Suppr超能文献

口服氟达拉滨

Oral fludarabine.

作者信息

Plosker Greg L, Figgitt David P

机构信息

Adis International Limited, Auckland, New Zealand.

出版信息

Drugs. 2003;63(21):2317-23. doi: 10.2165/00003495-200363210-00004.

Abstract

Fludarabine is an antimetabolite antineoplastic agent used in the treatment of various haematological malignancies, particularly B-cell chronic lymphocytic leukaemia (CLL). An oral formulation of fludarabine has recently become available in the majority of European countries for the treatment of patients with relapsed or refractory B-cell CLL after initial treatment with an alkylating agent-based regimen. It is the first oral formulation of a purine analogue available for clinical use in B-cell CLL. Pharmacokinetic studies evaluating the bioavailability of oral fludarabine indicate that an oral dose of 40 mg/m2/day would provide similar systemic drug exposure to the standard intravenous dose of 25 mg/m2/day. A phase II study evaluated the clinical efficacy of six to eight cycles of oral fludarabine 40 mg/m2/day for 5 days of each 28-day cycle in 78 patients with previously treated B-cell CLL. Depending on the criteria used, the overall response rate was 46.2% (20.5% complete response [CR], 25.6% partial response [PR]) or 51.3% (17.9% CR, 33.3% PR). These results were similar to the 48% overall response rate reported in a similar historical control group treated with intravenous fludarabine. Myelosuppression (WHO grade 3 or 4) was the most frequently reported adverse effect with oral fludarabine therapy. Other common adverse effects included infection and gastrointestinal disturbances, although these were usually of mild to moderate severity (WHO grade 1 or 2). Overall, the tolerability profile of oral fludarabine is similar to that of the intravenous formulation.

摘要

氟达拉滨是一种抗代谢抗肿瘤药物,用于治疗各种血液系统恶性肿瘤,尤其是B细胞慢性淋巴细胞白血病(CLL)。最近,在大多数欧洲国家,一种口服剂型的氟达拉滨已可用于治疗经基于烷化剂方案初始治疗后复发或难治的B细胞CLL患者。它是首个可用于B细胞CLL临床治疗的嘌呤类似物口服剂型。评估口服氟达拉滨生物利用度的药代动力学研究表明,口服剂量40mg/m²/天可提供与标准静脉剂量25mg/m²/天相似的全身药物暴露。一项II期研究评估了78例先前接受治疗的B细胞CLL患者,在每28天周期的5天内每天口服40mg/m²氟达拉滨,进行6至8个周期治疗的临床疗效。根据所采用的标准,总缓解率为46.2%(完全缓解[CR]为20.5%,部分缓解[PR]为25.6%)或51.3%(CR为17.9%,PR为33.3%)。这些结果与用静脉注射氟达拉滨治疗的类似历史对照组报告的48%总缓解率相似。骨髓抑制(WHO 3级或4级)是口服氟达拉滨治疗最常报告的不良反应。其他常见不良反应包括感染和胃肠道紊乱,不过这些不良反应通常为轻至中度(WHO 1级或2级)。总体而言,口服氟达拉滨的耐受性与静脉剂型相似。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验