Acute leukemia of ambiguous lineage
diseaseOn this page
Also known as acute leukaemia of indeterminate lineageacute leukaemia of undetermined lineageacute leukemia of indeterminate lineageacute leukemia of undetermined lineageALL with myeloid markersAML with lymphoid markersBALbiphenotypic acute leukaemiabiphenotypic acute leukemiahybrid acute leukaemiahybrid acute leukemiamixed lineage acute leukaemiamixed lineage acute leukemiamixed phenotype acute leukaemia
Summary
Acute leukemia of ambiguous lineage (MONDO:0019460) is a cancer and 34 clinical trials. Top therapeutic interventions include revumenib, calaspargase pegol, and dexrazoxane. A subtype of acute myeloid leukemia — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Classification: Cancer
- ClinVar variants: 1
- Clinical trials: 34
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | acute leukemia of ambiguous lineage |
| Mondo ID | MONDO:0019460 |
| Orphanet | 86851 |
| ICD-11 | 1062906118 |
| NCIT | C7464 |
| SNOMED CT | 721308005 |
| UMLS | C1301357 |
| MedGen | 226983 |
| GARD | 0008638 |
| MedDRA | 10067399 |
| Is cancer (heuristic) | yes |
Also known as: acute leukaemia of indeterminate lineage · acute leukaemia of undetermined lineage · acute leukemia of ambiguous lineage · acute leukemia of indeterminate lineage · acute leukemia of undetermined lineage · ALL with myeloid markers · AML with lymphoid markers · BAL · biphenotypic acute leukaemia · biphenotypic acute leukemia · hybrid acute leukaemia · hybrid acute leukemia · mixed lineage acute leukaemia · mixed lineage acute leukemia · mixed phenotype acute leukaemia
Data availability: 1 ClinVar variant · 1 cell line.
Disease family
This is a subtype of acute myeloid leukemia. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.
Classification path: human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › hematopoietic and lymphoid system neoplasm › hematopoietic and lymphoid cell neoplasm › leukemia › myeloid leukemia › acute myeloid leukemia › acute leukemia of ambiguous lineage
Related subtypes (77): childhood acute myeloid leukemia, acute monocytic leukemia, acute myeloid leukemia with t(8;21)(q22;q22) translocation, acute myeloid leukemia by FAB classification, inherited acute myeloid leukemia, acute myeloid leukemia with CEBPA somatic mutations, acute myeloid leukemia with t(8;16)(p11;p13) translocation, acute myeloid leukemia with t(6;9)(p23;q34), acute myeloid leukemia with t(9;11)(p22;q23), acute myeloid leukemia with inv3(p21;q26.2) or t(3;3)(p21;q26.2), megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13), acute myeloid leukemia with NPM1 somatic mutations, acute myeloid leukemia with multilineage dysplasia, therapy related acute myeloid leukemia and myelodysplastic syndrome, acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22), acute myeloid leukemia with 11q23 abnormalities, acute myeloid leukemia with BCR-ABL1, acute myeloid leukemia with mutated NPM1, acute myeloid leukemia, inv(16)(p13.1;q22), acute myeloid leukemia, t(16;16)(p13.1;q22), acute myeloid leukemia, t(15;17)(q24;q21), acute myeloid leukemia, t(9;11)(p21.3;q23.3), acute myeloid leukemia, t(10;11)(p12;q23), acute myeloid leukemia, t(10;11)(p11.2;q23), acute myeloid leukemia, t(1;11)(q21;q23), acute myeloid