NIHR clinical research facility, Southampton General Hospital, Southampton University Hospitals NHS Trust, Southampton, UK.
Expert Opin Biol Ther. 2024 Oct;24(10):1109-1117. doi: 10.1080/14712598.2024.2404521. Epub 2024 Sep 18.
Rheumatoid arthritis (RA) is a chronic autoimmune inflammatory disease that primarily affects middle-aged individuals but is increasingly prevalent among the elderly due to longer life expectancies. Treating elderly onset RA (EORA) is challenging for clinicians because of unique disease characteristics, comorbidities, polypharmacy, age-related physiological changes, and limited studies on the safety and efficacy of biological therapies in this population. This review aims to evaluate the use of various biological therapies in elderly RA patients.
This narrative review examines various aspects of RA in the elderly using published literature, randomized control trials, meta-analyses, and recommendations from the National Institute for Health and Care Excellence (NICE) and The European Alliance of Associations for Rheumatology (EULAR).
In EORA patients, the initiation of biological therapy is often delayed. Methotrexate remains the first-line treatment for both EORA and young onset RA (YORA). The combination of methotrexate and biological treatment shows comparable safety and efficacy in both EORA and YORA, except for rituximab, which is less effective in patients over 75. For elderly RA patients, biological (b-) disease-modifying antirheumatic drugs (DMARDs) are preferred as the first advanced therapy over targeted synthetic (ts-) DMARDs due to their superior safety profile.
类风湿关节炎(RA)是一种慢性自身免疫性炎症性疾病,主要影响中年人群,但由于预期寿命延长,老年人群中 RA 的发病率也越来越高。由于疾病的独特特征、合并症、多种药物治疗、与年龄相关的生理变化以及针对该人群的生物治疗安全性和疗效的研究有限,治疗老年起病的 RA(EORA)对临床医生来说具有挑战性。本篇综述旨在评估各种生物疗法在老年 RA 患者中的应用。
本叙述性综述使用已发表的文献、随机对照试验、荟萃分析以及英国国家卫生与保健优化研究所(NICE)和欧洲抗风湿病联盟(EULAR)的建议,从多个方面评估了老年 RA 患者的情况。
在 EORA 患者中,生物治疗的起始通常会被延迟。甲氨蝶呤仍然是 EORA 和年轻起病的 RA(YORA)的一线治疗药物。甲氨蝶呤联合生物治疗在 EORA 和 YORA 中显示出相似的安全性和疗效,除了利妥昔单抗,其在 75 岁以上患者中的疗效较差。对于老年 RA 患者,由于生物(b)改善病情的抗风湿药物(DMARDs)具有更好的安全性,因此优先作为一线高级治疗药物,而非靶向合成(ts)DMARDs。