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[白血病复发的第二次异基因祖细胞移植:10例患者的结果]

[Second allogeneic progenitor cell transplantation for leukemia relapse: results in 10 patients].

作者信息

Martínez C, Carreras E, Sierra J, Rovira M, Urbano-Ispizua A, Viguria M C, Vela D, Rozman C, Montserrat E

机构信息

Escuela de Hematología Farreras-Valentí, Departamento de Medicina, Hospital Clínic i Provincial, Universidad de Barcelona.

出版信息

Med Clin (Barc). 1997 Oct 4;109(11):401-5.

PMID:9379728
Abstract

BACKGROUND

Leukemia relapse is an important cause of treatment failure after allogeneic progenitor cells transplantation. A minority of patients achieve a long-term disease free survival with a second transplant, but the majority die of toxicity or relapse. We report our experience with second allogeneic transplant for leukemia relapse.

PATIENTS AND METHODS

Ten patients were treated with a second transplant. Their diagnosis were chronic myelogenous leukemia (n = 5) and acute leukemia (n = 5). The interval between transplants ranged from 4 to 59 months (median 26 months). Conditioning regimens were busulfan alone (n = 1), associated to cyclophosphamide (n = 6) or to cyclophosphamide plus etoposide (n = 3). Acute graft-versus-host disease (GVHD) prophylaxis consisted of cyclosporin (CSA) (n = 4), CSA plus methotrexate (n = 4), CSA plus prednisolone (n = 1), or CSA, methotrexate plus partial T cell depletion (n = 1).

RESULTS

All patients engrafted after second transplant. Seven developed acute GVHD. Four out of the nine patients at risk (44%) developed chronic GVHD. Three had clinical criteria of hepatic veno-occlusive disease. Three patients died in complete remission due to treatment-related toxicity: pulmonary invasive aspergillosis during an acute GVHD, interstitial pneumonitis plus chronic GVHD, and, hepatic veno-occlusive disease, respectively. Two patients relapsed 4 and 5 months after second transplant. Five remained alive in complete remission after a median follow-up of 27 months. In all of them acute or chronic GVHD incidence and severity after second transplant was higher than after the first transplant. All surviving patients were transplanted more than 12 months after the first transplant.

CONCLUSIONS

A proportion of patients that relapse after an allogeneic progenitor cells transplant may benefit from second transplant; especially, young patients having a good performance status, and with a long interval between transplants.

摘要

背景

白血病复发是异基因祖细胞移植后治疗失败的重要原因。少数患者通过二次移植实现长期无病生存,但大多数患者死于毒性反应或复发。我们报告了我们对白血病复发患者进行二次异基因移植的经验。

患者和方法

10例患者接受了二次移植。他们的诊断为慢性粒细胞白血病(n = 5)和急性白血病(n = 5)。两次移植之间的间隔为4至59个月(中位数26个月)。预处理方案为单用白消安(n = 1)、联合环磷酰胺(n = 6)或联合环磷酰胺加依托泊苷(n = 3)。急性移植物抗宿主病(GVHD)预防方案包括环孢素(CSA)(n = 4)、CSA加甲氨蝶呤(n = 4)、CSA加泼尼松龙(n = 1)或CSA、甲氨蝶呤加部分T细胞清除(n = 1)。

结果

所有患者二次移植后均植入。7例发生急性GVHD。9例有风险的患者中有4例(44%)发生慢性GVHD。3例有肝静脉闭塞病的临床标准。3例患者因治疗相关毒性反应在完全缓解期死亡:分别为急性GVHD期间的肺部侵袭性曲霉病、间质性肺炎加慢性GVHD以及肝静脉闭塞病。2例患者在二次移植后4个月和5个月复发。5例患者在中位随访27个月后仍处于完全缓解状态存活。在所有这些患者中,二次移植后急性或慢性GVHD的发生率和严重程度均高于首次移植后。所有存活患者在首次移植后超过12个月接受移植。

结论

异基因祖细胞移植后复发的一部分患者可能从二次移植中获益;特别是,身体状况良好且两次移植间隔时间长的年轻患者。

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