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酪氨酸激酶抑制剂治疗时代异基因 SCT 治疗慢性髓性白血病患者的结局。

Outcome of allogeneic SCT in patients with chronic myeloid leukemia in the era of tyrosine kinase inhibitor therapy.

机构信息

Department for Stem Cell Transplantation, University Cancer Center Hamburg (UCCH), Martinistr. 52, 20246, Hamburg, Germany.

出版信息

Ann Hematol. 2013 Apr;92(4):487-96. doi: 10.1007/s00277-012-1650-8. Epub 2012 Dec 19.

DOI:10.1007/s00277-012-1650-8
PMID:23250623
Abstract

The introduction of tyrosine kinase inhibitors (TKIs) for chronic myeloid leukemia (CML) led to a dramatic change in the role of allogeneic stem cell transplantation (SCT) with a rapid decline in the number of patients receiving SCT in first chronic phase (CP1). We evaluated 68 consecutive patients in all phases of CML (male/female = 39:29, 27 in CP1), who received SCT from related/unrelated donors (related/unrelated = 23:45) under myeloablative or reduced intensity conditioning (MAC/RIC = 45:23). Forty-eight patients (71 %) received TKIs pre-SCT, 20 patients post-SCT (29 %). Overall survival (OS) of CP1 patients achieved a plateau of 85 % at 10 months. Relapse-free survival (RFS) of CP1 patients was 85 % at 1 and 2 years, and 81 % at 5 years. Multivariate analysis showed adverse OS and RFS for patients transplanted >CP1 (hazard ratio (HR) = 6.61 and 4.62) and those who had grade III-IV aGvHD (HR = 2.45 and 1.82). Patients with advanced CML had estimated OS of 65 and 47 %; and RFS of 41 and 32 % at 1 and 2 years respectively. Therefore, for patients with advanced CML phases, allogeneic SCT provides an acceptable chance of cure. Transplant research should focus on improving conditioning regimens and post-SCT management for this subgroup of CML patients.

摘要

酪氨酸激酶抑制剂(TKI)在慢性髓性白血病(CML)中的应用,导致同种异体造血干细胞移植(allo-SCT)的角色发生了重大变化,接受首次慢性期(CP1)allo-SCT 的患者数量迅速减少。我们评估了 68 例 CML 各期(男/女=39:29,CP1 期 27 例)连续患者,他们接受亲缘/非亲缘供者(亲缘/非亲缘=23:45)异基因造血干细胞移植,预处理方案为清髓性或减低强度(MAC/RIC=45:23)。48 例(71%)患者在 allo-SCT 前接受 TKI 治疗,20 例(29%)在 allo-SCT 后接受 TKI 治疗。CP1 患者的总生存(OS)在 10 个月时达到 85%的平台期。CP1 患者的无复发生存(RFS)在 1 年和 2 年时分别为 85%和 81%,在 5 年时为 76%。多变量分析显示,移植>CP1(危险比(HR)=6.61 和 4.62)和发生 III-IV 级移植物抗宿主病(GVHD)(HR=2.45 和 1.82)的患者 OS 和 RFS 不良。晚期 CML 患者的估计 OS 分别为 65%和 47%;1 年和 2 年时的 RFS 分别为 41%和 32%。因此,对于晚期 CML 患者,allo-SCT 提供了可接受的治愈机会。移植研究应集中于改善该组 CML 患者的预处理方案和 allo-SCT 后管理。

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