Rowinsky E K, Donehower R C
Johns Hopkins Oncology Center, Division of Pharmacology and Experimental Therapeutics, Baltimore, MD 21287-8934.
Semin Oncol. 1993 Aug;20(4 Suppl 3):16-25.
Although paclitaxel (TAXOL) may be one of the most important antineoplastic agents to emerge from drug screening over the last several decades, with activity demonstrated to date against ovarian, breast, lung, and head and neck cancers, there is a relative lack of pharmacologic data available compared with other agents in similar phases of development. This has been due to the aqueous insolubility of paclitaxel and the inherent insensitivity of standard analytic assays in measuring the full range of biologically significant drug concentrations achieved in small animals, a fact that has limited preclinical pharmacologic studies. This report reviews the clinical pharmacology of paclitaxel as determined during early single-agent studies with the drug administered in various intravenous and intraperitoneal schedules and in combination with other antineoplastic agents. Additionally, available information pertaining to the pharmacodynamic and metabolic profiles of paclitaxel is discussed. Such information may be useful in designing rational treatment regimens using paclitaxel as a single agent and in chemotherapy combinations, potentially resulting in the optimal use of this important agent in cancer chemotherapeutics.
尽管紫杉醇(泰素)可能是过去几十年来药物筛选中出现的最重要的抗肿瘤药物之一,目前已证明其对卵巢癌、乳腺癌、肺癌以及头颈癌均有活性,但与处于相似研发阶段的其他药物相比,其可用的药理学数据相对较少。这是由于紫杉醇在水中的不溶性以及标准分析测定法在测量小动物体内达到的所有具有生物学意义的药物浓度时固有的不敏感性,这一事实限制了临床前药理学研究。本报告回顾了紫杉醇的临床药理学,这些药理学是在早期单药研究中确定的,药物以各种静脉内和腹膜内给药方案给药,并与其他抗肿瘤药物联合使用。此外,还讨论了有关紫杉醇药效学和代谢概况的现有信息。此类信息可能有助于设计以紫杉醇作为单药以及化疗联合用药的合理治疗方案,从而有可能在癌症化疗中最佳地使用这一重要药物。