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供体白细胞输注在异基因干细胞移植后复发性急性白血病治疗中的作用:一项回顾性分析。

The Role of Donor Leukocyte Infusions in the Treatment of Relapsed Acute Leukemia after Allogeneic Stem Cell Transplantation: A Retrospective Analysis.

作者信息

Vaezi Mohammad, Zokaasadi Mohammad, Shahsavari Pour Shervin, Kasaeian Amir, Nikbakht Mohsen, Kamranzadeh Fumani Hosein, Alimoghaddam Kamran, Ghavamzadeh Ardeshir

机构信息

Hematology, Oncology and Stem Cell Transplantation Research Center, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Int J Hematol Oncol Stem Cell Res. 2018 Jul 1;12(3):185-191.

Abstract

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is the only treatment offered for acute leukemias with potential curative capability. One of the main reasons of treatment failure in patients after allo-HSCT is return of the primary disease. This study aimed to evaluate the role of different modalities available to treat the patients with relapsed acute leukemia after allo-HSCT, focusing mainly on donor leukocyte infusions (DLIs). This study included 277 patients who relapsed after myeloablative allo-HSCT between February 2003 and February 2015. Treatment option was offered to all patients, but it was not accepted by about one-third of the study participants. Treated patients were categorized based on receipt of DLI (DLI-based vs. non DLI-based). The effect of treatment in all patients and then the effect of DLI among the treated group was evaluated. Kaplan-Meier method was used for calculating survival rates. All patients were relapsed cases, thus only overall survival (OS) was calculated One hundred and forty-five ALL patients and 132 AML patients were included in the study. One year survival rate for treated patients was 25.13% and for patients who received best supportive care was 2.79% (P<0.001). The difference was significant in both AML and ALL groups. Using DLI-based treatments were accompanied by a noticeably superior outcome. Hazard ratio was 0.43 (0.29-0.63) for DLI-based treatments (P<0.001). Despite the poor prognosis of relapsed acute leukemia after HSCT, it seems that treatment interventions and, especially DLI-based treatments, can be of substantial benefit for patients.

摘要

异基因造血干细胞移植(allo-HSCT)是唯一有望治愈急性白血病的治疗方法。allo-HSCT患者治疗失败的主要原因之一是原发性疾病复发。本研究旨在评估多种治疗方式在allo-HSCT后复发的急性白血病患者中的作用,主要聚焦于供体白细胞输注(DLI)。本研究纳入了2003年2月至2015年2月间接受清髓性allo-HSCT后复发的277例患者。为所有患者提供了治疗方案,但约三分之一的研究参与者未接受。根据是否接受DLI将接受治疗的患者分为两组(基于DLI组与非基于DLI组)。评估了所有患者的治疗效果,以及治疗组中DLI的效果。采用Kaplan-Meier法计算生存率。所有患者均为复发病例,因此仅计算总生存期(OS)。本研究纳入了145例急性淋巴细胞白血病(ALL)患者和132例急性髓细胞白血病(AML)患者。接受治疗患者的一年生存率为25.13%,接受最佳支持治疗患者的一年生存率为2.79%(P<0.001)。AML组和ALL组的差异均具有统计学意义。采用基于DLI的治疗方式的疗效显著更佳。基于DLI的治疗方式的风险比为0.43(0.29 - 0.63)(P<0.001)。尽管HSCT后复发的急性白血病预后较差,但治疗干预措施,尤其是基于DLI的治疗方式,似乎对患者有很大益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f04/6305269/3a9657407a93/IJHOSCR-12-185-g001.jpg

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