Background The relapse rate remains high in patients with myelodysplastic syndrome (MDS)-refractory anemia with excess blasts (RAEB) and secondary acute myeloid leukemia evolving from MDS (sAML) undergoing allogeneic hematopoietic cell transplantation (allo-HCT). We investigated whether the addition of granulocyte colony-stimulating factor (G-CSF) and decitabine to busulfan plus cyclophosphamide (BuCy) conditioning would reduce relapse in this population.

Methods We did an open-label, randomised phase 3 trial at six hospitals in China. Eligible patients (aged 14-65 years) had a diagnosis of MDS-RAEB or sAML, were willing to undergo allo-HCT, and had an Eastern Cooperative Oncology Group performance status of 0-2 and HCT-comorbidity index of 0-2. Patients were randomly assigned 1:1 to receive G-CSF and decitabine plus BuCy (G-DAC-BuCy) or BuCy conditioning. Randomisation was done with permuted blocks (block size four) and implemented through an interactive web-based randomisation system. The primary endpoint was the 2-year cumulative incidence of relapse (CIR) in the intention-to-treat population. This trial is registered with ClinicalTrials.gov, NCT02744742.

Findings Between April 18, 2016 and September 30, 2019, 202 patients were enrolled and randomly assigned to receive G-DAC-BuCy (n=101) or BuCy conditioning (n=101). Median follow-up was 32.4 (range, 1.0-64.5) months after randomization. The 2-year CIR was 10.9% (95% CI: 5.8-17.9%) and 24.8% (16.8-33.5%) in the G-DAC-BuCy and BuCy groups (HR=0.387, 95% CI: 0.190-0.786; P=0.011). Within 100 days post-transplantation, the most common grade 3-4 adverse effects (AEs) in the G-DAC-BuCy and BuCy groups were infections (34 [33.7%] and 32 [31.7%]), acute graft-versus-host disease (30 [29.7%] and 30 [29.7%]), and gastrointestinal toxicity (28 [27.7%] and 29 [28.7%]). Eleven patients in the G-DAC-BuCy and 13 in the BuCy group died of AEs.

Interpretation G-DAC-BuCy conditioning can prevent relapse compared with BuCy conditioning and is well tolerated, suggesting its potential to become a standard conditioning in patients with MDS-RAEB and sAML undergoing allo-HCT.

No relevant conflicts of interest to declare.

Author notes

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Asterisk with author names denotes non-ASH members.

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