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甲磺酸伊马替尼用于异基因或同基因造血干细胞移植后复发的费城染色体阳性白血病患者的当前研究结果。

Current results on the use of imatinib mesylate in patients with relapsed Philadelphia chromosome positive leukemia after allogeneic or syngeneic hematopoietic stem cell transplantation.

作者信息

Ullmann Andrew J, Hess Georg, Kolbe Karin, Friedrich-Freksa A, Meyer Ralf G, Gschaidmeier Harald, Huber Christoph, Fischer Thomas

机构信息

3rd Medical Department, Johannes Gutenberg-University, Mainz, Germany.

出版信息

Keio J Med. 2003 Sep;52(3):182-8. doi: 10.2302/kjm.52.182.

Abstract

Here, we describe a patient diagnosed with chronic myelogenous leukemia who relapsed after matched unrelated donor SCT. The patient was treated with imatinib mesylate and donor lymphocyte infusions, and achieved a complete molecular remission. Additionally, safety and efficacy of imatinib mesylate in a total of 134 patients from 8 centers who underwent allogeneic or syngeneic stem cell transplantation (SCT) and had a relapse of Philadelphia chromosome positive leukemia was reviewed. Data was compiled from abstracts accepted as oral or poster presentations at the ASH (American Society of Hematology) 2001 and EBMT (European Group for Blood and Marrow Transplantation) 2001 & 2002 meetings and additionally literature published on this patient group. Efficacy of imatinib therapy was assessed by morphology, cytogenetic analysis, and determination of donor chimerism. In the evaluable population, hematologic and cytogenetic responses were observed in 66% and 60% of the patients, respectively. Fifty-one of 114 (45%) patients achieved a complete cytogenetic response. No response or progress of disease was noted in 22 out of evaluable 91 patients. The observation period was limited to a maximum of 28 months. A significant improvement in donor chimerism was frequently observed. Only five cases of significant GVHD were reported. Preliminary results show that imatinib mesylate has the potential to positively influence the ratio of donor and recipient cells without inducing a high incidence of severe GVHD. The data suggest that earlier start of imatinib mesylate prior to hematologic relapse in minimum residual disease (MRD) positive patients is a promising treatment concept.

摘要

在此,我们描述了一名被诊断为慢性粒细胞白血病的患者,该患者在接受匹配无关供体造血干细胞移植(SCT)后复发。患者接受了甲磺酸伊马替尼和供体淋巴细胞输注治疗,并实现了完全分子缓解。此外,还回顾了甲磺酸伊马替尼在来自8个中心的总共134例接受异基因或同基因干细胞移植(SCT)且费城染色体阳性白血病复发的患者中的安全性和疗效。数据汇编自2001年美国血液学会(ASH)和2001年及2002年欧洲血液和骨髓移植组(EBMT)会议上被接受为口头或壁报展示的摘要,以及另外发表的关于该患者群体的文献。通过形态学、细胞遗传学分析和供体嵌合率测定来评估伊马替尼治疗的疗效。在可评估人群中,分别有66%和60%的患者观察到血液学和细胞遗传学反应。114例患者中有51例(45%)实现了完全细胞遗传学反应。在可评估的91例患者中,有22例未观察到反应或疾病进展。观察期最长为28个月。经常观察到供体嵌合率有显著改善。仅报告了5例严重移植物抗宿主病(GVHD)。初步结果表明,甲磺酸伊马替尼有可能对供体和受体细胞的比例产生积极影响,而不会诱导高发生率的严重GVHD。数据表明,在微小残留病(MRD)阳性患者血液学复发之前更早开始使用甲磺酸伊马替尼是一个有前景的治疗理念。

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