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儿童慢性粒细胞白血病的治疗:甲磺酸伊马替尼(STI-571,格列卫)或异基因造血细胞移植应作为一线治疗方案吗?

Treatment of CML in pediatric patients: should imatinib mesylate (STI-571, Gleevec) or allogeneic hematopoietic cell transplant be front-line therapy?

作者信息

Pulsipher Michael A

机构信息

Blood and Marrow Transplant Program, University of Utah/Primary Children's Medical Center, Salt Lake City, Utah, USA.

出版信息

Pediatr Blood Cancer. 2004 Oct;43(5):523-33. doi: 10.1002/pbc.20062.

Abstract

BACKGROUND

Long-term survival of pediatric patients with chronic myelogenous leukemia (CML) receiving myeloablative hematopoietic stem cell transplantation from fully-matched related and unrelated donors has been reported between 60 and 75%, but is associated with significant morbidity. Imatinib mesylate (STI-571, Gleevec) and reduced intensity conditioning stem cell transplantation (RIC) are two promising new tools that offer potential for decreasing therapy associated morbidity for patients with CML.

RESULTS

Large trials have shown significant responses in chronic phase patients treated with imatinib and reasonable but short-lived responses in advanced phase CML. Data from adult studies is beginning to define populations likely to progress or have prolonged responses to imatinib, and some adult treatment paradigms are moving toward reserving transplantation until patients are at risk of failure with imatinib. Early trials of RIC transplantation in CML show decreased transplant related morbidity with efficacy similar to conventional transplantation, but the approach has yet to be verified in phase III studies. Data in pediatric patients with imatinib and RIC transplantation is limited.

CONCLUSIONS

Studies with imatinib are underway in pediatrics, but whether pediatric dosing schemes will lead to outcomes similar to adults is unknown. Because HLA-matched myeloablative transplantation offers a high rate of cure in the pediatric population, clinical studies assessing the role of imatinib mesylate and RIC transplantation should be planned carefully in order to avoid sub-optimal outcomes.

摘要

背景

据报道,接受来自完全匹配的相关和无关供体的清髓性造血干细胞移植的慢性粒细胞白血病(CML)儿科患者的长期生存率在60%至75%之间,但与显著的发病率相关。甲磺酸伊马替尼(STI-571,格列卫)和减低预处理强度的干细胞移植(RIC)是两种有前景的新方法,它们为降低CML患者治疗相关的发病率提供了可能。

结果

大型试验表明,伊马替尼治疗的慢性期患者有显著反应,而晚期CML患者有合理但短暂的反应。成人研究的数据开始确定可能对伊马替尼病情进展或有长期反应的人群,一些成人治疗模式正朝着保留移植治疗,直到患者有伊马替尼治疗失败风险的方向发展。CML中RIC移植的早期试验显示移植相关发病率降低,疗效与传统移植相似,但该方法尚未在III期研究中得到验证。儿科患者中伊马替尼和RIC移植的数据有限。

结论

儿科正在进行伊马替尼的研究,但儿科给药方案是否会导致与成人相似的结果尚不清楚。由于HLA匹配的清髓性移植在儿科人群中治愈率很高,因此应仔细规划评估甲磺酸伊马替尼和RIC移植作用的临床研究,以避免出现次优结果。

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