A randomized phase III study of pretransplant conditioning for AML/MDS with fludarabine and once daily IV busulfan ± clofarabine in allogeneic stem cell transplantation.
Borje S AnderssonPeter F ThallJunsheng MaBenigno C ValdezRoland L BassettJulianne ChenSairah A AhmedAmin M AlousiQaiser BashirStefan CiureaAlison GulbisRita CoolJitesh KawediaChitra HosingPartow KebriaeiSteven Mitchell KornblauAlan MyersBetul OranKatayoun RezvaniNina ShahElizabeth ShpallSimrit ParmarUday R PopatYago NietoRichard E ChamplinPublished in: Bone marrow transplantation (2022)
Pretransplant conditioning with Fludarabine (Flu)-Busulfan (Bu) is safe, but clofarabine (Clo) has improved antileukemic activity. Hypothesis: Flu+Clo-Bu (FCB) yields superior progression-free survival (PFS) after allogeneic transplantation. We randomized 250 AML/MDS patients aged 3-70, Karnofsky Score ≥80, with matched donors, to FCB (n = 120) or Flu-Bu (n = 130), stratifying complete remission (CR) vs. No CR, (NCR). HCT-CI scores varied, from 0 to 10. All evaluable patients engrafted. Median follow-up was 66 months (interquartile range: 58-80). Three-year relapse incidence (RI), 25% with FCB, vs. 39% with Flu-Bu (p = 0.018), offset by higher non-relapse mortality, 22.6% (95%CI: 16-30.2%) vs. 12.3% (95%CI: 6.5-19%). Three-year PFS was 52% (95%CI: 44-62%) (FCB), vs. 48% (95%CI: 41-58%) (Flu-Bu). FCB benefited CR patients less, NCR patients age ≤ 60 had 3-year 34% RI (95%CI: 19-49%) (FCB) vs. 56% (95%CI: 38-70%) after Flu-Bu (p = 0.037). NCR patients >60 years had 3-year RI 10.0% (FCB), vs. 56.0%, after Flu-Bu (p = 0.003). Bayesian regression analysis including treatment-covariate interactions showed FCB superiority in NCR patients with low HCT-CI (0-2). Serious adverse event profiles were similar for the regimens. Conditioning with FCB did not improve PFS overall, but improved disease control in NCR patients, mandating confirmatory trials. Remission status and HCT-CI should be considered when using FCB.
Keyphrases
- end stage renal disease
- stem cell transplantation
- ejection fraction
- newly diagnosed
- chronic kidney disease
- free survival
- clinical trial
- rheumatoid arthritis
- acute myeloid leukemia
- emergency department
- stem cells
- peritoneal dialysis
- high dose
- low dose
- acute lymphoblastic leukemia
- bone marrow
- mesenchymal stem cells
- cell proliferation
- systemic lupus erythematosus
- physical activity
- cardiovascular events
- ulcerative colitis