| TreosulfanGRAFAPEX | Labelled here | Acute Myeloid Leukemia GRAFAPEX is indicated in combination with fludarabine as a preparative regimen for allogeneic hematopoietic stem cell transplantation in adult and pediatric patients 1 year of age and older with acute myeloid leukemia (AML). |
| VenetoclaxVenclexta | Labelled here | Acute Myeloid Leukemia VENCLEXTA is indicated in combination with azacitidine, or decitabine, or low-dose cytarabine for the treatment of newly diagnosed acute myeloid leukemia (AML) in adults 75 years or older, or who have comorbidities that preclude use of intensive induction chemotherapy. |
| ZiftomenibKomzifti | Labelled here | KOMZIFTI is a menin inhibitor indicated for the treatment of adult patients with relapsed or refractory acute myeloid leukemia (AML) with a susceptible nucleophosmin 1 ( NPM1 ) mutation who have no satisfactory alternative treatment options. |
| FilgrastimFILKRI, NEUPOGEN, NYPOZI | Backbone | Patients with Acute Myeloid Leukemia Receiving Induction or Consolidation Chemotherapy NYPOZI is indicated for reducing the time to neutrophil recovery and the duration of fever, following induction or consolidation chemotherapy treatment of patients with acute myeloid leukemia (AML) [see Clinical Studies |
38 labels match indications_and_usage:"acute myeloid leukemia"; they collapse to 18 distinct molecules once salt forms, biosimilars and co-formulated hyaluronidase are merged. Source: openFDA drug label API (api.fda.gov/drug/label.json), retrieved 2026-09-11. Labels change; this reflects the current label text, not the approval history. Not prescribing guidance.
Cell therapy against CD33
ClinicalTrials.gov · retrieved 2026-09-11 · weeklyCD33 is the busiest cell-therapy antigen in acute myeloid leukemia: 36 registered trials, 16 still active, 2 withdrawn before enrolling anyone.
| Trial | Phase | Status | Title | Last update |
|---|---|---|---|---|
| NCT06420063 | 1/2 | Recruiting | Sequential CAR-T Cells Targeting CD33/CD123 in Patients With Acute Myelocytic Leukemia AML | 2024-11-12 |
| NCT06762132 | EARLY/1 | Recruiting | A Clinical Study to Explore the Safety and Efficacy of CD33 CAR-T Cell in Relapsed/Refractory Acute Myeloid Leukemia | 2025-01-07 |
| NCT05105152 | 1 | Recruiting | PLAT-08: A Study Of SC-DARIC33 CAR T Cells In Pediatric And Young Adults With Relapsed Or Refractory CD33+ AML | 2025-12-23 |
| NCT05672147 | 1 | Recruiting | CD33-CAR T Cell Therapy for the Treatment of Recurrent or Refractory Acute Myeloid Leukemia | 2026-03-05 |
| NCT07523555 | 1/2 | Recruiting | Adaptive Dual-Target CAR-T Cells for Relapsed or Refractory Hematologic Malignancies | 2026-04-13 |
| NCT06326021 | 1 | Recruiting | Optimised CD33 (FL-33) CAR T Therapy for Refractory/Relapsed Acute Myeloid Leukaemia | 2026-05-22 |
| NCT07668557 | 1 | Recruiting | Anti-CD33-CLL1 CAR-T Cells (ICG415) for the Treatment of Relapsed/Refractory Acute Myeloid Leukemia | 2026-06-25 |
| NCT05945849 | 1 | Recruiting | CD33KO-HSPC Infusion Followed by CART-33 Infusion(s) for Refractory/Relapsed AML | 2026-07-09 |
| NCT03927261 | 1 | Active | PRGN-3006 Adoptive Cellular Therapy for CD33-Positive Relapsed or Refractory AML, MRD Positive AML or Higher Risk MDS | 2024-11-08 |
| NCT03971799 | 1/2 | Active | Study of Anti-CD33 Chimeric Antigen Receptor-Expressing T Cells (CD33CART) in Children and Young Adults With Relapsed/Refractory Acute Myeloid Leukemia | 2025-07-14 |
10 of 36 shown, most recently active first. Other antigens searched: CD123 (29), CLL-1 (29), WT1 (15), CD7 (11), CD70 (6), NKG2D (6), FLT3 (5). Source: ClinicalTrials.gov API v2, retrieved 2026-09-11. 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 myeloid leukemia literature, not a count, because the field itself grew: 2015–2018 (n=6,000) against 2021–2025 (n=6,000). A topic whose papers doubled while the field doubled has not risen.
