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非清髓性干细胞同种异体移植的移植物抗白血病效应可能不足以治愈慢性粒细胞白血病。

The graft-versus-leukemia effect of nonmyeloablative stem cell allografts may not be sufficient to cure chronic myelogenous leukemia.

作者信息

Sloand E, Childs R W, Solomon S, Greene A, Young N S, Barrett A J

机构信息

Stem Cell Allotransplantation Section, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Bone Marrow Transplant. 2003 Nov;32(9):897-901. doi: 10.1038/sj.bmt.1704231.

Abstract

We treated 12 patients with chronic myelogenous leukemia (CML) with a low-intensity preparative regimen followed by allogeneic stem cell transplantation in an attempt to confer a curative graft-versus-leukemia (GVL) effect with minimum morbidity. Seven patients in first chronic phase (CP1) and five in second chronic phase (CP2) (age 15-68 years) received a nonmyeloablative conditioning regimen of fludarabine and cyclophosphamide, followed by a G-CSF-mobilized peripheral blood stem cell (PBSC) transplant from an HLA-identical sibling. Cyclosporine (CsA) was used for graft-versus-host disease (GVHD) prophylaxis. Median follow-up was 384 days. Neutrophil recovery occurred at a median of 12 days. There was no transplant-related mortality. Of the seven CP1 patients transplanted, seven achieved a stable molecular remission; two with no post-transplant intervention, three after donor lymphocytes, imatinib and interferon, and two after a myeloablative stem cell transplant. Four of five CP2 patients died in blast crisis and one survived in molecular remission. Of the 12 patients with durable engraftment, six had Grades II-IV acute GVHD; six had limited chronic GVHD. These results suggest that cytoreduction is required to optimize the curative effect of allogeneic stem cell transplantation for CML.

摘要

我们采用低强度预处理方案,随后进行异基因干细胞移植,治疗了12例慢性粒细胞白血病(CML)患者,试图在最小化发病率的情况下赋予治愈性移植物抗白血病(GVL)效应。7例处于慢性期1(CP1)和5例处于慢性期2(CP2)(年龄15 - 68岁)的患者接受了氟达拉滨和环磷酰胺的非清髓性预处理方案,随后接受来自HLA相合同胞的粒细胞集落刺激因子(G - CSF)动员的外周血干细胞(PBSC)移植。环孢素(CsA)用于预防移植物抗宿主病(GVHD)。中位随访时间为384天。中性粒细胞恢复的中位时间为12天。无移植相关死亡。在接受移植的7例CP1患者中,7例实现了稳定的分子缓解;2例未进行移植后干预,3例在接受供体淋巴细胞、伊马替尼和干扰素治疗后实现缓解,2例在接受清髓性干细胞移植后实现缓解。5例CP2患者中有4例在急变期死亡,1例存活并处于分子缓解状态。在12例实现持久植入的患者中,6例发生了II - IV级急性GVHD;6例发生了局限性慢性GVHD。这些结果表明,需要进行细胞减灭以优化异基因干细胞移植对CML的治愈效果。

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