A phase II study of azacitidine in combination with granulocyte-macrophage colony-stimulating factor as maintenance treatment, after allogeneic blood or marrow transplantation in patients with poor-risk acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS).
Jonathan A WebsterMeera YogarajahMarianna ZahurakHeather SymonsAmy E DezernIvana GojoGabrielle T PrinceJillian MorrowRichard J JonesB Douglas SmithMargaret ShowelPublished in: Leukemia & lymphoma (2021)
Relapse is the most common cause of treatment failure following allogeneic blood or marrow transplantation (alloBMT) for AML or MDS. Post-transplant maintenance therapies may prevent relapse. We conducted a phase II trial combining azacitidine (AZA) with GM-CSF in non-relapsed, post-transplant patients with AML or MDS. Patients received escalating doses of AZA to a maximum of 75 mg/m2 for 5 days per cycle for up to 12 cycles. GM-CSF was given on days 1-10 of each cycle. Eighteen patients were treated following non-myeloablative (17) and myeloablative (1) alloBMT for AML (61.1%), MDS (27.7%), or therapy-related myeloid neoplasm (11.1%). The majority of patients (72%) received their graft from an HLA-haploidentical donor. The treatment was well-tolerated with rare grade 3-4 hematologic toxicities. One patient suffered an exacerbation of GVHD. The 24-month relapse-free and overall survivals were 47 and 57%, respectively, with a median of 18.6 and 29 months.
Keyphrases
- acute myeloid leukemia
- allogeneic hematopoietic stem cell transplantation
- end stage renal disease
- stem cell transplantation
- newly diagnosed
- chronic kidney disease
- ejection fraction
- bone marrow
- stem cells
- acute lymphoblastic leukemia
- patient reported outcomes
- peritoneal dialysis
- dendritic cells
- high dose
- mesenchymal stem cells
- case report
- clinical trial
- open label
- acute respiratory distress syndrome
- diffuse large b cell lymphoma
- multiple myeloma
- peripheral blood
- cell therapy
- high grade
- low grade
- replacement therapy
- cerebrospinal fluid