These are sample shares. The two windows hold 7,075 and 11,551 papers; MeSH terms were read from an evenly spaced sample of 6,000 and 6,000 of them, taken across the whole window rather than from its most recent papers. Percentages carry sampling error of roughly a percentage point and small differences between two terms are not meaningful.
Rising, with a real baseline
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Receptors, Chimeric Antigen | 0.08% | 1.52% | 18.18× | 91 papers |
| Bridged Bicyclo Compounds, Heterocyclic | 0.62% | 7.65% | 12.4× | 459 papers |
| Sulfonamides | 1.03% | 7.82% | 7.56× | 469 papers |
| RNA, Circular | 0.08% | 0.62% | 7.39× | 37 papers |
| Aniline Compounds | 0.25% | 1.18% | 4.73× | 71 papers |
| Pyrazines | 0.25% | 1.12% | 4.47× | 67 papers |
| Inflammation | 0.15% | 0.58% | 3.89× | 35 papers |
| Tumor Microenvironment | 1.02% | 3.78% | 3.72× | 227 papers |
| Molecular Docking Simulation | 0.23% | 0.8% | 3.43× | 48 papers |
| Myeloproliferative Disorders | 0.63% | 2.03% | 3.21× | 122 papers |
Cooling
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Survival Analysis | 6.57% | 0.65% | 0.1× | 39 papers |
| Real-Time Polymerase Chain Reaction | 2.0% | 0.2% | 0.1× | 12 papers |
| Biopsy | 1.62% | 0.22% | 0.13× | 13 papers |
| Gene Expression | 2.63% | 0.33% | 0.13× | 20 papers |
| Kaplan-Meier Estimate | 3.87% | 0.53% | 0.14× | 32 papers |
| Tumor Cells, Cultured | 3.45% | 0.47% | 0.14× | 28 papers |
Biggest topics now
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Mutation | 15.68% | 17.37% | 1.11× | 1042 papers |
| Prognosis | 18.27% | 17.17% | 0.94× | 1030 papers |
| Hematopoietic Stem Cell Transplantation | 12.4% | 13.88% | 1.12× | 833 papers |
| Antineoplastic Combined Chemotherapy Protocols | 13.68% | 11.58% | 0.85× | 695 papers |
| Apoptosis | 8.67% | 8.33% | 0.96× | 500 papers |
| Myelodysplastic Syndromes | 8.73% | 8.25% | 0.94× | 495 papers |
| Antineoplastic Agents | 12.97% | 8.0% | 0.62× | 480 papers |
| Sulfonamides | 1.03% | 7.82% | 7.56× | 469 papers |
| Bridged Bicyclo Compounds, Heterocyclic | 0.62% | 7.65% | 12.4× | 459 papers |
| Treatment Outcome | 14.07% | 7.48% | 0.53× | 449 papers |
Publication mix
| Type | 2015–18 | 2021–25 |
|---|---|---|
| Clinical Trial | 0.1% | 0.1% |
| Randomized Controlled Trial | 1.9% | 1.2% |
| Review | 11.8% | 10.1% |
| Meta-Analysis | 0.7% | 0.7% |
| Case Reports | 0.0% | 1.9% |
Query: Leukemia, Myeloid, Acute[MeSH Major Topic] NOT ("Leukemia, Myelogenous, Chronic, BCR-ABL Positive"[MeSH] OR "Precursor Cell Lymphoblastic Leukemia-Lymphoma"[MeSH] OR "Leukemia, Myelomonocytic, Chronic"[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. Windows are read whole where they fit and sampled where they do not; the totals and the sample sizes are both in the JSON beside this page. Source: PubMed MeSH, retrieved 2026-09-11.
