Disease Briefing

Acute myeloid 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 2026-09-11Sources Open Targets · ClinicalTrials.gov · openFDA · GEO · PubMed · Europe PMC · iCite · RePORTERRanked 397 studies · 34,772 GEO samples
Reading as
Reorders emphasis only — nothing is hidden or loaded on demand.

Answer block

13 genes recurrently implicated in acute myeloid leukemia — FLT3, NPM1, IDH1, IDH2, KMT2A, MEN1, DNMT3A, TP53, BCL2, CD33, IL3RA, KIT, CEBPA — 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 myeloid leukemia: (Daunorubicin And Cytarabine), Azacitidine, Cedazuridine And Decitabine, Enasidenib, Gemtuzumab Ozogamicin, Gilteritinib and 11 more. This counts labels, not treatment — the disease is also treated with agents approved under broader indications
8
of the 13 genes above carry a drug that is approved in acute myeloid leukemia itself — BCL2, CD33, DNMT3A, FLT3, IDH1, IDH2, KIT, MEN1. Across all of them 130 drug entries reach these genes, 112 distinct once salt forms are merged
36
registered CD33 cell-therapy trials in acute myeloid leukemia, 16 active and 2 withdrawn. Counted from ClinicalTrials.gov across 6 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
1
target carries an Open Targets tractability signal and has no clinical programme of any kind: CEBPA. FLT3, CD33, IL3RA all have cell-therapy trials, so they are undrugged rather than untouched
2,627
human GEO series match the disease; 397 survive on-topic filtering, and only 60 are patient cohorts of 100+ samples
284
Europe PMC full-text papers name GSE37642 — the highest accession-mention count in the set. A mention is not proof of reanalysis, so read it as reach rather than reuse
$136.4M
NIH obligations in FY2025, up 129% since 2013 — while distinct core projects went 139 to 238. Both more projects (+71%) and larger awards, the latter carrying more of the growth; core projects are not the same unit as laboratories

Target landscape

Open Targets · retrieved 2026-09-11 · weekly

13 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.

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
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 · weekly

17 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.

17Labelled for acute myeloid leukemiaFDA INDICATIONS AND USAGE names the disease
24Approved, but for another diseasereturned for the genes in the table above
1Backbone agents listing itbroad cytotoxics whose labels name many tumours
16Active CD33 cell-therapy trialsof 36 registered

Every label that names acute myeloid leukemia

DrugRoleWhat the label says
(Daunorubicin And Cytarabine)VYXEOSLabelled hereVYXEOS 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.
AzacitidineONUREGLabelled hereONUREG 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 DecitabineINQOVILabelled hereAcute 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.
EnasidenibIdhifaLabelled hereAcute 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 OzogamicinMylotargLabelled hereNewly-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.
GilteritinibXospataLabelled hereRelapsed 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.
GlasdegibDaurismoLabelled hereDAURISMO 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 HydrochlorideLabelled hereIDAMYCIN PFS is indicated for the treatment of adult patients with acute myeloid leukemia (AML) as a component of a combination chemotherapy regimen.
IvosidenibTIBSOVOLabelled hereNewly 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...
OlutasidenibREZLIDHIALabelled hereRelapsed 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
QuizartinibVANFLYTALabelled hereVANFLYTA 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.
RevumenibRevuforjLabelled 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.
RydaptRYDAPTLabelled hereAcute 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
SargramostimLeukineLabelled hereAcute 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).
TreosulfanGRAFAPEXLabelled hereAcute 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).
VenetoclaxVenclextaLabelled hereAcute 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.
ZiftomenibKomziftiLabelled hereKOMZIFTI 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, NYPOZIBackbonePatients 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 · weekly

CD33 is the busiest cell-therapy antigen in acute myeloid leukemia: 36 registered trials, 16 still active, 2 withdrawn before enrolling anyone.

