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成年治疗相关急性髓系白血病首次缓解期患者的异基因造血细胞移植:与初发急性髓系白血病相当。

Allogeneic hematopoietic cell transplantation for adult patients with treatment-related acute myeloid leukemia during first remission: Comparable to de novo acute myeloid leukemia.

作者信息

Tang Fei-Fei, Huang Xiao-Jun, Zhang Xiao-Hui, Chen Huan, Chen Yu-Hong, Han Wei, Chen Yao, Wang Feng-Rong, Wang Yu, Wang Jing-Zhi, Yan Chen-Hua, Sun Yu-Qian, Mo Xiao-Dong, Liu Kai-Yan, Xu Lan-Ping

机构信息

Peking University People's Hospital, Peking University Institute of Hematology, Beijing, China.

Peking University People's Hospital, Peking University Institute of Hematology, Beijing, China; Peking-Tsinghua Center for Life Sciences, Beijing, China; Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Beijing, China.

出版信息

Leuk Res. 2016 Aug;47:8-15. doi: 10.1016/j.leukres.2016.05.005. Epub 2016 May 12.

DOI:10.1016/j.leukres.2016.05.005
PMID:27239735
Abstract

Therapy-related acute myeloid leukemia (T-AML) is associated with poor prognosis after conventional therapy. Allogeneic hematopoietic cell transplantation (allo-HCT) has been proposed as a treatment for T-AML; however, data comparing outcomes of transplants for patients with de novo AML and T-AML are limited. Sixteen adult patients with T-AML during first complete remission after malignant disease received allo-HCT at the Peking University Institute of Hematology between January 1, 2006 and December 31, 2014. Eighty patients with de novo AML were selected using the case-pair method. The 3-year overall survival and leukemia-free survival for T-AML versus de novo AML patients were 66% vs. 79% (P=0.14) and 64% vs. 77% (P=0.13), respectively. The 3-year cumulative non-relapse mortality rates for T-AML versus de novo AML patients were 13% vs. 9% (P=0.47), respectively; the relapse rates were 20% vs. 13% (P=0.25), respectively. Our results suggest that the prognosis of T-AML is comparable to that of de novo AML after transplantation. Although T-AML shows poorer prognosis than de novo AML after conventional therapies, allo-HCT can markedly improve the prognosis of T-AML.

摘要

治疗相关急性髓系白血病(T-AML)在接受传统治疗后预后较差。异基因造血细胞移植(allo-HCT)已被提议作为T-AML的一种治疗方法;然而,比较初治急性髓系白血病(AML)患者和T-AML患者移植结局的数据有限。2006年1月1日至2014年12月31日期间,16例恶性疾病首次完全缓解期的成年T-AML患者在北京大学生命科学学院接受了allo-HCT。采用病例对照法选取80例初治AML患者。T-AML患者与初治AML患者的3年总生存率和无白血病生存率分别为66%对79%(P=0.14)和64%对77%(P=0.13)。T-AML患者与初治AML患者的3年累积非复发死亡率分别为13%对9%(P=0.47);复发率分别为20%对13%(P=0.25)。我们的结果表明,T-AML移植后的预后与初治AML相当。虽然T-AML在传统治疗后的预后比初治AML差,但allo-HCT可显著改善T-AML的预后。

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