Disminución de mortalidad en hemopatías malignas con un nuevo método de acondicionamiento para trasplante alogénico mieloablativo

IF 0.1 Q4 ONCOLOGY
Eucario León Rodríguez, Mónica M. Rivera Franco
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引用次数: 1

Abstract

Introduction

Allogeneic stem cell transplantation (ASCT) is the ideal treatment for haematological malignancies. However, the morbidity and mortality associated with the procedure limit its use.

Objectives

To describe clinical characteristics, toxicity, and survival of adult Mexican patients undergoing ASCT using busulfan with a reduced dose of cyclophosphamide (BUCY 2) as a conditioning method.

Methods

A prospective cohort study was conducted from October 1999 to December 2014, by performing an analysis of clinical characteristics, complications, and survival of 35 patients using this conditioning regimen.

Results

The study included 35 patients undergoing ASCT with reduced BUCY 2. All of them had an HLA-matched related donor, with a median age of 33 years (range 16-49), and 60% were male. The patients had the following underlying diseases: myelodysplastic syndrome in 14 patients (40%), chronic myeloid leukaemia in 9 (25.7%), acute leukaemia in 10 (23.5%), and paroxysmal nocturnal haemoglobinuria in 2 (5.7%). The median of transfused CD34 + cells was 2.04 × 106/kg. The median time to neutrophil and platelet recovery was 21 and 18 days, respectively. The most common toxicity was mucositis (91.4%). Transplant related mortality was 5.7%, and 5-year overall survival was 72.5%.

Conclusions

The conditioning method described earlier preserves a cytotoxic effect allowing eradication of the malignant clone, and achieving a graft with acceptable toxicity, and low transplant related mortality, representing a good alternative for ASCT.

异体骨髓消融移植新调理方法降低恶性血液病死亡率
同种异体干细胞移植(ASCT)是治疗血液系统恶性肿瘤的理想方法。然而,与手术相关的发病率和死亡率限制了它的使用。目的描述使用布苏凡和减少剂量环磷酰胺(BUCY 2)作为调节方法进行ASCT的墨西哥成年患者的临床特征、毒性和生存率。方法从1999年10月至2014年12月进行前瞻性队列研究,分析35例使用该调理方案的患者的临床特征、并发症和生存率。结果本研究纳入了35例bucy2降低的ASCT患者。所有患者均有hla匹配的亲属供体,中位年龄33岁(16-49岁),60%为男性。患者有以下基础疾病:骨髓增生异常综合征14例(40%),慢性髓性白血病9例(25.7%),急性白血病10例(23.5%),阵发性夜间血红蛋白尿2例(5.7%)。输注CD34 +细胞的中位数为2.04 × 106/kg。中性粒细胞和血小板恢复的中位时间分别为21天和18天。最常见的毒性是粘膜炎(91.4%)。移植相关死亡率为5.7%,5年总生存率为72.5%。结论先前描述的调节方法保留了细胞毒性作用,可以根除恶性克隆,并获得具有可接受毒性的移植物,移植相关死亡率低,是ASCT的良好替代方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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