Disease burden
What the public sources count, and how closely each category matches this disease.
| Measure | Value | Match | What it counts |
|---|---|---|---|
| New cases each year | 22,720 cases/year | direct | 2026 SEER Cancer Stat Facts, Acute Myeloid Leukemia, retrieved 2026-09-11 |
| Deaths each year | 11,500 deaths/year | direct | 2026 SEER Cancer Stat Facts, Acute Myeloid Leukemia, retrieved 2026-09-11 |
| Incidence rate | 4.4 cases per 100,000 per year | direct | 2019-2023 SEER Cancer Stat Facts, Acute Myeloid Leukemia, retrieved 2026-09-11 |
| Death rate | 2.7 deaths per 100,000 per year | direct | 2020-2024 SEER Cancer Stat Facts, Acute Myeloid Leukemia, retrieved 2026-09-11 |
| People living with it | 83,311 people living with the disease | direct | 2023 SEER Cancer Stat Facts, Acute Myeloid Leukemia, retrieved 2026-09-11 |
| Median age at diagnosis | 70.0 years | direct | 2019-2023 SEER Cancer Stat Facts, Acute Myeloid Leukemia, retrieved 2026-09-11 |
| median age at death | 74 years | direct | 2020-2024 SEER Cancer Stat Facts, Acute Myeloid Leukemia, retrieved 2026-09-11 |
| Five-year relative survival | 33.4% | direct | 2016-2022 SEER Cancer Stat Facts, Acute Myeloid Leukemia, retrieved 2026-09-11 |
Years of life lost
5.6 years per case, 127,105 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 myeloid leukemia, after removing the 4,785 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 | $59.6M | 161 | 139 | 346 |
| FY2014 | $69.1M | 174 | 152 | 347 |
| FY2015 | $80.8M | 202 | 173 | 338 |
| FY2016 | $85.6M | 192 | 169 | 317 |
| FY2017 | $106.2M | 234 | 199 | 325 |
| FY2018 | $102.2M | 240 | 200 | 353 |
| FY2019 | $102.9M | 226 | 199 | 370 |
| FY2020 | $101.2M | 252 | 220 | 403 |
| FY2021 | $121.2M | 283 | 241 | 413 |
| FY2022 | $118.0M | 279 | 245 | 424 |
| FY2023 | $127.2M | 291 | 257 | 414 |
| FY2024 | $127.4M | 290 | 253 | 386 |
| FY2025 | $136.4M | 281 | 238 | 349 |
Where FY2025 money went
| Institution | Obligations | Awards |
|---|---|---|
| Beckman Research Institute/City Of Hope | $9.3M | 15 |
| Sloan-Kettering Inst Can Research | $8.5M | 16 |
| Fred Hutchinson Cancer Center | $8.4M | 6 |
| University Of Pennsylvania | $7.3M | 12 |
| Oregon Health & Science University | $6.0M | 16 |
| Columbia University Health Sciences | $5.5M | 8 |
| University Of Virginia | $5.0M | 7 |
| Washington University | $4.8M | 12 |
| Division Of Cancer Epidemiology And Genetics | $4.5M | 0 |
| Dana-Farber Cancer Inst | $4.0M | 9 |
Text search acute myeloid 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 2026-09-11.
What that buys
Against 127,105 years of life lost a year, FY2025 obligations are $1,073 per life-year — $6,004 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 10 and account for 278 of 281.
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 257 of 281.
Where it lands
Share of $136.4M in FY2025. The top three hold 19%.
