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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.
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页码:35 / 50
页数:16
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