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雄激素治疗血小板减少的骨髓增生异常综合征:20例报告

Androgen therapy in myelodysplastic syndromes with thrombocytopenia: a report on 20 cases.

作者信息

Wattel E, Cambier N, Caulier M T, Sautière D, Bauters F, Fenaux P

机构信息

Service des Maladies du Sang, CHU, Lille, France.

出版信息

Br J Haematol. 1994 May;87(1):205-8. doi: 10.1111/j.1365-2141.1994.tb04895.x.

Abstract

Twenty patients with myelodysplastic syndromes (MDS) and (i) platelets < 50 x 10(9)/l and (ii) bone marrow blasts < or = 10% were treated with androgen therapy (fluoxymesterone at 1 mg/kg/d: seven patients; danazol at 600 mg/d: 13 patients) for at least 3 months. 11 of them (55%) had an increase in platelet counts by at least 30 x 10(9)/l and a disappearance of bleeding symptoms was seen in 6/6 patients with initial bleeding. A response with neutrophil counts (six cases) or haemoglobin levels (five cases) was less often seen. Treatment was continued for 3+ to 27 months in responders (the dose being reduced by 50% after 6 months). Seven patients on maintenance treatment were still responding. Another patient died while he was still responding, and the remaining three patients relapsed after discontinuation (two cases) and dose reduction to 50% (one case) of the androgen used. Side-effects of treatment were moderate. In our experience, androgen therapy can be useful in patients with 'low risks' MDS (i.e. with marrow blasts < or = 10%) and severe thrombocytopenia, especially because no growth factor regularly active on platelets is currently available.

摘要

20例骨髓增生异常综合征(MDS)患者,满足(i)血小板计数<50×10⁹/L且(ii)骨髓原始细胞<或 = 10%,接受雄激素治疗(氟甲睾酮1mg/kg/d:7例患者;达那唑600mg/d:13例患者)至少3个月。其中11例(55%)血小板计数至少增加30×10⁹/L,6例初始有出血症状的患者中出血症状消失。较少见到中性粒细胞计数(6例)或血红蛋白水平(5例)有反应。有反应的患者持续治疗3 +至27个月(6个月后剂量减少50%)。7例维持治疗的患者仍有反应。另1例患者在仍有反应时死亡,其余3例患者在停药(2例)和将雄激素剂量减至50%(1例)后复发。治疗的副作用较轻。根据我们的经验,雄激素治疗对“低危”MDS(即骨髓原始细胞<或 = 10%)且严重血小板减少的患者可能有用,特别是因为目前尚无对血小板有规律活性的生长因子。

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