StatLog, Inc., Quebec, Canada.
Pfizer Inc., New York, NY, USA.
Curr Med Res Opin. 2021 Dec;37(12):2185-2196. doi: 10.1080/03007995.2021.1981278. Epub 2021 Oct 11.
Long-term real-world management of inflammatory rheumatic diseases remains unclear, especially with the advent of new treatment options. This study characterizes the number of advanced treatments used by patients with selected rheumatic diseases (rheumatoid arthritis [RA], psoriatic arthritis [PsA], ankylosing spondylitis, juvenile idiopathic arthritis) and provides a contemporary portrait of treatment patterns and therapeutic sequencing among patients with RA and PsA.
Patients were selected from a large US claims database and classified into disease subsamples based on the latest rheumatic diagnosis recorded before/on the day of initiation of the first advanced treatment (index date). The total number of advanced treatments was assessed within the first 5 years following the index date. Treatment patterns and therapeutic sequencing were assessed over the first 2 years.
Approximately 20% of patients received ≥2 distinct advanced treatments during the first year following index date - the proportion increased to almost 50% among patients with 5 years of observation. Most patients (RA: 76.8%; PsA: 88.7%) initiated a tumor necrosis factor as the first advanced treatment. Over the first 2 years after the index date, 1/3 of RA and PsA patients switched to another advanced treatment. More than 50% initiated a second treatment with the same mechanism of action (MOA). A small proportion of patients received a biosimilar.
Despite advent of treatments with different MOA, cycling between treatments with the same MOA was common. Further studies with longer data follow-up would be needed to assess the impact of higher adoption of biosimilars on treatment patterns/sequencing.
新的治疗选择出现后,炎症性风湿病的长期真实世界管理仍不明确。本研究旨在描述选定风湿病(类风湿关节炎[RA]、银屑病关节炎[PsA]、强直性脊柱炎、幼年特发性关节炎)患者使用的高级治疗数量,并描绘 RA 和 PsA 患者的治疗模式和治疗顺序的现状。
从大型美国索赔数据库中选择患者,并根据首次高级治疗(索引日期)前/当天记录的最新风湿病诊断将患者分类为疾病亚组。在索引日期后的前 5 年内评估使用高级治疗的总次数。在最初的 2 年内评估治疗模式和治疗顺序。
大约 20%的患者在索引日期后的第一年接受了≥2 种不同的高级治疗,而在观察 5 年的患者中,这一比例增加到近 50%。大多数患者(RA:76.8%;PsA:88.7%)首先使用肿瘤坏死因子作为高级治疗。在索引日期后的前 2 年内,1/3的 RA 和 PsA 患者改用另一种高级治疗。超过 50%的患者以相同的作用机制(MOA)启动第二种治疗。少数患者接受了生物类似药。
尽管出现了不同 MOA 的治疗方法,但仍普遍存在相同 MOA 之间的治疗转换。需要进行更长时间数据随访的进一步研究,以评估更高比例使用生物类似药对治疗模式/顺序的影响。