Department of Rheumatology and Clinical Immunology, Charité - University Medicine Berlin, Germany.
Curr Opin Rheumatol. 2010 May;22(3):237-45. doi: 10.1097/BOR.0b013e328337b832.
The list of therapeutic targets for the treatment of rheumatic diseases constantly grows. As a consequence, a growing number of agents that are specifically directed against these targets become clinically available. However, the more diverse (and expensive) the armamentarium, the more its use should be guided by informed decisions for an optimal treatment. Such personalized, patient-tailored therapy is still not a reality in rheumatology practice. However, several important steps have recently been made towards achievement of this important goal.
On the basis of the multifactorial nature of the pathogenesis of rheumatic diseases, the quest for single biomarkers that predict treatment response has proven difficult. Instead, biomarker signatures derived from genetic and proteomic expression studies using various biomaterials are being identified and demonstrate predictive value. Research focus has so far been placed on treatment responses to methotrexate and tumor necrosis factor antagonists, but interesting findings are already available for other agents as well.
Although still in their infancy in rheumatology, personalized treatment approaches offer the potential for improved safety and efficacy for the patient and ultimately have promises to reduce societal costs.
治疗风湿性疾病的治疗靶点不断增加。因此,越来越多的针对这些靶点的药物在临床上得到应用。然而,治疗手段(和费用)越多样化,就越应该根据知情决策来指导其使用,以实现最佳治疗效果。这种个性化、针对患者的治疗在风湿病学实践中尚未成为现实。然而,最近在实现这一重要目标方面已经迈出了重要的几步。
基于风湿性疾病发病机制的多因素性质,寻找能够预测治疗反应的单一生物标志物已被证明困难重重。相反,使用各种生物材料进行遗传和蛋白质组表达研究得出的生物标志物特征正在被识别,并显示出预测价值。研究重点一直放在甲氨蝶呤和肿瘤坏死因子拮抗剂的治疗反应上,但其他药物也已经有了有趣的发现。
尽管在风湿病学中仍处于起步阶段,但个性化治疗方法为患者提供了提高安全性和疗效的潜力,并最终有望降低社会成本。