leukemia, t(4;11)(q21;q23), acute myeloid leukemia, t(6;11)(q27;q23), acute myeloid leukemia, t(6;9)(p23;q34.1), acute myeloid leukemia, t(11;19)(q23;p13), acute myeloid leukemia, t(11;19)(q23;p13.1), acute myeloid leukemia, t(11;19)(q23.3;p13.3), acute myeloid leukemia, t(v;11q23.3), acute myeloid leukemia, Monosomy 7, acute myeloid leukemia, Monosomy 5, acute myeloid leukemia, Trisomy 8, acute myeloid leukemia, der12p, acute myeloid leukemia, t(2;12), acute myeloid leukemia, t(11;17), acute myeloid leukemia, t(8;16), acute myeloid leukemia, t(1;22), acute myeloid leukemia, t(5;11)(q35;p15), acute myeloid leukemia, t(7;12)(q36;p13), acute myeloid leukemia, t(9;22)(q34.1;q11.2), acute myeloid leukemia, inv(3)(q21.3;q26.2), acute myeloid leukemia, t(3;3)(q21.3;q26.2), acute myeloid leukemia, t(3;12)(q23;p12.3), acute myeloid leukemia, del(5q31-q32), acute myeloid leukemia, del(13q14-q21), acute myeloid leukemia, loss of chromosome 17p, acute myeloid leukemia, MLL gene rearrangement, acute myeloid leukemia, Non-KMT2A MLLT10 rearrangement positive, acute myeloid leukemia, inv(16)(p13.3;q24.3), acute myeloid leukemia, t(11;15)(p15;q35), acute myeloid leukemia, t(16;21)(q24;q22), acute myeloid leukemia, t(3;5)(q25;q34), acute myeloid leukemia, t(16;21)(p11;q22), acute myeloid leukemia, monoallelic CEBPA gene mutation, acute myeloid leukemia, biallelic CEBPA gene mutation, acute myeloid leukemia, CEBPA gene mutation, acute myeloid leukemia, FLT3 internal tandem duplication, acute myeloid leukemia, FLT3 tyrosine kinase domain point mutation, acute myeloid leukemia, WT1 gene mutation, acute myeloid leukemia, KIT exon 17 mutation, acute myeloid leukemia, KIT exon 8 mutation, acute myeloid leukemia, KIT gene mutation, acute myeloid leukemia, GATA1 gene mutation, acute myeloid leukemia, RUNX1 gene mutation, acute myeloid leukemia, PTPN11 gene mutation, acute myeloid leukemia, NRAS gene mutation, acute myeloid leukemia, KRAS gene mutation, core binding factor acute myeloid leukemia, acute myeloid leukemia, t(8;21)(q22; q22.1), acute myeloid leukemia, t(1;22)(p13;q13), acute myeloid leukemia with CBFA2T3-GLIS2 fusion, acute myeloid leukemia with FUS-ERG fusion, acute myeloid leukemia with MNX1-ETV6 fusion, acute myeloid leukemia with NPM1-MLF1 fusion
Subtypes (3): bilineal acute myeloid leukemia, acute undifferentiated leukemia, mixed phenotype acute leukemia
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
ClinVar germline variants
1 retrieved; paginated sample, class counts are floors:
1 conflicting classifications of pathogenicity
| ClinVar | Variant (HGVS) | Gene | Classification | Review |
|---|---|---|---|---|
| 2232 | NM_000551.4(VHL):c.598C>T (p.Arg200Trp) | LOC107303340 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications |
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 34.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| PHASE2 | 20 |
| PHASE1 | 6 |
| Not specified | 3 |
| PHASE2/PHASE3 | 2 |
| PHASE1/PHASE2 | 2 |
| PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT05515029 | PHASE3 | ACTIVE_NOT_RECRUITING | Preventing of GVHD With Post-transplantation Cyclophosphamide, Abatacept, Vedolizumab and Calcineurin Inhibitor at Patients With Hemoblastosis |
