American University of Beirut Medical Center, Beirut, Lebanon.
European Society for Blood and Marrow Transplantation Paris Study Office/CEREST-TC, Paris, France.
Clin Lymphoma Myeloma Leuk. 2020 May;20(5):296-304. doi: 10.1016/j.clml.2020.01.007. Epub 2020 Jan 27.
Allogeneic stem cell transplantation is a potentially curative therapy for patients with acute myeloid leukemia (AML) after achieving complete remission (CR). The aim of this study is to evaluate the optimal dose of thiotepa, administered as part of the thiotepa-busulfan-fludarabine (TBF) conditioning regimen for allogeneic stem cell transplantation in adults with AML in CR.
In a retrospective multicenter analysis, we identified 240 patients allotransplanted from matched related or unrelated donors or T replete haplo-identical donors. We compared the transplantation outcomes of patients who received 5 mg/kg thiotepa and 2 days of intravenous busulfan at 6.4 mg/kg (T1B2F) versus those who received 10 mg/kg thiotepa with 2 days of intravenous busulfan at 6.4 mg/kg (T2B2F). The median follow-up was 20 months.
On univariate analysis, the incidence of acute graft versus host disease (GVHD) grade II to IV was significantly lower in the T1B2F group (19%) versus 32% in the T2B2F group (P = .029). This result was confirmed on multivariate analysis; acute GVHD was higher for patients receiving T2B2F (hazard ratio, 2.22; P = .024). No significant change in non-relapse mortality, progression-free survival, or overall survival was observed between the 2 groups.
T2B2F is associated with a higher incidence of acute GVHD compared with T1B2F. These results suggest that a lower dose-intensity of thiotepa and busulfan in the TBF regimen may yield better results in patients with AML in CR.
异体造血干细胞移植是急性髓系白血病(AML)患者在完全缓解(CR)后一种有潜在治愈可能的治疗方法。本研究旨在评估在接受同种异体造血干细胞移植的 CR 期 AML 成人患者中,作为 TBF(噻替哌-白消安-氟达拉滨)预处理方案一部分的噻替哌的最佳剂量。
在回顾性多中心分析中,我们鉴定了 240 例接受来自匹配的亲缘或无关供者或 T 细胞充足的单倍体相合供者的异基因造血干细胞移植的患者。我们比较了接受 5mg/kg 噻替哌和 2 天静脉用 6.4mg/kg 白消安(T1B2F)与接受 10mg/kg 噻替哌和 2 天静脉用 6.4mg/kg 白消安(T2B2F)的患者的移植结果。中位随访时间为 20 个月。
在单变量分析中,T1B2F 组的急性移植物抗宿主病(GVHD)Ⅱ至Ⅳ级的发生率明显低于 T2B2F 组(19%对 32%,P=.029)。这一结果在多变量分析中得到了证实;接受 T2B2F 的患者急性 GVHD 更高(风险比,2.22;P=.024)。两组之间非复发死亡率、无进展生存或总生存均无显著变化。
与 T1B2F 相比,T2B2F 与更高的急性 GVHD 发生率相关。这些结果表明,TBF 方案中噻替哌和白消安的剂量强度降低可能会使 CR 期 AML 患者获得更好的结果。