Comparable Outcome of Allogeneic versus Autologous Hematopoietic Peripheral Blood Stem Cell Transplantation in Acute Myeloid Leukemia Patients with Normal Karyotype and FLT3-ITD Negative

H. Mahmoud, A. El-Haddad, Omar A. Fahmy, M. Samra, Raafat M. Abdelfattah, Y. Elnahass, Hossam A ElAshtoukh, Gamal M. Fathy, Fatma Elrefaey
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引用次数: 4

Abstract

Introduction: Optimal post-remission treatment for acute myeloid leukemia patients with normal karyotype (AMLNK) in first complete remission (CR1) who lacks an HLA identical donor is still not well-defined. Aim of the Work: To compare the outcome of allogeneic versus autologous peripheral blood stem cell transplantation (PBSCT) in adult AML patients regarding toxicities of transplant procedure, transplant-related mortality (TRM), disease free survival (DFS) and overall survival (OS). Patients and Methods: 43 AML patients were included; 34 patients (with a median age 28 years) received myeloablative allogeneic PBSCT from a matched sibling donor while 9 patients (with a median age 36 years) received PBSC autograft. All patients had a normal karyotype (NK), FMS-like tyrosine kinase 3 internal tandem duplication (FLT3 ITD) negative and were in CR1. Results: After a median follow up of 21.5 months (0.3- 46.5), the cumulative 2-year OS and DFS in the allogeneic group were 73.5% and 70.6% respectively, compared to 74.1% and 64.8%, respectively in the autologous group (p=0.690 and 0.768). Increasing number of consolidation cycles (>3) and lower CD34 stem cell dose were associated with lower relapse rates and higher DFS in the autologous group. Conclusion: Preliminary data show a comparable outcome of autologous compared to allogeneic PBSCT in patients with AML-NK and FLT3 ITD negative in CR1. In absence of matched sibling donor, autologous PBSCT may provide an acceptable post remission therapy for patients with low risk molecular profile.
同种异体与自体造血外周血干细胞移植治疗正常核型和FLT3-ITD阴性急性髓系白血病的比较结果
对于首次完全缓解(CR1)的正常核型(AMLNK)急性髓系白血病患者,缺乏HLA相同供体的最佳缓解后治疗仍不明确。研究目的:比较同种异体和自体外周血干细胞移植(PBSCT)在成人AML患者移植手术的毒性、移植相关死亡率(TRM)、无病生存期(DFS)和总生存期(OS)方面的结果。患者与方法:纳入43例AML患者;34例患者(中位年龄28岁)接受了来自匹配的兄弟姐妹供体的清骨髓异基因PBSCT, 9例患者(中位年龄36岁)接受了自体PBSC移植。所有患者核型正常(NK), fms样酪氨酸激酶3内部串联重复(FLT3 ITD)阴性,CR1。结果:中位随访21.5个月(0.3 ~ 46.5),异体组累计2年OS和DFS分别为73.5%和70.6%,自体组分别为74.1%和64.8% (p=0.690和0.768)。在自体组中,增加巩固周期数(>3)和降低CD34干细胞剂量与较低的复发率和较高的DFS相关。结论:初步数据显示,在AML-NK和FLT3患者中,自体PBSCT与异体PBSCT的结果相当。在没有匹配的兄弟姐妹供体的情况下,自体PBSCT可能为低风险分子特征的患者提供一种可接受的缓解后治疗。
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