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对于原发性难治性急性髓系白血病患者,提供异基因造血干细胞移植是否合适?

Is it appropriate to offer allogeneic hematopoietic stem cell transplantation to patients with primary refractory acute myeloid leukemia?

作者信息

Song K W, Lipton J

机构信息

The Leukemia/Bone Marrow Transplantation Program of British Columbia, Vancouver Hospital and Health Sciences Center, British Columbia Cancer Agency, University of British Columbia, Vancouver, British Columbia, Canada.

出版信息

Bone Marrow Transplant. 2005 Aug;36(3):183-91. doi: 10.1038/sj.bmt.1705038.

Abstract

Although continued advances have been made in the treatment of acute myeloid leukemia (AML), approximately 20-30% of patients will never achieve a remission. For these patients with primary refractory AML, the only curative option remains an allogeneic stem cell transplant. Allogeneic transplantation provides the ability to administer myeloablative doses of chemotherapy or chemoradiotherapy, as well as the advantage of a possible graft-versus-leukemia effect. Difficulty in interpreting the literature is due to selection bias, in particular, the varying definitions of primary refractory disease with respect to the morphological criteria and the number of induction regimen required before being defined as being refractory. Regardless, it is a procedure with high treatment-related mortality and risk of relapse. Most studies demonstrate an event-free survival of 10-20% at 5 years. Predictive factors of outcome include blast cell count in the marrow, karyotype, the number of prior regimen, age, performance status and availability of a related donor. These prognostic factors should be considered prior to offering allogeneic transplantation for primary refractory AML. Those patients with many favorable prognostic factors and an HLA-matched related donor available would be the best candidate for the procedure. Those with many poor prognostic factors and only an unrelated donor available may be better served by being offered palliation or being enrolled in investigational studies.

摘要

尽管急性髓系白血病(AML)的治疗不断取得进展,但仍有大约20%-30%的患者无法实现缓解。对于这些原发性难治性AML患者而言,唯一的治愈选择仍然是异基因干细胞移植。异基因移植能够给予清髓剂量的化疗或放化疗,并且具有可能的移植物抗白血病效应。文献解读的困难源于选择偏倚,尤其是原发性难治性疾病在形态学标准以及被定义为难治之前所需诱导方案数量方面的不同定义。尽管如此,这是一种具有高治疗相关死亡率和复发风险的治疗手段。大多数研究表明5年无事件生存率为10%-20%。预后的预测因素包括骨髓原始细胞计数、核型、既往方案数量、年龄、体能状态以及相关供体的可获得性。在为原发性难治性AML提供异基因移植之前,应考虑这些预后因素。那些具有许多有利预后因素且有HLA匹配的相关供体的患者将是该治疗手段的最佳候选者。那些具有许多不良预后因素且仅有不相关供体的患者,或许接受姑息治疗或参加研究性试验会更好。

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