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接受基于地塞米松的非骨髓抑制诱导治疗的多发性骨髓瘤患者自体干细胞移植的结果

Outcomes of autologous stem cell transplantation in patients with multiple myeloma who received dexamethasone-based nonmyelosuppressive induction therapy.

作者信息

Anagnostopoulos A, Aleman A, Yang Y, Donato M, Weber D, Champlin R, Smith T, Alexanian R, Giralt S

机构信息

Department of Blood and Marrow Transplantation, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Bone Marrow Transplant. 2004 Mar;33(6):623-8. doi: 10.1038/sj.bmt.1704398.

Abstract

High-dose chemotherapy (HDC) followed by autologous stem cell transplantation (ASCT) improves survival in myeloma (MM). The role of induction therapy on outcomes of ASCT in MM has not been systematically studied. Nonmyelosuppressive (NMS) steroid-based induction can be used in MM, with the potential of reducing neutropenias and other toxic effects prior to ASCT. NMS induction however could be associated with poorer outcomes if disease control or stem cell collection were inadequate. We studied outcomes of 136 MM patients who underwent HDC and ASCT as part of their initial therapy between March 1998 and December 2000. Of these, 46 received HDC and ASCT without any exposure to myelosuppressive agents, 39 received myelosuppressive therapy for disease control and/or stem cell collection, and 51 received alkylating agent-based initial treatment. We compared OS and EFS rates, stem cell collectability, and contamination of the grafts with monoclonal plasma cells. After a median of 33 months, response rates, EFS and OS rates were comparable in the three groups of patients. Adequacy of stem cell collection and plasma cell contamination were similar. Our data support the hypothesis that NMS induction for patients with MM is safe and effective and does not compromise the results of HDC.

摘要

大剂量化疗(HDC)后进行自体干细胞移植(ASCT)可提高骨髓瘤(MM)患者的生存率。诱导治疗对MM患者ASCT疗效的作用尚未得到系统研究。基于非骨髓抑制(NMS)类固醇的诱导治疗可用于MM患者,有可能减少ASCT前的中性粒细胞减少及其他毒性作用。然而,如果疾病控制或干细胞采集不充分,NMS诱导治疗可能与较差的预后相关。我们研究了1998年3月至2000年12月期间136例接受HDC和ASCT作为初始治疗一部分的MM患者的预后。其中,46例接受HDC和ASCT且未接触任何骨髓抑制药物,39例接受骨髓抑制治疗以控制疾病和/或采集干细胞,51例接受基于烷化剂的初始治疗。我们比较了总生存期(OS)和无事件生存期(EFS)率、干细胞采集能力以及移植物中克隆性浆细胞的污染情况。中位随访33个月后,三组患者的缓解率、EFS和OS率相当。干细胞采集的充分性和浆细胞污染情况相似。我们的数据支持以下假设:MM患者的NMS诱导治疗安全有效,且不会影响HDC的治疗结果。

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