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慢性淋巴细胞白血病的口服氟达拉滨疗法——便利性增加。

Oral fludarabine therapy in chronic lymphocytic leukemia--increased convenience.

作者信息

Boogaerts Marc A

机构信息

Department Hematology, University Hospital, Leuven, Belgium.

出版信息

Hematol J. 2004;5 Suppl 1:S31-7. doi: 10.1038/sj.thj.6200389.

DOI:10.1038/sj.thj.6200389
PMID:15079151
Abstract

Intravenous fludarabine is a well-established therapy for the first-line treatment of chronic lymphocytic leukemia and the standard of care for second-line treatment. More recently, an oral formulation of fludarabine has been developed, with equivalent efficacy and tolerability to the intravenous formulation, but with improved convenience of administration and potentially greater cost effectiveness. In previously treated patients receiving oral fludarabine monotherapy, overall response rates of 46-51% were achieved, depending on the response criteria used. Oral fludarabine is also an effective first-line treatment, both as monotherapy (overall response 72-80%) and in combination with cyclophosphamide (overall response 80%). Infusion-related adverse effects are eliminated with oral administration. Importantly, WHO performance status is maintained or improved in more than 50% of patients. As oral fludarabine can be taken at home, administration costs are greatly reduced due to fewer physician and nursing interventions and less time spent in hospital. Oral fludarabine was approved first in the UK as second-line therapy for chronic lymphocytic leukemia and, based on its ease of administration and potentially greater cost effectiveness, is recommended in preference to the intravenous formulation by the UK National Institute for Clinical Excellence. The oral formulation is also now available in the majority of European countries. Therefore, with equivalent efficacy and tolerability to the intravenous preparation, oral fludarabine gives the hematologist an important new option in the management of chronic lymphocytic leukemia.

摘要

静脉注射氟达拉滨是慢性淋巴细胞白血病一线治疗的成熟疗法,也是二线治疗的标准护理方案。最近,已开发出口服氟达拉滨制剂,其疗效和耐受性与静脉制剂相当,但给药便利性有所提高,潜在成本效益更高。在接受口服氟达拉滨单药治疗的既往治疗患者中,根据所使用的反应标准,总体缓解率达到46%-51%。口服氟达拉滨作为单药治疗(总体缓解率72%-80%)或与环磷酰胺联合使用(总体缓解率80%)时,也是一种有效的一线治疗方法。口服给药可消除与输液相关的不良反应。重要的是,超过50%的患者维持或改善了世界卫生组织的体能状态。由于口服氟达拉滨可以在家中服用,减少了医生和护理干预,缩短了住院时间,给药成本大幅降低。口服氟达拉滨最初在英国被批准作为慢性淋巴细胞白血病的二线治疗药物,基于其给药便利性和潜在更高的成本效益,英国国家临床优化研究所建议优先于静脉制剂使用。现在大多数欧洲国家也有口服制剂。因此,口服氟达拉滨与静脉制剂疗效和耐受性相当,为血液科医生在慢性淋巴细胞白血病管理方面提供了一个重要的新选择。

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