Cho Seongeun, Lau S W Johnny, Tandon Veneeta, Kumi Kofi, Pfuma Elimika, Abernethy Darrell R
Office of Clinical Pharmacology, Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, MD 20993, USA.
Arch Intern Med. 2011 May 23;171(10):937-40. doi: 10.1001/archinternmed.2011.152.
The older population is currently the fastest growing age group in the United States, and this trend is expected to continue for several decades. Older individuals, in general, have a higher disease burden compared with younger adults and are the major users of medications, yet premarketing drug clinical trials have often excluded them even for the drugs that have high utility in this age group. Extrapolation of clinical results from younger to older individuals does not provide adequate benefit-risk estimation, and the frequent need for dose adjustment in older patients from initially approved doses exemplifies the current lack of adequate clinical data in the elderly. Herein, we discuss the information gap for older individuals and the need for a better understanding of the effect of aging on drug responses. We also present cases for future directions, urging the implementation of improved clinical trial designs using new and emerging pharmacokinetic and pharmacodynamic methods to allow the provision of evidence-based individualized treatment to this high drug use group.
老年人群目前是美国增长最快的年龄组,而且这一趋势预计将持续数十年。总体而言,老年人比年轻人有更高的疾病负担,并且是药物的主要使用者,但上市前药物临床试验通常将他们排除在外,即使是对该年龄组有高效用的药物。将年轻个体的临床结果外推至老年人并不能提供充分的效益风险评估,而且老年患者常常需要从最初批准的剂量进行剂量调整,这例证了目前老年人群缺乏充分的临床数据。在此,我们讨论老年人的信息缺口以及更好地理解衰老对药物反应影响的必要性。我们还提出了未来方向的案例,敦促采用新出现的药代动力学和药效学方法实施改进的临床试验设计,以便为这个高药物使用群体提供基于证据的个体化治疗。