TrialPhaseStatusTitleLast update
NCT064200631/2RecruitingSequential CAR-T Cells Targeting CD33/CD123 in Patients With Acute Myelocytic Leukemia AML2024-11-12
NCT06762132EARLY/1RecruitingA Clinical Study to Explore the Safety and Efficacy of CD33 CAR-T Cell in Relapsed/Refractory Acute Myeloid Leukemia2025-01-07
NCT051051521RecruitingPLAT-08: A Study Of SC-DARIC33 CAR T Cells In Pediatric And Young Adults With Relapsed Or Refractory CD33+ AML2025-12-23
NCT056721471RecruitingCD33-CAR T Cell Therapy for the Treatment of Recurrent or Refractory Acute Myeloid Leukemia2026-03-05
NCT075235551/2RecruitingAdaptive Dual-Target CAR-T Cells for Relapsed or Refractory Hematologic Malignancies2026-04-13
NCT063260211RecruitingOptimised CD33 (FL-33) CAR T Therapy for Refractory/Relapsed Acute Myeloid Leukaemia2026-05-22
NCT076685571RecruitingAnti-CD33-CLL1 CAR-T Cells (ICG415) for the Treatment of Relapsed/Refractory Acute Myeloid Leukemia2026-06-25
NCT059458491RecruitingCD33KO-HSPC Infusion Followed by CART-33 Infusion(s) for Refractory/Relapsed AML2026-07-09
NCT039272611ActivePRGN-3006 Adoptive Cellular Therapy for CD33-Positive Relapsed or Refractory AML, MRD Positive AML or Higher Risk MDS2024-11-08
NCT039717991/2ActiveStudy of Anti-CD33 Chimeric Antigen Receptor-Expressing T Cells (CD33CART) in Children and Young Adults With Relapsed/Refractory Acute Myeloid Leukemia2025-07-14

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 · monthly

Every 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 term2015–182021–25ChangeShare now
Receptors, Chimeric Antigen0.08%1.52%18.18×91 papers
Bridged Bicyclo Compounds, Heterocyclic0.62%7.65%12.4×459 papers
Sulfonamides1.03%7.82%7.56×469 papers
RNA, Circular0.08%0.62%7.39×37 papers
Aniline Compounds0.25%1.18%4.73×71 papers
Pyrazines0.25%1.12%4.47×67 papers
Inflammation0.15%0.58%3.89×35 papers
Tumor Microenvironment1.02%3.78%3.72×227 papers
Molecular Docking Simulation0.23%0.8%3.43×48 papers
Myeloproliferative Disorders0.63%2.03%3.21×122 papers

Cooling

MeSH term2015–182021–25ChangeShare now
Survival Analysis6.57%0.65%0.1×39 papers
Real-Time Polymerase Chain Reaction2.0%0.2%0.1×12 papers
Biopsy1.62%0.22%0.13×13 papers
Gene Expression2.63%0.33%0.13×20 papers
Kaplan-Meier Estimate3.87%0.53%0.14×32 papers
Tumor Cells, Cultured3.45%0.47%0.14×28 papers

Biggest topics now

MeSH term2015–182021–25ChangeShare now
Mutation15.68%17.37%1.11×1042 papers
Prognosis18.27%17.17%0.94×1030 papers
Hematopoietic Stem Cell Transplantation12.4%13.88%1.12×833 papers
Antineoplastic Combined Chemotherapy Protocols13.68%11.58%0.85×695 papers
Apoptosis8.67%8.33%0.96×500 papers
Myelodysplastic Syndromes8.73%8.25%0.94×495 papers
Antineoplastic Agents12.97%8.0%0.62×480 papers
Sulfonamides1.03%7.82%7.56×469 papers
Bridged Bicyclo Compounds, Heterocyclic0.62%7.65%12.4×459 papers
Treatment Outcome14.07%7.48%0.53×449 papers

Publication mix

Type2015–182021–25
Clinical Trial0.1%0.1%
Randomized Controlled Trial1.9%1.2%
Review11.8%10.1%
Meta-Analysis0.7%0.7%
Case Reports0.0%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.

MeasureValueMatchWhat it counts
New cases each year22,720 cases/yeardirect2026
Deaths each year11,500 deaths/yeardirect2026
Incidence rate4.4 cases per 100,000 per yeardirect2019-2023
Death rate2.7 deaths per 100,000 per yeardirect2020-2024
People living with it83,311 people living with the diseasedirect2023
Median age at diagnosis70.0 yearsdirect2019-2023
median age at death74 yearsdirect2020-2024
Five-year relative survival33.4%direct2016-2022

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 · quarterly

NIH 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.

$136.4MNIH obligations, FY2025from $59.6M in FY2013 · +129%
238distinct projects funded139 in FY2013
$136.4Mpeak year was FY2025obligations, all institutes
91%of FY2025 awards from NCI252 of 278

NIH obligations by fiscal year

$34M$68M$102M$136M13151719212325
YearObligationsAwardsDistinct projectsDropped as off-topic
FY2013$59.6M161139346
FY2014$69.1M174152347
FY2015$80.8M202173338
FY2016$85.6M192169317
FY2017$106.2M234199325
FY2018$102.2M240200353
FY2019$102.9M226199370
FY2020$101.2M252220403
FY2021$121.2M283241413
FY2022$118.0M279245424
FY2023$127.2M291257414
FY2024$127.4M290253386
FY2025$136.4M281238349

