Vickers Andrew J
Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
J Soc Integr Oncol. 2006 Winter;4(1):46-51.
Phase I trials are an important part of traditional drug development in oncology. Such trials address two key issues: safety and dose. Currently, there is a dearth of phase I trials of anticancer botanicals. This may result from the apparently widespread view that a history of human use precludes the need for early-phase study. However, the safe use of a botanical by the population at large does not guarantee safety when the botanical is used in combination with other agents in the complex medical setting of oncology. Several cases of unpredictable adverse events have been recorded following the use of botanicals by cancer patients. We propose a simple, robust design for phase I trials of anticancer botanicals. This design incorporates important characteristics of botanical medicines including low toxicity, prior data on a likely safe dose, a limit on the highest dose it is feasible to administer, and the unknown relationship between dose-toxicity and dose-response curves. Two principal design features are the use of predetermined dose levels and the direct measurement of a response endpoint such as survival or immunity. This response end point can be used to determine the optimal dose if toxicity is acceptable at all dose levels. Increasing the use of phase I methodology would ensure a more systematic development of botanicals as anticancer agents. This would likely increase the chance that at least one such agent would be proven to extend lives.
I期试验是肿瘤学传统药物研发的重要组成部分。此类试验解决两个关键问题:安全性和剂量。目前,抗癌植物药的I期试验较为匮乏。这可能源于一种普遍的观点,即人类使用历史使得早期研究不再必要。然而,在肿瘤学复杂的医疗环境中,当植物药与其他药物联合使用时,普通人群对植物药的安全使用并不能保证其安全性。癌症患者使用植物药后,已有数例不可预测的不良事件记录。我们提出一种简单、稳健的抗癌植物药I期试验设计。该设计纳入了植物药的重要特性,包括低毒性、可能的安全剂量的先前数据、可行的最高剂量限制以及剂量-毒性和剂量-反应曲线之间的未知关系。两个主要设计特点是使用预定剂量水平和直接测量生存或免疫等反应终点。如果所有剂量水平的毒性均可接受,则该反应终点可用于确定最佳剂量。增加I期方法的使用将确保植物药作为抗癌药物的研发更加系统。这可能会增加至少一种此类药物被证明可延长生命的机会。