Lesko L J, Atkinson A J
Office of Clinical Pharmacology and Biopharmaceutics, Center for Drug Evaluation and Research, Food and Drug Administration, Rockville, Maryland 20852, USA.
Annu Rev Pharmacol Toxicol. 2001;41:347-66. doi: 10.1146/annurev.pharmtox.41.1.347.
In the future, biomarkers will play an increasingly important role in all phases of drug development, including regulatory review. However, only a few of these biomarkers will become established well enough to serve in regulatory decision making as surrogate endpoints, thereby substituting for traditional clinical endpoints. Even generally accepted surrogate endpoints are unlikely to capture all the therapeutic benefits and potential adverse effects a drug will have in a diverse patient population. Accordingly, combinations of biomarkers probably will be needed to provide a more complete characterization of the spectrum of pharmacologic response. In the future, pharmacogenomic approaches, including those based on differential expression of gene arrays, will provide panels of relevant biomarkers that can be expected to transform the drug development process.
未来,生物标志物将在药物研发的各个阶段发挥越来越重要的作用,包括监管审评。然而,这些生物标志物中只有少数能够充分确立,足以作为替代终点用于监管决策,从而替代传统的临床终点。即使是普遍接受的替代终点,也不太可能涵盖药物在不同患者群体中所有的治疗益处和潜在不良反应。因此,可能需要生物标志物组合来更全面地描述药理反应谱。未来,包括基于基因阵列差异表达的方法在内的药物基因组学方法,将提供一系列相关生物标志物,有望改变药物研发过程。