Where FY2025 money went

InstitutionObligationsAwards
Beckman Research Institute/City Of Hope$9.3M15
Sloan-Kettering Inst Can Research$8.5M16
Fred Hutchinson Cancer Center$8.4M6
University Of Pennsylvania$7.3M12
Oregon Health & Science University$6.0M16
Columbia University Health Sciences$5.5M8
University Of Virginia$5.0M7
Washington University$4.8M12
Division Of Cancer Epidemiology And Genetics$4.5M0
Dana-Farber Cancer Inst$4.0M9

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

NCI252 · 90%
NHLBI9 · 3%
VA6 · 2%
NIA3 · 1%
FDA3 · 1%
NIMHD1 · 0%

Projects by administering institute. The rows above are the top 10 and account for 278 of 281.

Award mechanisms

R01135 · 48%
P0121 · 7%
R3718 · 6%
K0814 · 5%
U5411 · 4%
F309 · 3%

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

Beckman Research Institute/City Of Hope$9.3M · 6.8%
Sloan-Kettering Inst Can Research$8.5M · 6.3%
Fred Hutchinson Cancer Center$8.4M · 6.1%
University Of Pennsylvania$7.3M · 5.3%
Oregon Health & Science University$6.0M · 4.4%
Columbia University Health Sciences$5.5M · 4.1%

Share of $136.4M in FY2025. The top three hold 19%.

Public datasets, ranked

NCBI GEO + Europe PMC + iCite · weekly

2,627 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

patient 137unspecified 99mixed 93cell line 62xenograft 6
137 patient99 unspecified93 mixed62 cell line6 xenograft223 carry clinical annotation156 carry survival60 patient cohorts ≥100 GEO samples34,772 GEO samples totalin 28 single-cell series a GEO sample is one cell, not one patient

Established

high reuse, older
AccessionStudySamplesMentionsEurope PMCRCREvidence
GSE14468Gene expression profiling of CEBPA double and single mutant and CEBPA wild type AML.2009 · array5261528.8
patient cohortAPT 0.95survivalmolecularCEBPAFLT3NPM1444 cites
GSE37642Prognostic gene signature for AML2013 · array9842844.1
patient cohortAPT 0.95survival169 cites
GSE18700Genome-wide DNA methylation profiling of Acute Myeloid Leukemia2010 · methylation3521513.4
patient cohortAPT 0.95survivalmolecularCEBPANPM1664 cites
GSE76009A 17-Gene Stemness Score for Rapid Identification of High-Risk AML Patients2016 · array5342420.1
patient cohortAPT 0.95stage730 cites
GSE23312RUNX1 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 · array26965.7
patient cohortAPT 0.95survivalmolecularCEBPAIDH1IDH2252 cites
GSE71014An mRNA Expression Signature for Prognostication in De Novo Acute Myeloid Leukemia Patients with Normal Karyotype2017 · array1041532.4
mixedAPT 0.5survival40 cites
GSE63270Expression profiles of normal hematopoietic stem and progenitor cells and acute myeloid leukemia sub-populations2016 · array104443.1
patient cohortAPT 0.5survivalstage124 cites
GSE17855Expression data from pediatric AML patients2010 · array237452.0
patient cohortAPT 0.75survival88 cites

Recent

2022 onward, by score
AccessionStudySamplesMentionsEurope PMCRCREvidence
GSE216738An inflammatory state remodels the immune microenvironment and improves risk stratification in acute myeloid leukemia2022 · sequencing506313.7
patient cohortAPT 0.75survival171 cites
GSE230559Deconvoluting clonal and cellular architecture in IDH-mutant Acute Myeloid Leukemia2025 · single-cell13024.5
APT 0.75survivalstagemolecularIDH2NPM119 cites
GSE296535Genetic and Phenotypic correlates of clinical outcomes with Venetoclax in Acute Myeloid Leukemia: The GEN-PHEN-VEN study2025 · single-cell614.5
patient cohortAPT 0.75survivalstagemolecularFLT3NPM1TP5317 cites
GSE152136Subtype-Specific and Structure Variation-Induced Chromatin Spatial Reorganization in Acute Myeloid Leukemia2022 · chromatin13579.3
APT 0.5171 cites
GSE185993Longitudinal single-cell profiling of chemotherapy response in acute myeloid leukemia2023 · single-cell12275.1
APT 0.7566 cites
GSE196480Mutant NPM1 binds chromatin and directly regulates oncogenic transcription in acute myeloid leukemia2023 · chromatin178110.5
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 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.

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

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.

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."
}