Reduced intensity versus myeloablative conditioning for MDS: long-term results of an EBMT phase III study (RICMAC).
Christian NiederwieserSimona IacobelliGeorg-Nikolaus FrankeLinda KosterMarleen van OsUwe PlatzbeckerKai HübelChristof ScheidLutz Peter MüllerMatthias StelljesElena MorozovaJakob R PasswegFrancesco OnidaPeter DregerRiccardo SaccardiMarco LadettoUrpu SalmenniemiWolfgang Andreas BethgeXavier PoiréGuido KobbeDonal P McLornanMarie RobinNicolaus KrögerPublished in: Bone marrow transplantation (2024)
Short-term outcome of myeloablative (MAC) and reduced intensity (RIC) conditioning in the prospective randomized international EBMT RICMAC study in patients with myelodyplastic syndrome (MDS) was comparable but longer follow up is lacking. Patients with MDS aged 18-65 years were randomized to receive MAC (N = 64) with busulfan/cyclophosphamide or RIC (n = 65) with busulfan/fludarabine followed by stem cell transplantation -(HCT) from HLA matched or mismatched donor. After a median follow-up of 6.2 (0.4-12.5) years, 10-year OS and RFS were 54.0% and 43.9% for RIC and 44.4% and 44.2% for MAC (p = 0.15 and p = 0.78), respectively. Since the first report, 6 patients died on NRM, 4 after RIC, and 2 after MAC. Similarly, 8 patients relapsed (4 in each arm), increasing the number of relapsed patients to 28. The second HCT was performed in 18 pts, 8 in the MAC, and 10 in the RIC arm. In a multivariate analysis, ECOG status and chemotherapy prior to HCT were independent risk factors for OS and RFS, ECOG and low cytogenetic risk for NRM and chemotherapy prior to HCT for RI. Patients with low cytogenetic risk had better OS [p = 0.002], RFS [p = 0.02], and NRM (p = 0.015) after RIC as compared to MAC.
Keyphrases
- stem cell transplantation
- end stage renal disease
- phase iii
- chronic kidney disease
- newly diagnosed
- ejection fraction
- open label
- high dose
- clinical trial
- acute lymphoblastic leukemia
- double blind
- randomized controlled trial
- allogeneic hematopoietic stem cell transplantation
- acute myeloid leukemia
- diffuse large b cell lymphoma
- radiation therapy
- squamous cell carcinoma
- cell proliferation
- multiple myeloma
- data analysis