^
5d
NCI-2020-14163: Seclidemstat and Azacitidine for the Treatment of Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia (clinicaltrials.gov)
P1/2, N=24, Active, not recruiting, M.D. Anderson Cancer Center | Recruiting --> Active, not recruiting | N=44 --> 24
Enrollment closed • Enrollment change
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TP53 (Tumor protein P53) • NRAS (Neuroblastoma RAS viral oncogene homolog) • RUNX1 (RUNX Family Transcription Factor 1) • ASXL1 (ASXL Transcriptional Regulator 1) • SETBP1 (SET Binding Protein 1)
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TP53 mutation • NRAS mutation • ASXL1 mutation
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azacitidine • seclidemstat (SP2577)
6d
Successful Haplo-Hematopoietic Stem Cell Transplantation for Juvenile Myelomonocytic Leukemia in a Child With Underlying Thrombocytopenia-Absent Radius Syndrome: A Unique Case. (PubMed, Cancer Rep (Hoboken))
This case represents, to our knowledge, one of the very few-if not the first-reported instances of successful HSCT for JMML in a patient with TAR syndrome. It underscores the importance of vigilant surveillance in TAR patients for potential malignant transformation and demonstrates the curative potential of HSCT in rare congenital-hematologic overlap syndromes.
Journal
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NF1 (Neurofibromin 1) • RBM8A (RNA Binding Motif Protein 8A)
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RAS mutation
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cyclophosphamide • melphalan • Grafapex (treosulfan)
7d
A phase I open label study of fostamatinib, a SYK inhibitor, in patients with lower-risk myelodysplastic syndrome and chronic myelomonocytic leukemia. (PubMed, Leuk Lymphoma)
Lower-risk myelodysplastic syndromes (MDS) and chronic myelomonocytic leukemia (CMML) are commonly managed with erythropoiesis-stimulating agents, luspatercept, or hypomethylating agents. There were no dose-limiting toxicities. Although safe, fostamatinib demonstrated no clinical benefit, underscoring the need for alternative strategies to modulate inflammatory signaling in MDS/CMML.
P1 data • Journal
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SYK (Spleen tyrosine kinase)
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Reblozyl (luspatercept-aamt) • Tavalisse (fostamatinib)
7d
Low-dose decitabine increases peripheral NKT-like cell proportions in patients with chronic myeloid neoplasms. (PubMed, Cancer Pathog Ther)
Among the three patients who received at least three cycles of decitabine, improvements in anemia and thrombocytopenia were observed in those with elevated NKT-like cell levels. These findings suggest that low-dose decitabine may enhance the NKT-like cell population, which may be associated with therapeutic responses in chronic myeloid neoplasms.
Journal
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CD8 (cluster of differentiation 8) • CD4 (CD4 Molecule)
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decitabine
11d
Enrollment open
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azacitidine • Ojjaara (momelotinib)
11d
BRAF Mutations in Myeloid Neoplasms: Prevalence, Co-Mutation Landscape, and Clinical Outcomes-A Comprehensive Review. (PubMed, Biomedicines)
BRAF mutations in myeloid neoplasms are rare, heterogeneous, and usually represent secondary events in clonal evolution. Although mutation clearance appears prognostically relevant, current targeted approaches provide limited durability, underscoring the need for prospective studies in this setting.
Clinical data • Review • Journal
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BRAF (B-raf proto-oncogene) • DNMT3A (DNA methyltransferase 1) • ASXL1 (ASXL Transcriptional Regulator 1) • TET2 (Tet Methylcytosine Dioxygenase 2) • SRSF2 (Serine and arginine rich splicing factor 2)
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BRAF V600E • BRAF mutation • RAS mutation • ASXL1 mutation • SRSF2 mutation
13d
Impact of High Serum Lysozyme Activity on Renal Function and Survival Outcomes in Transplant-Eligible and Ineligible Acute Myeloid Leukemia. (PubMed, Cancer Med)
After remission induction, most patients with high-lysozyme levels showed creatinine level recovery (AML onset: median 1.15 mg/dL, 1 month later: median 0.72 mg/dL, 3 months later: median 0.65 mg/dL). The effect of lysozyme levels on prognosis is limited because renal function recovers in many patients with high-lysozyme levels after chemotherapy.
Retrospective data • Journal
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LYZ (Lysozyme 2)
15d
CHIS: Clonal Hematopoiesis of Immunological Significance (clinicaltrials.gov)
P=N/A, N=5000, Not yet recruiting, Assistance Publique - Hôpitaux de Paris | N=1000 --> 5000 | Trial primary completion date: Sep 2045 --> Apr 2036
Enrollment change • Trial primary completion date
20d
Enrollment open • Enrollment change
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cyclophosphamide • fludarabine IV • CAR.70/IL15-transduced CB-NK cells
20d
LS1781: Ascorbic Acid and Chemotherapy for the Treatment of Relapsed or Refractory Lymphoma, CCUS, and Chronic Myelomonocytic Leukemia (clinicaltrials.gov)
P2, N=80, Recruiting, Mayo Clinic | Trial completion date: Mar 2027 --> Nov 2033 | Trial primary completion date: Mar 2027 --> Feb 2031
Trial completion date • Trial primary completion date
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IDH1 (Isocitrate dehydrogenase (NADP(+)) 1) • BCL2 (B-cell CLL/lymphoma 2) • IDH2 (Isocitrate Dehydrogenase (NADP(+)) 2) • DNMT3A (DNA methyltransferase 1) • SF3B1 (Splicing Factor 3b Subunit 1) • TET2 (Tet Methylcytosine Dioxygenase 2) • SRSF2 (Serine and arginine rich splicing factor 2) • U2AF1 (U2 Small Nuclear RNA Auxiliary Factor 1) • CD4 (CD4 Molecule) • ZRSR2 (Zinc Finger CCCH-Type, RNA Binding Motif And Serine/Arginine Rich 2)
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IDH2 mutation • TET2 mutation • SF3B1 mutation • EZH2 mutation • SRSF2 mutation
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cisplatin • carboplatin • gemcitabine • Rituxan (rituximab) • cytarabine • cyclophosphamide • ifosfamide • oxaliplatin • etoposide IV • decitabine • Truxima (rituximab-abbs) • Hemady (dexamethasone tablets) • Mabtas (rituximab biosimilar) • Starasid (cytarabine ocfosfate) • dexamethasone injection
20d
ASTX030-01: A Multi-phase Study of ASTX030 (Azacitidine and Cedazuridine) in Myeloid Neoplasm Alone or in Combination With Venetoclax in AML (AZTOUND Study) (clinicaltrials.gov)
P2/3, N=316, Recruiting, Taiho Oncology, Inc. | N=236 --> 316 | Trial completion date: May 2028 --> Nov 2028 | Trial primary completion date: May 2027 --> Nov 2027
Enrollment change • Trial completion date • Trial primary completion date
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Venclexta (venetoclax) • cedazuridine/azacitidine (ASTX030)