Tofacitinib Efficacy in Patients with Rheumatoid Arthritis and Probable Depression/Anxiety: Post Hoc Analysis of Phase 3 and 3b/4 Randomized Controlled Trials

被引:2
|
作者
Citera, Gustavo [1 ]
Jain, Rakesh [2 ]
Irazoque, Fedra [3 ]
Madariaga, Hugo [4 ]
Gruben, David [5 ]
Wang, Lisy [5 ]
Stockert, Lori [6 ]
Santana, Karina [7 ]
Ebrahim, Abbas [6 ]
Ponce de Leon, Dario [8 ]
机构
[1] Inst Rehabil Psicofis, Buenos Aires, Argentina
[2] Texas Tech Univ, Sch Med, Midland, TX USA
[3] Hosp Angeles Mocel, San Miguel, Mexico
[4] Clin Sur, Arequipa, Peru
[5] Pfizer Inc, Groton, CT USA
[6] Pfizer Inc, Collegeville, PA USA
[7] Pfizer Inc, Mexico City, Mexico
[8] Pfizer Inc, Orquideas 585, San Isidro 15046, Lima, Peru
关键词
Anxiety; JAK inhibitor; Rheumatoid arthritis; Tofacitinib; PSORIATIC-ARTHRITIS; ANXIETY; METHOTREXATE; ADALIMUMAB; SYMPTOMS; ASSOCIATION; COMBINATION; MONOTHERAPY; CP-690,550; INHIBITORS;
D O I
10.1007/s40744-023-00612-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: The aim of our work is to assess the prevalence of probable major depressive disorder and/or probable generalized anxiety disorder (pMDD/pGAD) in patients with moderate to severe rheumatoid arthritis (RA), and to evaluate the efficacy of tofacitinib on RA symptoms stratified by baseline pMDD/pGAD status.Methods: Data were pooled from five phase 3 randomized controlled trials (RCTs) and one phase 3b/4 RCT, assessing tofacitinib 5 or 10 mg twice daily (BID), adalimumab (two RCTs), or placebo. pMDD/pGAD was defined as Short Form-36 Health Survey (SF-36) Mental Component Summary (MCS) score <= 38. Efficacy outcomes over 12 months included least squares mean change from baseline in SF-36 MCS score and Health Assessment Questionnaire-Disability Index, proportions of patients with pMDD/pGAD in those with baseline pMDD/pGAD, and American College of Rheumatology 20/50/70 response, and Disease Activity Score in 28 joints, erythrocyte sedimentation rate remission (< 2.6) rates.Results: A total of 4404 patients with non-missing baseline values were included. Baseline pMDD/pGAD was reported by 44.5%, 39.8%, 45.4%, and 39.1% of patients receiving tofacitinib 5 mg BID, tofacitinib 10 mg BID, adalimumab, and placebo, respectively. SF-36 MCS improvements were greater for tofacitinib versus adalimumab/placebo through month 6, with numerical improvements for tofacitinib versus adalimumab sustained through month 12, when the proportions of patients with baseline pMDD/pGAD who continued to have pMDD/pGAD were reduced. RA efficacy outcomes were generally similar in patients with/without baseline pMDD/pGAD.Conclusions: The percentage of patients with pMDD/pGAD reduced from baseline over 1 year of treatment with tofacitinib or adalimumab. Effective treatment of underlying RA may lead to improvements in depression and anxiety, based on the SF-36 MCS. Specially designed studies using gold-standard diagnostic tools would be warranted to investigate this further.Video Abstract available for this article.ConclusionsThe percentage of patients with pMDD/pGAD reduced from baseline over 1 year of treatment with tofacitinib or adalimumab. Effective treatment of underlying RA may lead to improvements in depression and anxiety, based on the SF-36 MCS. Specially designed studies using gold-standard diagnostic tools would be warranted to investigate this further.Video Abstract available for this article.
引用
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页码:35 / 50
页数:16
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