骨髓增生异常综合征中的自体干细胞移植

Autologous stem cell transplantation in myelodysplastic syndromes.

作者信息

de Witte Theo, Suciu Stefan, Brand Ronald, Muus Petra, Kröger Nicolaus

机构信息

Department of Hematology, Radboud University Medical Centre Nijmegen, Nijmegen, The Netherlands, and Bone Marrow Transplantation, University Hospital Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Semin Hematol. 2007 Oct;44(4):274-7. doi: 10.1053/j.seminhematol.2007.08.006.

Abstract

Allogeneic stem cell transplantation (SCT) is the treatment of choice for the majority of young patients with myelodysplasia (MDS) who have a histocompatible donor (sibling or unrelated donor). For some patients lacking a human leukocyte antigen (HLA)-compatible donor, chemotherapy followed by autologous SCT may be a reasonable alternative, especially for patients with therapy-related MDS/acute myeloid leukemia (AML). A substantial number of candidates may not be eligible for autologous SCT due to failure to induce remission or failure to collect sufficient numbers of stem cells. Careful clinical evaluation of the prognostic factors, such as age, cytogenetic characteristics, chances of achieving complete remission (CR), and availability of a matched unrelated donor, may guide the treating physician in advising the patient about the available treatment options. Mobilized peripheral blood stem cells are the preferred stem cell source for young patients, especially in view of the more rapid hematopoietic recovery after transplantation with mobilized stem cells, but bone marrow stem cells also may be considered for patients older than 50 years. Further development of precise prognostic classification systems, including an accurate evaluation of cytogenetic/molecular response to chemotherapy, is needed to develop a risk-adapted strategy for individual patients.

摘要

对于大多数患有骨髓增生异常综合征(MDS)且有组织相容性供体(同胞或无关供体)的年轻患者而言,异基因干细胞移植(SCT)是首选的治疗方法。对于一些缺乏人类白细胞抗原(HLA)相匹配供体的患者,化疗后进行自体SCT可能是一种合理的替代方案,尤其是对于治疗相关的MDS/急性髓系白血病(AML)患者。由于无法诱导缓解或无法采集到足够数量的干细胞,相当一部分候选患者可能不符合自体SCT的条件。对预后因素进行仔细的临床评估,如年龄、细胞遗传学特征、实现完全缓解(CR)的机会以及匹配的无关供体的可获得性,可能会指导治疗医生就可用的治疗方案向患者提供建议。动员的外周血干细胞是年轻患者首选的干细胞来源,特别是考虑到移植动员干细胞后造血恢复更快,但对于50岁以上的患者也可考虑使用骨髓干细胞。需要进一步开发精确的预后分类系统,包括对化疗的细胞遗传学/分子反应进行准确评估,以制定针对个体患者的风险适应性策略。

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