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接受氟达拉滨、阿糖胞苷和安吖啶联合治疗后进行减低强度预处理及异基因干细胞移植的难治性急性髓系白血病患者预后的危险因素。

Risk factors for outcome in refractory acute myeloid leukemia patients treated with a combination of fludarabine, cytarabine, and amsacrine followed by a reduced-intensity conditioning and allogeneic stem cell transplantation.

作者信息

Pfrepper Christian, Klink Anne, Behre Gerhard, Schenk Thomas, Franke Georg-Nikolaus, Jentzsch Madlen, Schwind Sebastian, Al-Ali Haifa-Kathrin, Hochhaus Andreas, Niederwieser Dietger, Sayer Herbert Gottfried

机构信息

Abteilung für Hämatologie, Internistische Onkologie, Universitätsklinikum Leipzig, 04103, Leipzig, Germany.

Klinik für Innere Medizin II, Abteilung für Hämatologie und Internistische Onkologie, Universitätsklinikum Jena, Jena, Germany.

出版信息

J Cancer Res Clin Oncol. 2016 Jan;142(1):317-24. doi: 10.1007/s00432-015-2050-y. Epub 2015 Sep 30.

DOI:10.1007/s00432-015-2050-y
PMID:26424692
Abstract

INTRODUCTION

Hematopoietic stem cell transplantation (HCT) is considered a standard treatment for high-risk acute myeloid leukemia (AML) in first or second complete remission (CR). Unfortunately, not all patients achieve complete remission prior to HCT. We sought to establish predictive factors for survival after HCT for refractory AML after FLAMSA-RIC.

PATIENTS AND METHODS

We analyzed the outcome of 44 consecutive patients aged between 21 and 65 years transplanted at the University Hospitals of Jena and Leipzig for refractory AML between 2006 and January 2013. Conditioning for HCT was performed with chemotherapy consisting of fludarabine, cytarabine, and amsacrine followed by total body irradiation or busulfan combined with cyclophosphamide. Antithymocyte globulin was given when transplanting from unrelated donors (FLAMSA-RIC).

RESULTS

Estimated overall survival (OS) and event-free survival (EFS) at 3 years after a median follow-up of 34 (range 6-71) months were 15 and 12 %, respectively. Causes of death were relapse in 66 %, infection in 11 %, and graft-versus-host disease (GvHD) in 7 % of all patients. Twenty-five from 42 evaluable patients (60 %) achieved CR 4 weeks after HCT, while eight patients had partial remission (PR), and nine patients had stable disease (SD). Another six patients with PR and SD achieved CR (overall CR rate 74 %) from 4 weeks to day 90 after HCT following reduction in immunosuppression. The strongest favorable factors in univariate analysis for OS, EFS, and RI were ≥98 % total donor chimerism 2-4 weeks after HCT and <3 lines of pretreatment prior to HCT. In addition, better OS was detected in patients with <20 % bone marrow blasts alone (32 vs. 5 % at 3 years) and in combination with <3 lines of pretreatment (38 vs. 4 % at 3 years). Only a trend for better EFS and lower RI was observed in patients with limited chronic GvHD. In addition, a lower RI was seen in patients with <5 % blasts 4 weeks after HCT. Multivariate analysis revealed that ≥98 % donor chimerism 2-4 weeks after HCT for OS, EFS, and RI and <3 lines of pretreatment for OS and EFS are the strongest predictors for better outcome.

CONCLUSION

FLAMSA-RIC shows long-term survival in refractory AML patients. Factors for favorable outcome are <20 % bone marrow blasts prior to HCT, <3 lines of pretreatment and complete donor chimerism after HCT.

摘要

引言

造血干细胞移植(HCT)被认为是初治或第二次完全缓解(CR)的高危急性髓系白血病(AML)的标准治疗方法。不幸的是,并非所有患者在HCT前都能实现完全缓解。我们试图确定FLAMSA-RIC方案治疗难治性AML后HCT生存的预测因素。

患者与方法

我们分析了2006年至2013年1月期间在耶拿和莱比锡大学医院接受移植的44例年龄在21至65岁之间的难治性AML患者的结局。HCT预处理采用氟达拉滨、阿糖胞苷和安吖啶组成的化疗方案,随后进行全身照射或白消安联合环磷酰胺。从无关供体进行移植(FLAMSA-RIC)时给予抗胸腺细胞球蛋白。

结果

在中位随访34个月(范围6-71个月)后的3年,估计总生存率(OS)和无事件生存率(EFS)分别为15%和12%。所有患者的死亡原因中,66%为复发,11%为感染,7%为移植物抗宿主病(GvHD)。42例可评估患者中有25例(60%)在HCT后4周达到CR,8例患者部分缓解(PR),9例患者疾病稳定(SD)。另外6例PR和SD患者在HCT后4周免疫抑制降低至90天时达到CR(总CR率74%)。单因素分析中,对OS、EFS和复发率(RI)最有利的因素是HCT后2-4周总供体嵌合率≥98%以及HCT前预处理<3线。此外,单独骨髓原始细胞<20%的患者(3年时为32% vs. 5%)以及联合预处理<3线的患者(3年时为38% vs. 4%)的OS更好。慢性GvHD有限的患者仅观察到EFS改善和RI降低的趋势。此外,HCT后4周原始细胞<5%的患者RI较低。多因素分析显示,HCT后2-4周供体嵌合率≥98%对OS、EFS和RI,以及预处理<3线对OS和EFS是更好结局的最强预测因素。

结论

FLAMSA-RIC方案显示难治性AML患者有长期生存。良好结局的因素是HCT前骨髓原始细胞<20%、预处理<3线以及HCT后完全供体嵌合。

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