Dougados Maxime R, van der Heijde Désirée M, Brault Yves, Koenig Andrew S, Logeart Isabelle S
From Paris-Descartes University and the Rheumatology B Department, Cochin Hospital, Paris, France; the Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands; Pfizer France, Paris, France; and Pfizer Inc., Collegeville, Pennsylvania, USA.M.R. Dougados, MD, Professor of Rheumatology, Paris-Descartes University and Rheumatology B Department, Cochin Hospital; D.M. van der Heijde, MD, PhD, Professor of Rheumatology, Leiden University Medical Center; Y. Brault, MS, Director of Biostatistics, Pfizer France; A.S. Koenig, DO, Inflammation and Immunology Group Lead, North America Medical Affairs, Pfizer Inc.; I.S. Logeart, MD, Medical Director, Inflammation Europe, Pfizer France.
J Rheumatol. 2014 Oct;41(10):1922-34. doi: 10.3899/jrheum.131238. Epub 2014 Aug 15.
The objective of these posthoc analyses was to evaluate short-term clinical outcomes as predictors of poor response after 1 year of treatment with combination etanercept/methotrexate (ETN/MTX) therapy versus MTX monotherapy in patients with early rheumatoid arthritis (RA).
Participants with moderate to severe RA [28-joint Disease Activity Score-Erythrocyte Sedimentation Rate (DAS28-ESR) ≥ 3.2] of 3-24 months' duration received ETN 50 mg weekly plus MTX or MTX monotherapy for 52 weeks. Regression analyses were performed to evaluate the likelihood of remission (DAS28-ESR < 2.6) after 1 year despite poor clinical short-term treatment effects (e.g., absolute or changes from baseline in DAS28-ESR after 4, 8, 12, 20, and 24 weeks of therapy).
The magnitude of disease activity and its improvement and timing influenced remission probability in both treatment groups; remission rate was diminished with higher disease activity levels and lower response levels over time from weeks 4 to 24. The rate of DAS28-ESR remission at 1 year was generally greater with ETN/MTX than with MTX alone at most timepoints from weeks 4 to 24. Despite persistent high disease activity (DAS28-ESR > 5.1) after 4, 8, 12, and 24 weeks of therapy, 35%, 27%, 25%, and 22% of patients, respectively, in the ETN/MTX group achieved DAS28-ESR remission after 1 year of continuous treatment; the respective proportions were 33%, 27%, 8%, and 13% in the MTX group.
High disease activity and less improvement with treatment over time in the initial 24 weeks of treatment, particularly after 12 weeks, were predictive of a lower remission rate after 1 year.
这些事后分析的目的是评估在早期类风湿关节炎(RA)患者中,与甲氨蝶呤单药治疗相比,联合使用依那西普/甲氨蝶呤(ETN/MTX)治疗1年后,短期临床结局作为疗效不佳预测指标的情况。
病程为3至24个月的中度至重度RA患者[28个关节疾病活动评分-红细胞沉降率(DAS28-ESR)≥3.2]接受每周50 mg依那西普加甲氨蝶呤或甲氨蝶呤单药治疗52周。进行回归分析以评估尽管短期临床治疗效果不佳(例如,治疗4、8、12、20和24周后DAS28-ESR相对于基线的绝对值或变化),但1年后达到缓解(DAS28-ESR<2.6)的可能性。
两个治疗组中疾病活动的程度及其改善情况和时间均影响缓解概率;从第4周开始到第24周,随着疾病活动水平升高和反应水平降低,缓解率下降。在第4周至第24周的大多数时间点,ETN/MTX组1年时DAS28-ESR缓解率总体上高于甲氨蝶呤单药治疗组。尽管在治疗4、8、12和24周后疾病活动持续处于高水平(DAS28-ESR>5.1),但ETN/MTX组分别有35%、27%、25%和22%的患者在持续治疗1年后实现DAS28-ESR缓解;甲氨蝶呤组的相应比例分别为33%、27%、8%和13%。
在治疗的最初24周,尤其是12周后,疾病活动度高且随着时间推移治疗改善较少,预示着1年后缓解率较低。