非清髓性异基因干细胞移植治疗伊马替尼时代的慢性骨髓性白血病

Richard Champlin, Marcos de Lima, Partow Kebriaei, Gabriela Rondon, Tobi Fisher, Elias Jabbour, Jorge E. Cortés, Hagop Kantarjian, Paolo Anderlini, Amin Alousi, Chitra Hosing, Elizabeth Shpall, Uday Popat, Muzaffar Qazilbash, Borje Andersson, Sergio Giralt
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引用次数: 15

摘要

同种异体干细胞移植(ASCT)是慢性髓性白血病(CML)患者的一种潜在治愈治疗方法,以前被认为是新诊断的CML的首选治疗方法。伊马替尼的成功改变了治疗建议,同种异体移植现在保留给伊马替尼治疗失败的患者。先前的伊马替尼治疗不会影响ASCT的结果,但明显转化疾病的患者效果较差。目前尚不清楚伊马替尼治疗失败的患者是否应立即转诊进行ASCT或接受第二代酪氨酸激酶抑制剂(TKI)治疗。2次tki失败的患者应尽可能接受ASCT。非清髓性预备方案降低了与移植程序相关的毒性和治疗相关死亡率,并允许在老年和身体虚弱的患者中进行移植。这种方法,包括移植后TKIs治疗和供体淋巴细胞输注,产生了很大一部分持久的分子完全缓解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nonmyeloablative Allogeneic Stem Cell Transplantation for Chronic Myelogenous Leukemia in the Imatinib Era

Allogeneic stem cell transplantation (ASCT) is a potentially curative treatment for patients with chronic myelogenous leukemia (CML) and was previously considered the preferred treatment for newly diagnosed CML. The success of imatinib has changed treatment recommendations, and allogeneic transplants are now reserved for imatinib treatment failures. Previous imatinib treatment does not compromise the results of ASCT, but patients with overt transformed disease have poor results. It is unclear whether patients whose disease is considered to have failed imatinib should be referred immediately for ASCT or receive treatment with a second-generation tyrosine kinase inhibitors (TKI). Patients whose disease fails 2 TKIs should receive ASCT if possible. Nonmyeloablative preparative regimens reduce the toxicity and treatment-related mortality associated with the transplantation procedure and allow transplantations to be performed in older and medically infirm patients. This approach, including posttransplantation treatment with TKIs and donor lymphocyte infusion, produces a high fraction of durable molecular complete remissions.

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