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成人高危急性白血病完全单倍体造血干细胞移植的调查:移植时处于缓解期患者结局的危险因素分析

A survey of fully haploidentical hematopoietic stem cell transplantation in adults with high-risk acute leukemia: a risk factor analysis of outcomes for patients in remission at transplantation.

作者信息

Ciceri Fabio, Labopin Myriam, Aversa Franco, Rowe Jakob M, Bunjes Donald, Lewalle Philippe, Nagler Arnon, Di Bartolomeo Paolo, Lacerda João F, Lupo Stanghellini Maria Teresa, Polge Emmanuelle, Frassoni Francesco, Martelli Massimo F, Rocha Vanderson

机构信息

Hematology and BMT Unit, San Raffaele Scientific Institute, Milano, Italy.

出版信息

Blood. 2008 Nov 1;112(9):3574-81. doi: 10.1182/blood-2008-02-140095. Epub 2008 Jul 7.

Abstract

Haploidentical hematopoietic stem cell transplantation (haplo-HSCT) is an alternative treatment to patients with high-risk acute leukemia lacking a human leukocyte antigen-matched donor. We analyzed 173 adults with acute myeloid leukemia (AML) and 93 with acute lymphoblastic leukemia (ALL) who received a haplo-HSCT in Europe. All grafts were T cell-depleted peripheral blood progenitor cells from a direct family or other related donor. At transplantation, there were 25 patients with AML in CR1 (complete remission 1), 61 in more than or equal to CR2, and 87 in nonremission, and 24 with ALL in CR1, 37 in more than or equal to CR2, and 32 in nonremission. Median follow-up was 47 months in AML and 29 months in the ALL groups. Engraftment was observed in 91% of the patients. Leukemia-free survival at 2 years was 48% plus or minus 10%, 21% plus or minus 5%, and 1% for patients with AML undergoing transplantation in CR1, more than or equal to CR2, and nonremission, and 13% plus or minus 7%, 30% plus or minus 8%, and 7% plus or minus 5% in ALL patients, respectively. In conclusion, haplo-HSCT can be an alternative option for the treatment of high-risk acute leukemia patients in remission, lacking a human leukocyte antigen-matched donor.

摘要

单倍体相合造血干细胞移植(haplo-HSCT)是一种针对缺乏人类白细胞抗原匹配供体的高危急性白血病患者的替代治疗方法。我们分析了173例接受单倍体相合造血干细胞移植的欧洲成年急性髓系白血病(AML)患者和93例急性淋巴细胞白血病(ALL)患者。所有移植物均为来自直系亲属或其他相关供体的T细胞去除外周血祖细胞。移植时,AML患者中有25例处于完全缓解1期(CR1),61例处于CR2及以上,87例未缓解;ALL患者中有24例处于CR1,37例处于CR2及以上,32例未缓解。AML组的中位随访时间为47个月,ALL组为29个月。91%的患者实现了造血重建。AML患者在CR1、CR2及以上和未缓解状态下接受移植时,2年无白血病生存率分别为48%±10%、21%±5%和1%;ALL患者的相应生存率分别为13%±7%、30%±8%和7%±5%。总之,对于处于缓解期、缺乏人类白细胞抗原匹配供体的高危急性白血病患者,单倍体相合造血干细胞移植可以作为一种替代选择。

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