Pipobroman therapy of essential thrombocythemia.

M G Mazzucconi, M Francesconi, A Chistolini, E Falcione, A Ferrari, M C Tirindelli, F Mandelli
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引用次数: 35

Abstract

We report our results with pipobroman (PB) therapy in patients with essential thrombocythemia (ET). 21 consecutive untreated patients were treated with PB from 1975 to 1984. PB was given at a dose of 1 mg/kg/d until platelet count dropped below 600 X 10(9)/l. In 18 patients (86%) a hematological remission was obtained. Median duration of induction phase was 49 d. In all cases a maintenance regimen was required at a dose ranging from 0.2 mg/kg/d to 0.5 mg/kg/d, according to platelet number. Follow-up of responder patients ranged from 6 to 108 months (median 17 months). Treatment was well tolerated and we observed only a very moderate and transient hematological toxicity. No patient had relapsed or developed secondary neoplasms at the time of writing. Median survival time of all patients was 24 months (range 10-115).

原发性血小板增多症的Pipobroman治疗。
我们报告了用pipobroman (PB)治疗原发性血小板增多症(ET)患者的结果。从1975年到1984年,连续21例未经治疗的患者接受了PB治疗。以1mg /kg/d的剂量给予PB,直至血小板计数降至600 × 10(9)/l以下。18例患者(86%)获得血液学缓解。诱导期的中位持续时间为49天。在所有病例中,根据血小板数量,维持方案的剂量范围为0.2 mg/kg/d至0.5 mg/kg/d。应答患者的随访时间为6 ~ 108个月(中位17个月)。治疗耐受性良好,我们观察到只有非常中度和短暂的血液毒性。在撰写本文时,没有患者复发或发生继发性肿瘤。所有患者的中位生存时间为24个月(范围10-115)。
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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