Conditioning therapy with N‐acetyl‐L‐cysteine, decitabine and modified BUCY regimen for myeloid malignancies patients prior to allogeneic hematopoietic stem cell transplantation

癸他滨 医学 养生 骨髓增生异常综合症 造血干细胞移植 内科学 髓系白血病 髓样 移植 造血细胞 阿扎胞苷 调理疗法 造血 癌症研究 干细胞 肿瘤科 骨髓 生物 DNA甲基化 基因表达 基因 生物化学 遗传学
作者
Yaqiong Tang,Ziyan Zhang,Silu Liu,Yifang Yao,Tingting Pan,Jiaqian Qi,Huizhu Kang,Yuejun Liu,Chengsen Cai,Meng Zhou,Xuefeng He,Xiaohui Hu,Xiao Ma,Depei Wu,Yue Han
出处
期刊:American Journal of Hematology [Wiley]
卷期号:98 (6): 881-889
标识
DOI:10.1002/ajh.26903
摘要

Conditioning therapy is an essential procedure prior to hematopoietic stem cell transplant (HSCT), imposing a great impact on the outcomes of recipients. We performed a prospective randomized controlled trial to assess the outcome of HSCT recipients with myeloid malignancies after receiving the conditioning therapy consisting of modified BUCY (mBUCY), N-acetyl-L-cysteine (NAC), and decitabine. Enrolled patients were randomly allocated to either Arm A (decitabine, day -12 to -10; NAC, day -9 to +30; mBUCY, day -9 to -2), or Arm B (mBUCY regimen followed by stem cells infusion). Seventy-six patients in Arm A and 78 patients in Arm B were finally evaluated. The results showed platelet recovery accelerate in Arm A, with more patients achieving a platelet count of ≥50 × 109 /L than Arm B at day +30 and +60 (p = .004 and .043, respectively). The cumulative incidence of relapse is 11.8% (95% CI 0.06-0.22) in Arm A, and 24.4% (95% CI 0.16-0.35) in Arm B (p = .048). The estimated 3-year overall survival rate was 86.4% (±4.4%) and 79.9% (±4.7%) in 2 arms, respectively (p = .155). EFS at 3 years was 79.2% (±4.9%) in Arm A and 60.0% (±5.9%) in Arm B (p = .007). Intracellular reactive oxygen species (ROS) level was found to be reversely correlated with platelet recovery, and fewer patients in Arm A displayed excessive ROS within hematopoietic progenitor cells compared to Arm B. In conclusion, the addition of decitabine and NAC to mBUCY is a feasible and promising conditioning therapy for myeloid malignancies patients.
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