Gilron Ian, Coderre Terence J
Clinical Pain Research, Queen's University, Kingston, Ontario, ON, Canada.
Expert Opin Emerg Drugs. 2007 Mar;12(1):113-26. doi: 10.1517/14728214.12.1.113.
Neuropathic pain is a personally devastating and costly condition affecting 3-8% of the population. Existing treatments have limited effectiveness and produce relatively frequent adverse effects. Preclinical research has identified many promising pharmacological targets; however, reliable predictors of success in humans remain elusive. At least 50 new molecular entities have reached clinical development including: glutamate antagonists, cytokine inhibitors, vanilloid-receptor agonists, catecholamine modulators, ion-channel blockers, anticonvulsants, opioids, cannabinoids, COX inhibitors, acteylcholine modulators, adenosine receptor agonists and several miscellaneous drugs. Eight drugs are in Phase III trials at present. Strategies that may show promise over existing treatments include topical therapies, analgesic combinations and, in future, gene-related therapies. Recent years have heralded an explosion of pharmaceutical development in neuropathic pain, reflecting advanced knowledge of neurobiology and a heightened perception of the commercial value of neuropathic pain therapeutics. In the interest of improving patient care, the authors recommend implementing comparative studies throughout the development process in order to demonstrate the increased value of novel agents.
神经性疼痛是一种对个人具有毁灭性且成本高昂的病症,影响着3%至8%的人口。现有治疗方法效果有限,且相对频繁地产生不良反应。临床前研究已确定了许多有前景的药理学靶点;然而,人类治疗成功的可靠预测指标仍然难以捉摸。至少有50种新的分子实体已进入临床开发阶段,包括:谷氨酸拮抗剂、细胞因子抑制剂、香草酸受体激动剂、儿茶酚胺调节剂、离子通道阻滞剂、抗惊厥药、阿片类药物、大麻素、COX抑制剂、乙酰胆碱调节剂、腺苷受体激动剂以及几种其他药物。目前有8种药物处于III期试验阶段。可能比现有治疗方法更有前景的策略包括局部治疗、镇痛联合用药,以及未来的基因相关治疗。近年来,神经性疼痛的药物开发呈爆发式增长,这反映了神经生物学知识的进步以及对神经性疼痛治疗商业价值的更高认识。为了改善患者护理,作者建议在整个开发过程中开展比较研究,以证明新型药物的更高价值。