| NCT06475820 | PHASE2/PHASE3 | ACTIVE_NOT_RECRUITING | Preventing of GVHD With Post-transplantation Cyclophosphamide, Abatacept, Vedolizumab and Baricitinib at Children and Young Adults With Hemoblastosis |
| NCT06756152 | PHASE2/PHASE3 | RECRUITING | Preventing of GVHD with Post-transplantation Cyclophosphamide, Abatacept, Vedolizumab and Ruxolitinib At Children and Young Adults with Hemoblastosis |
| NCT03779854 | PHASE2 | RECRUITING | Naive T Cell Depletion for Preventing Chronic Graft-versus-Host Disease in Children and Young Adults With Blood Cancers Undergoing Donor Stem Cell Transplant |
| NCT04065399 | PHASE1/PHASE2 | RECRUITING | A Study of Revumenib in R/R Leukemias Including Those With an MLL/KMT2A Gene Rearrangement or NPM1 Mutation |
| NCT04067336 | PHASE1/PHASE2 | ACTIVE_NOT_RECRUITING | First in Human Study of Ziftomenib in Relapsed or Refractory Acute Myeloid Leukemia |
| NCT04440267 | PHASE2 | RECRUITING | Efficacy of Acute Lymphoblastic Leukemia-Based Therapy in Treating Patients With Acute Leukemia of Ambiguous Lineage |
| NCT05761171 | PHASE2 | ACTIVE_NOT_RECRUITING | A Study of Revumenib in Combination With Chemotherapy for Patients Diagnosed With Relapsed or Refractory Leukemia |
| NCT05805605 | PHASE2 | RECRUITING | Allo HSCT Using RIC and PTCy for Hematological Diseases |
| NCT05901974 | PHASE2 | RECRUITING | Venetoclax Combined With Azactidine in the Treatment of ALAL |
| NCT06013423 | PHASE2 | RECRUITING | Cord Blood Transplant, Cyclophosphamide, Fludarabine, and Total-Body Irradiation in Treating Patients With High-Risk Hematologic Diseases |
| NCT06317662 | PHASE2 | RECRUITING | Testing the Addition of the Anti-cancer Drug Venetoclax and/or the Anti-cancer Immunotherapy Blinatumomab to the Usual Chemotherapy Treatment for Infants With Newly Diagnosed KMT2A-rearranged or KMT2A-non-rearranged Leukemia |
| NCT06355583 | PHASE2 | RECRUITING | Intestinal Microbiota Transplant Prior to Allogeneic Stem Cell Transplant (MAST) Trial |
| NCT06477549 | PHASE2 | RECRUITING | BeFluBu vs FluBuRux Conditioning in Haploidentical HCT |
| NCT06508099 | PHASE2 | RECRUITING | Vitamin A and D Supplementation in Allogeneic HCT |
| NCT07046078 | PHASE2 | RECRUITING | Combination Chemotherapy (FLAG-Ida) Followed Immediately by Reduced-Intensity Total Body Radiation Therapy and Donor Hematopoietic Cell Transplant for the Treatment of Adults Age 60 and Older With Newly Diagnosed Adverse-Risk Acute Myeloid Leukemia or Other High-Grade Myeloid Cancer |
| NCT00863148 | PHASE2 | COMPLETED | Allogeneic Stem Cell Transplant With Clofarabine, Busulfan and Antithymocyte Globulin (ATG) for Adult Patients With High-risk Acute Myeloid Leukemia/Myelodysplastic Syndromes (AML/MDS) or Acute Lymphoblastic Leukemia (ALL) |
| NCT01858740 | PHASE2 | COMPLETED | Selective Depletion of CD45RA+ T Cells From Allogeneic Peripheral Blood Stem Cell Grafts in Preventing GVHD in Children |
| NCT02135874 | PHASE2 | COMPLETED | Clofarabine, Idarubicin, Cytarabine, Vincristine Sulfate, and Dexamethasone in Treating Patients With Newly Diagnosed or Relapsed Mixed Phenotype Acute Leukemia |
| NCT02220985 | PHASE2 | COMPLETED | Selective Depletion of CD45RA+ T Cells From Allogeneic Peripheral Blood Stem Cell Grafts From HLA-Matched Related and Unrelated Donors in Preventing GVHD |
