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异基因骨髓移植后复发的急性淋巴细胞白血病采用化疗后给予粒细胞集落刺激因子动员的供者白细胞输注治疗的前瞻性研究。

Treatment of relapsed acute lymphoblastic leukemia after allogeneic bone marrow transplantation with chemotherapy followed by G-CSF-primed donor leukocyte infusion: a prospective study.

作者信息

Choi S-J, Lee J-H, Lee J-H, Kim S, Lee Y-S, Seol M, Ryu S-G, Lee J-S, Kim W-K, Jang S, Park C-J, Chi H-S, Lee K-H

机构信息

Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

出版信息

Bone Marrow Transplant. 2005 Jul;36(2):163-9. doi: 10.1038/sj.bmt.1705024.

Abstract

Donor leukocyte infusion (DLI) alone has very limited efficacy for patients with acute lymphoblastic leukemia (ALL) who have relapsed after allogeneic bone marrow transplantation (BMT). We, therefore, prospectively tested the efficacy of cytoreductive chemotherapy (intermediate-dose cytarabine+idarubicin+etoposide) followed immediately by G-CSF-primed DLI (Chemo-DLI) in 10 relapsed ALL patients after allogeneic BMT. Seven achieved complete remission (CR) at a median of 25 days (19-73 days) after DLI. Of these seven CR patients, only one remains alive in CR 907 days after DLI. Two CR patients died in CR of graft-versus-host disease. The remaining four CR patients relapsed at a median of 153 days (120-991 days) after DLI. One is alive with leukemia at post-DLI day 1217. The median survival duration after DLI was 175 days (15-1217 days). In summary, although Chemo-DLI for relapsed ALL after allogeneic BMT induced a relatively high CR rate, durable remissions were rare. Although our data should be interpreted cautiously considering the small number of patients, these results suggest that poor outcome of DLI in relapsed ALL may be primarily due to intrinsic resistance to graft-versus-leukemia effect rather than to the rapid pace of the disease.

摘要

对于异基因骨髓移植(BMT)后复发的急性淋巴细胞白血病(ALL)患者,单纯供体白细胞输注(DLI)的疗效非常有限。因此,我们前瞻性地测试了减瘤化疗(中剂量阿糖胞苷+伊达比星+依托泊苷)后立即进行G-CSF预处理的DLI(化疗-DLI)对10例异基因BMT后复发的ALL患者的疗效。7例在DLI后中位25天(19-73天)达到完全缓解(CR)。在这7例CR患者中,只有1例在DLI后907天仍处于CR状态存活。2例CR患者死于CR期的移植物抗宿主病。其余4例CR患者在DLI后中位153天(120-991天)复发。1例在DLI后第1217天白血病存活。DLI后的中位生存时间为175天(15-1217天)。总之,尽管异基因BMT后复发的ALL患者采用化疗-DLI诱导了相对较高的CR率,但持久缓解很少见。尽管考虑到患者数量较少,我们的数据应谨慎解读,但这些结果表明,复发ALL患者DLI预后不良可能主要是由于对移植物抗白血病效应的内在抵抗,而非疾病进展迅速。

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