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异基因骨髓移植治疗成人费城染色体阴性急性淋巴细胞白血病完全缓解后复发的疗效。

Outcome of allogeneic bone marrow transplantation from unrelated donors for adult Philadelphia chromosome-negative acute lymphocytic leukemia in first complete-remission.

机构信息

Department of Hematology, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan.

出版信息

Int J Hematol. 2010 Apr;91(3):419-25. doi: 10.1007/s12185-010-0509-9. Epub 2010 Feb 10.

Abstract

The indication of allogeneic stem cell transplantation (allo-SCT) for Philadelphia chromosome-negative acute lymphocytic leukemia [Ph(-) ALL] from unrelated donors is not established. To assess its potency of unrelated patients in first complete-remission (CR1) transplanted from unrelated donors and the potential prognostic factors affecting the probability of survival, we retrospectively analyzed a total of 41 adult Ph(-) ALL patients in CR1 who underwent unrelated bone marrow transplantation at 6 transplantation centers of the Nagoya Blood and Marrow Transplantation Group between 1993 and 2006. The median age of the 41 patients was 28 years (range, 18-51 years). HLA was matched in 33 transplants, with mismatches in 8 (HLA-A allele mismatch:1, HLA-DR serological mismatch: 2, HLA-DRB1 mismatch: 5). Leukemia-free survival (LFS) at 3 and 6 years from allo-SCT was 60.3 and 47.7%, respectively. LFS at 5 years was 62.1% for those transplanted from HLA-matched donors. LFS was significantly lower with HLA-mismatched donors due to higher transplantation-related mortality. Relapse was observed in 3 patients. Our study suggested that unrelated allo-SCT could improve LFS of patients with a potential graft-versus-leukemia effect. Unrelated allo-SCT for Ph(-) ALL patients in CR1 could be more beneficial by reducing TRM, such as selecting a HLA-matched donor.

摘要

异基因造血干细胞移植(allo-SCT)治疗费城染色体阴性急性淋巴细胞白血病(Ph(-) ALL)患者来自无关供者的适应证尚未确定。为了评估异基因无关供者在首次完全缓解(CR1)期移植的无关患者的疗效以及影响生存概率的潜在预后因素,我们回顾性分析了名古屋血液和骨髓移植组的 6 个移植中心在 1993 年至 2006 年间对 41 例 Ph(-) ALL 成人患者在 CR1 期接受无关骨髓移植的资料。41 例患者的中位年龄为 28 岁(范围 18-51 岁)。在 33 例移植中 HLA 匹配,8 例存在错配(HLA-A 等位基因错配:1 例,HLA-DR 血清学错配:2 例,HLA-DRB1 错配:5 例)。allo-SCT 后 3 年和 6 年的无白血病生存率(LFS)分别为 60.3%和 47.7%。HLA 匹配供者移植的 5 年 LFS 为 62.1%。由于移植相关死亡率较高,HLA 错配供者的 LFS 明显较低。3 例患者出现复发。我们的研究表明,异基因无关造血干细胞移植可改善潜在移植物抗白血病效应的患者的 LFS。通过减少移植相关死亡率(TRM),例如选择 HLA 匹配的供者,异基因无关供者的移植对 CR1 期 Ph(-) ALL 患者可能更有益。

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