| NCT02419755 | PHASE2 | TERMINATED | Bortezomib and Vorinostat in Younger Patients With Refractory or Relapsed MLL Rearranged Hematologic Malignancies |
| NCT02828358 | PHASE2 | COMPLETED | Azacitidine and Combination Chemotherapy in Treating Infants With Acute Lymphoblastic Leukemia and KMT2A Gene Rearrangement |
| NCT03012672 | PHASE2 | COMPLETED | Higher or Lower Dose Cladribine, Cytarabine, and Mitoxantrone in Treating Medically Less Fit Patients With Newly Diagnosed Acute Myeloid Leukemia or Myeloid Neoplasm |
| NCT04191187 | PHASE2 | COMPLETED | Reduced Intensity Flu/Mel/TBI Conditioning for HAPLO HCT Patients With Hematologic Malignancies |
| NCT04942730 | PHASE2 | COMPLETED | Benadamustine, Fludarabine and Busulfan Conditioning in Recipients of Haploidentical Stem Cell Transplantation (FluBuBe) |
| NCT05292664 | PHASE1 | RECRUITING | Venetoclax Basket Trial for High Risk Hematologic Malignancies |
| NCT06177067 | PHASE1 | RECRUITING | Study of Revumenib, Azacitidine, and Venetoclax in Pediatric and Young Adult Patients With Refractory or Relapsed Acute Myeloid Leukemia |
| NCT06575296 | PHASE1 | RECRUITING | Revumenib for the Treatment of Acute Leukemia in Patients Post-Allogeneic Stem Cell Transplant |
| NCT01319864 | PHASE1 | COMPLETED | POETIC Plerixafor as a Chemosensitizing Agent for Relapsed Acute Leukemia and MDS in Pediatric Patients |
| NCT01701323 | PHASE1 | TERMINATED | Expanded Cord Blood Cell Infusion Following Combination Chemotherapy in Younger Patients With Relapsed or Refractory Acute Myeloid Leukemia |
| NCT05521087 | PHASE1 | WITHDRAWN | A Study of JNJ-75276617 in Combination With Conventional Chemotherapy for Pediatric and Young Adult Participants With Relapsed/Refractory Acute Leukemias |
| NCT05794880 | Not specified | RECRUITING | MCW Alpha/Beta T-Cell and B-Cell Depletion With Targeted ATG Dosing |
| NCT07094750 | Not specified | NOT_YET_RECRUITING | Randomization for the Identification of Best Treatment Intensity for Less Fit Adults With Acute Myeloid Leukemia and Myeloid Neoplasms |
| NCT02551718 | Not specified | COMPLETED | High Throughput Drug Sensitivity Assay and Genomics- Guided Treatment of Patients With Relapsed or Refractory Acute Leukemia |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| REVUMENIB | 4 | 4 |
| CALASPARGASE PEGOL | 4 | 3 |
| DEXRAZOXANE | 4 | 3 |
| ASPARAGINASE | 4 | 2 |
| BENDAMUSTINE HYDROCHLORIDE | 4 | 2 |
| DAUNORUBICIN | 4 | 2 |
| HYDROCORTISONE SODIUM SUCCINATE | 4 | 2 |
| MITOXANTRONE | 4 | 2 |
| THIOGUANINE | 4 | 2 |
| ABATACEPT | 4 | 1 |
| ASPARAGINASE ERWINIA CHRYSANTHEMI | 4 | 1 |
| BARICITINIB | 4 | 1 |
| BLINATUMOMAB | 4 | 1 |
| CLADRIBINE | 4 | 1 |
| CLOFARABINE | 4 | 1 |
| COBICISTAT | 4 | 1 |
| ITRACONAZOLE | 4 | 1 |
| LEVOLEUCOVORIN | 4 | 1 |
| PEGASPARGASE | 4 | 1 |
| RETINOL | 4 | 1 |
| SORAFENIB | 4 | 1 |
| VEDOLIZUMAB | 4 | 1 |
| ZIFTOMENIB | 1 | 1 |
| CHEMBL5427854 | 0 | 1 |
| CHEMBL4776881 | 0 | 1 |
| HYOSCYAMINE | -1 | 1 |
Related Atlas pages
- Drugs: Revumenib, Calaspargase Pegol, Dexrazoxane, Asparaginase, Bendamustine, Daunorubicin, Hydrocortisone, Mitoxantrone, Thioguanine, Abatacept, Asparaginase Erwinia Chrysanthemi, Baricitinib, Blinatumomab, Cladribine, Clofarabine, Cobicistat, Itraconazole, Levoleucovorin, Pegaspargase, Retinol, Sorafenib, Vedolizumab, Hyoscyamine