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克拉屈滨的新旧制剂。血液系统恶性肿瘤中的药理学及临床疗效

Older and new formulations of cladribine. Pharmacology and clinical efficacy in hematological malignancies.

作者信息

Robak Tadeusz, Korycka Anna, Robak Ewa

机构信息

Department of Hematology, Medical University of Lodz and Copernicus Memorial Hospital, 93-513 Lodz, Pabianicka 62, Poland.

出版信息

Recent Pat Anticancer Drug Discov. 2006 Jan;1(1):23-38. doi: 10.2174/157489206775246467.

Abstract

The purine nucleoside analog (PNA)--cladribine (2-CdA, 2-chlorodeoxyadenosine) is a cytotoxic agent of high efficacy in lymphoid and myeloid malignancies. This drug was approved by the FDA for treatment of hairy cell leukemia and in some European countries for treatment of refractory/relapsed chronic lymphocytic leukemia. 2-CdA is usually administered as continuous or intermittent intravenous infusion. Recently however, new formulations of this agent has been developed for subcutaneous and oral administration. In contrast to other PNA, 2-CdA is equally cytotoxic to both proliferating and quiescent cells and several pathways may be responsible for the mechanism of its action. In addition, recent data indicate that 2-CdA combined with other cytotoxic agents and monoclonal antibodies show synergistic proapoptotic and cytotoxic activity on lymphoid and myeloid neoplastic cells. This review article summarizes recent achievements in the understanding of 2-CdA mechanism of action, pharmacokinetics of different pharmaceutical formulations and its approved and possible future applications in the treatment of hematological malignancies. The most important recent patents concerning oral formulations of 2-CdA have been presented.

摘要

嘌呤核苷类似物(PNA)——克拉屈滨(2-CdA,2-氯脱氧腺苷)是一种对淋巴和髓系恶性肿瘤具有高效的细胞毒性药物。该药物已获美国食品药品监督管理局(FDA)批准用于治疗毛细胞白血病,在一些欧洲国家也被批准用于治疗难治性/复发性慢性淋巴细胞白血病。2-CdA通常通过持续或间歇静脉输注给药。然而,最近已开发出该药物的新剂型用于皮下和口服给药。与其他PNA不同,2-CdA对增殖细胞和静止细胞具有同等的细胞毒性,其作用机制可能涉及多种途径。此外,最近的数据表明,2-CdA与其他细胞毒性药物和单克隆抗体联合使用时,对淋巴和髓系肿瘤细胞具有协同促凋亡和细胞毒性活性。本文综述了在理解2-CdA作用机制、不同药物剂型的药代动力学及其在血液系统恶性肿瘤治疗中的已批准和可能的未来应用方面的最新进展。还介绍了有关2-CdA口服制剂的最重要的近期专利。

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