Public datasets, ranked
NCBI GEO + Europe PMC + iCite · weekly2,627 human GEO series match acute myeloid leukemia. Keyword relevance cannot tell a 984-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 397-study ranked set
Established
high reuse, older| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE14468 | Gene expression profiling of CEBPA double and single mutant and CEBPA wild type AML.2009 · array | 526 | 152 | 8.8 | patient cohortAPT 0.95survivalmolecularCEBPAFLT3NPM1444 cites |
| GSE37642 | Prognostic gene signature for AML2013 · array | 984 | 284 | 4.1 | patient cohortAPT 0.95survival169 cites |
| GSE18700 | Genome-wide DNA methylation profiling of Acute Myeloid Leukemia2010 · methylation | 352 | 15 | 13.4 | patient cohortAPT 0.95survivalmolecularCEBPANPM1664 cites |
| GSE76009 | A 17-Gene Stemness Score for Rapid Identification of High-Risk AML Patients2016 · array | 534 | 24 | 20.1 | patient cohortAPT 0.95stage730 cites |
| GSE23312 | RUNX1 mutated cases in acute myeloid leukemia share a distinct biological subgroup and are associated with inferior outcome. Results of the AML Study Group (AMLSG).2010 · array | 269 | 6 | 5.7 | patient cohortAPT 0.95survivalmolecularCEBPAIDH1IDH2252 cites |
| GSE71014 | An mRNA Expression Signature for Prognostication in De Novo Acute Myeloid Leukemia Patients with Normal Karyotype2017 · array | 104 | 153 | 2.4 | mixedAPT 0.5survival40 cites |
| GSE63270 | Expression profiles of normal hematopoietic stem and progenitor cells and acute myeloid leukemia sub-populations2016 · array | 104 | 44 | 3.1 | patient cohortAPT 0.5survivalstage124 cites |
| GSE17855 | Expression data from pediatric AML patients2010 · array | 237 | 45 | 2.0 | patient cohortAPT 0.75survival88 cites |
Recent
2022 onward, by score| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE216738 | An inflammatory state remodels the immune microenvironment and improves risk stratification in acute myeloid leukemia2022 · sequencing | 506 | 3 | 13.7 | patient cohortAPT 0.75survival171 cites |
| GSE230559 | Deconvoluting clonal and cellular architecture in IDH-mutant Acute Myeloid Leukemia2025 · single-cell | 130 | 2 | 4.5 | APT 0.75survivalstagemolecularIDH2NPM119 cites |
| GSE296535 | Genetic and Phenotypic correlates of clinical outcomes with Venetoclax in Acute Myeloid Leukemia: The GEN-PHEN-VEN study2025 · single-cell | 6 | 1 | 4.5 | patient cohortAPT 0.75survivalstagemolecularFLT3NPM1TP5317 cites |
| GSE152136 | Subtype-Specific and Structure Variation-Induced Chromatin Spatial Reorganization in Acute Myeloid Leukemia2022 · chromatin | 135 | 7 | 9.3 | APT 0.5171 cites |
| GSE185993 | Longitudinal single-cell profiling of chemotherapy response in acute myeloid leukemia2023 · single-cell | 122 | 7 | 5.1 | APT 0.7566 cites |
| GSE196480 | Mutant NPM1 binds chromatin and directly regulates oncogenic transcription in acute myeloid leukemia2023 · chromatin | 178 | 1 | 10.5 | APT 0.95molecularNPM1130 cites |
Sources: NCBI GEO + Europe PMC + iCite, retrieved 2026-09-11. SubSeries are collapsed to one row per study by linked PMID. Of 705 series retrieved, 17 were dropped by the profile’s exclusion rules and 186 named the disease only in passing. 1 further series named in the profile as contamination are excluded here. 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.
CEBPA
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.
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 (2026-09-11), ClinicalTrials.gov (2026-09-11), openFDA (2026-09-11), NCBI GEO (2026-09-11), PubMed (2026-09-11), NIH RePORTER (2026-09-11).
Negatives stated explicitly
Where nothing exists for acute myeloid 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 THP-1, HL-60 and U937 is used as a model system in innate immunity and macrophage biology (THP-1), neutrophil differentiation (HL-60), infection biology (both). What was removed and why is stated in each section rather than silently applied.
{
"disease": "Acute myeloid leukemia",
"mesh": "Leukemia, Myeloid, Acute",
"facts": "https://usebiotransfer.org/disease/acute-myeloid-leukemia.json",
"methods": "https://usebiotransfer.org/methods/",
"note": "Every figure on the page is in that JSON with its source and retrieval date. Quote from it rather than from the HTML."
}