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2-氯脱氧腺苷治疗华氏巨球蛋白血症——自身经验分析及文献综述

2-Chlorodeoxyadenosine treatment of Waldenström's macroglobulinemia--the analysis of own experience and the review of literature.

作者信息

Lewandowski K, Zaucha J M, Bieniaszewska M, Hałaburda K, Hellmann A

机构信息

Department of Hematology, Medical University, ul. Debinki 7, 80-211 Gdańsk, Poland.

出版信息

Med Sci Monit. 2000 Jul-Aug;6(4):740-5.

Abstract

INTRODUCTION

The aim of the study was to evaluate the results of treatment of Waldenström's Macroglobulinemia with 2-chlorodeoxyadenosine. The evaluation was based on our own experience as well as on the data published previously in the literature.

MATERIAL AND METHODS

25 patients with Waldenström's Macroglobulinemia (MW) were treated with 2-chlorodeoxyadenosine (2-CdA) at the dose of 0.14 mg/kg b.w./day for five consecutive days as 2-hour intravenous infusions. Chemotherapy was repeated every 28 to 35 days.

RESULTS

In one case (4%) a complete remission and in 15 patients (60%) a partial remission was achieved. In 6 patients (24%) stabilization of the disease was observed while in 3 patients (12%) progression was noted during the treatment. As a result of the therapy, the mean monoclonal protein concentration decreased from 28.7 g/l (range 5.5-62.5 g/l) to 16.7 g/l (range 0-62.9 g/l) and the mean hemoglobin concentration increased from 10.6 g/dl (range 6.9-13.4) to 12.4 g/dl (range 8.2-14.8 g/dl).

CONCLUSION

Our own experience, as well as conclusions of other authors, confirm the effectiveness of 2-CdA in MW treatment. Both the results of treatment and intensity of side effects observed in our treatment group were comparable to those described in previous reports.

摘要

引言

本研究的目的是评估2-氯脱氧腺苷治疗华氏巨球蛋白血症的效果。评估基于我们自己的经验以及先前文献中发表的数据。

材料与方法

25例华氏巨球蛋白血症(MW)患者接受2-氯脱氧腺苷(2-CdA)治疗,剂量为0.14mg/kg体重/天,连续5天,静脉输注2小时。化疗每28至35天重复一次。

结果

1例(4%)完全缓解,15例(60%)部分缓解。6例(24%)疾病稳定,3例(12%)在治疗期间病情进展。治疗后,单克隆蛋白平均浓度从28.7g/l(范围5.5-62.5g/l)降至16.7g/l(范围0-62.9g/l),平均血红蛋白浓度从10.6g/dl(范围6.9-13.4)升至12.4g/dl(范围8.2-14.8g/dl)。

结论

我们自己的经验以及其他作者的结论证实了2-CdA在MW治疗中的有效性。我们治疗组观察到的治疗结果和副作用强度与先前报告中描述的相当。

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