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非清髓性异基因造血干细胞移植

Nonmyeloablative allogeneic hematopoietic stem cell transplantation.

作者信息

Baron F, Beguin Y

机构信息

Department of Medicine, Division of Hematology, University of Liège, 4000 Liège, Belgium.

出版信息

J Hematother Stem Cell Res. 2002 Apr;11(2):243-63. doi: 10.1089/152581602753658448.

DOI:10.1089/152581602753658448
PMID:11983097
Abstract

Allogeneic hematopoietic stem cell transplantation (HSCT) is the most effective treatment for selected hematological malignancies. Its curative potential is largely mediated by an immune-mediated destruction of malignant cells by donor lymphocytes termed graft-versus-leukemia (GVL) effect. However, because of its toxicity, conventional allogeneic HSCT is restricted to younger and fitter patients. These observations led several groups to set up new (less toxic) transplant protocols (nonmyeloablative stem cell transplantation or NMSCT) based on a two-step approach: first, the use of immunosuppressive (but nonmyeloablative) preparative regimens providing sufficient immunosuppression to achieve engraftment of allogeneic hematopoietic stem cells and, in a second step, destruction of malignant cells by the GVL effect. Preliminary results showed that NMSCT were feasible with a relatively low transplant-related mortality (TRM), even in patients older than 65 years. In addition, strong antitumor responses were observed in several hematological malignancies as well as in some patients with renal cell carcinoma. After discussing the mechanisms and efficacy of the GVL effect as well as the rationale for NMSCT strategies, this article reviews the first results of ongoing clinical trials. Innovative modalities that may permit amplification of the GVL effect while minimizing the risk of GVHD are discussed. Because the benefits of NMSCT over alternative forms of treatment remain to be demonstrated, this strategy should be restricted to patients included in clinical trials.

摘要

异基因造血干细胞移植(HSCT)是治疗特定血液系统恶性肿瘤最有效的方法。其治愈潜力很大程度上是由供体淋巴细胞介导的对恶性细胞的免疫介导破坏,即移植物抗白血病(GVL)效应。然而,由于其毒性,传统的异基因HSCT仅限于年轻且身体状况较好的患者。这些观察结果促使多个研究小组基于两步法建立了新的(毒性较小的)移植方案(非清髓性干细胞移植或NMSCT):首先,使用免疫抑制(但非清髓性)预处理方案,提供足够的免疫抑制以实现异基因造血干细胞的植入,第二步,通过GVL效应破坏恶性细胞。初步结果表明,即使在65岁以上的患者中,NMSCT也是可行的,移植相关死亡率(TRM)相对较低。此外,在几种血液系统恶性肿瘤以及一些肾细胞癌患者中观察到了强烈的抗肿瘤反应。在讨论了GVL效应的机制和疗效以及NMSCT策略的基本原理后,本文回顾了正在进行的临床试验的初步结果。还讨论了可能在扩大GVL效应的同时将移植物抗宿主病(GVHD)风险降至最低的创新模式。由于NMSCT相对于其他治疗形式的益处仍有待证明,因此该策略应仅限于纳入临床试验的患者。

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Nonmyeloablative allogeneic hematopoietic stem cell transplantation.非清髓性异基因造血干细胞移植
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