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386例连续性原发性血小板增多症患者的长期随访:血细胞减少治疗的安全性

Long-term follow-up of 386 consecutive patients with essential thrombocythemia: safety of cytoreductive therapy.

作者信息

Palandri Francesca, Catani Lucia, Testoni Nicoletta, Ottaviani Emanuela, Polverelli Nicola, Fiacchini Mauro, De Vivo Antonio, Salmi Federica, Lucchesi Alessandro, Baccarani Michele, Vianelli Nicola

机构信息

Department of Hematology and Medical Oncology L. e A. Seràgnoli, St. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.

出版信息

Am J Hematol. 2009 Apr;84(4):215-20. doi: 10.1002/ajh.21360.

Abstract

Cytotoxic agents like Hydroxyurea, Busulfan and Interferon-alpha are to date the most commonly used therapeutic approaches in Essential Thrombocythemia (ET). However, few data on the efficacy and safety of these agents in the long-term are currently available. We report a retrospective analysis of the long-term outcome of 386 consecutive ET patients, followed at single Institution for a median follow-up of 9.5 years (range, 3-28.5). Cytoreductive therapy was administered to 338 patients (88%), obtaining a response in 86% of cases. Forty-five patients (12%) experienced a thrombosis. Among baseline characteristics, only history of vascular events prior to ET diagnosis predicted a higher incidence of thrombosis. Evolution in acute leukemia/myelofibrosis occurred in 6 (1,5%) and 20 (5%) patients, and was significantly higher in patients receiving sequential cytotoxic agents. Overall survival was 38% at 19 years and was poorer for patients older than 60 years, with higher leukocytes count (>15 x 10(9)/L), hypertension and mellitus diabetes at ET diagnosis and for patients experiencing a thrombotic event during follow-up. Cytoreductive therapy was effective in decreasing platelet number with negligible toxicity; however, thrombocytosis control did not reduce the incidence of thrombosis and, for patients who received sequential therapies, the probability of disease evolution was higher and survival was poorer.

摘要

像羟基脲、白消安和α干扰素这样的细胞毒性药物是目前原发性血小板增多症(ET)中最常用的治疗方法。然而,目前关于这些药物长期疗效和安全性的数据很少。我们报告了对386例连续ET患者长期预后的回顾性分析,这些患者在单一机构接受随访,中位随访时间为9.5年(范围3 - 28.5年)。338例患者(88%)接受了细胞减灭治疗,86%的病例获得了缓解。45例患者(12%)发生了血栓形成。在基线特征中,只有ET诊断前的血管事件史预示着更高的血栓形成发生率。6例(1.5%)和20例(5%)患者发生了急性白血病/骨髓纤维化演变,在接受序贯细胞毒性药物治疗的患者中显著更高。19年时总生存率为38%,60岁以上患者、ET诊断时白细胞计数较高(>15×10⁹/L)、患有高血压和糖尿病的患者以及随访期间发生血栓事件的患者生存率较差。细胞减灭治疗在降低血小板数量方面有效且毒性可忽略不计;然而,血小板增多症的控制并未降低血栓形成的发生率,对于接受序贯治疗的患者,疾病进展的可能性更高且生存率更差。

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