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接受促红细胞生成素治疗的骨髓增生异常综合征和再生障碍性贫血患者内源性促红细胞生成素水平的系列变化。

Serial changes in endogenous erythropoietin levels in patients with myelodysplastic syndromes and aplastic anemia undergoing erythropoietin treatment.

作者信息

Yoshida Y, Anzai N, Kawabata H, Kohsaka Y, Okuma M

机构信息

Department of Medicine, Faculty of Medicine, Kyoto University, Japan.

出版信息

Ann Hematol. 1993 Apr;66(4):175-80. doi: 10.1007/BF01703232.

DOI:10.1007/BF01703232
PMID:8485205
Abstract

Recombinant human erythropoietin (rhEpo) was administered to 14 patients with myelodysplastic syndrome (MDS) and seven patients with aplastic anemia (AA). In 19 patients, doses of 6000 units were given intravenously three times a week (t.i.w.) with the dose being doubled up to 24,000 units every 8 weeks until a response was obtained. RhEpo was given subcutaneously in two patients. Seven patients, four with MDS and three with AA, showed a significant response with an increase of hemoglobin concentration during therapy. The response occurred at doses of 12,000 units in five and 24,000 units in two patients. Responding patients with both MDS and AA had a relatively low serum Epo (s-Epo) level prior to Epo therapy. MDS responders had either refractory anemia (RA) or RA with ring sideroblasts (RARS), while two of the Epo responders in AA had a severe form of the disease. However, since some of the Epo responders had a high initial s-Epo concentration, a high s-Epo level does not preclude the use of rhEpo. Serial determination of s-Epo levels showed a progressive decline in six of the seven responders even when they were on rhEpo therapy, while the s-Epo levels remained elevated or further increased with time in most nonresponders. RhEpo was well tolerated by all patients. The results suggest that rhEpo is a safe and effective treatment for a certain proportion of patients with MDS and AA. Moreover, serial determination of s-Epo during therapy may be useful in monitoring and predicting the therapeutic effect of rhEpo.

摘要

将重组人促红细胞生成素(rhEpo)应用于14例骨髓增生异常综合征(MDS)患者和7例再生障碍性贫血(AA)患者。19例患者静脉注射剂量为6000单位,每周3次(t.i.w.),每8周剂量加倍至24,000单位,直至获得反应。2例患者皮下注射rhEpo。7例患者,4例MDS患者和3例AA患者,在治疗期间血红蛋白浓度升高,显示出显著反应。5例患者在剂量为12,000单位时出现反应,2例患者在剂量为24,000单位时出现反应。MDS和AA的反应性患者在Epo治疗前血清Epo(s-Epo)水平相对较低。MDS反应者为难治性贫血(RA)或伴有环形铁粒幼细胞的RA(RARS),而AA中的2例Epo反应者患有严重形式的疾病。然而,由于一些Epo反应者初始s-Epo浓度较高,高s-Epo水平并不排除使用rhEpo。连续测定s-Epo水平显示,7例反应者中有6例即使在接受rhEpo治疗时也逐渐下降,而大多数无反应者的s-Epo水平随时间保持升高或进一步升高。所有患者对rhEpo耐受性良好。结果表明,rhEpo对一定比例的MDS和AA患者是一种安全有效的治疗方法。此外,治疗期间连续测定s-Epo可能有助于监测和预测rhEpo的治疗效果。

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Inadequate erythropoietin response to anemia: definition and clinical relevance.对贫血的促红细胞生成素反应不足:定义及临床意义。
Ann Hematol. 1994 May;68(5):215-23. doi: 10.1007/BF01737420.
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Hematopoietic growth factors and the treatment of tumor-associated anemias.造血生长因子与肿瘤相关性贫血的治疗
Ann Hematol. 1994 Nov;69(5):213-21. doi: 10.1007/BF01700275.
3
Controversies in selection of epoetin dosages. Issues and answers.促红细胞生成素剂量选择中的争议。问题与解答。

本文引用的文献

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Serum erythropoietin titers in the anemia of chronic renal failure and other hematological states.慢性肾衰竭贫血及其他血液学状态下的血清促红细胞生成素滴度
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Circulating erythropoietin in patients with myelodysplastic syndromes.骨髓增生异常综合征患者的循环促红细胞生成素
Br J Haematol. 1989 Sep;73(1):36-9. doi: 10.1111/j.1365-2141.1989.tb00215.x.
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Treatment of the anemia of progressive renal failure with recombinant human erythropoietin.用重组人促红细胞生成素治疗进行性肾衰竭贫血。
N Engl J Med. 1989 Jul 20;321(3):158-63. doi: 10.1056/NEJM198907203210305.
10
Radioimmunoassay for erythropoietin using anti-recombinant erythropoietin antibody with high affinity.使用具有高亲和力的抗重组促红细胞生成素抗体的促红细胞生成素放射免疫测定法。
Clin Chim Acta. 1989 Nov;185(2):177-84. doi: 10.1016/0009-8981(89)90040-5.