Efficacy and safety of tofacitinib by background methotrexate dose in psoriatic arthritis: post hoc exploratory analysis from two phase III trials

被引:7
|
作者
Kivitz, Alan J. [1 ]
FitzGerald, Oliver [2 ]
Nash, Peter [3 ]
Pang, Shirley [4 ]
Azevedo, Valderilio F. [5 ]
Wang, Cunshan [6 ]
Takiya, Liza [7 ]
机构
[1] Altoona Ctr Clin Res, Dept Rheumatol, Duncansville, PA USA
[2] Univ Coll, Conway Inst Biomol Res, Dept Rheumatol, Dublin, Ireland
[3] Griffith Univ, Sch Med, Brisbane, Qld, Australia
[4] St Joseph Heritage Healthcare, Fullerton, CA USA
[5] Univ Fed Parana, Curitiba, Parana, Brazil
[6] Pfizer Inc, Groton, CT 06340 USA
[7] Pfizer Inc, Collegeville, PA 19426 USA
关键词
Disease activity; Disease-modifying anti-rheumatic drugs; Methotrexate; Psoriatic arthritis; Tofacitinib; PREVALENCE; RECOMMENDATIONS; EPIDEMIOLOGY; THERAPY; PLACEBO;
D O I
10.1007/s10067-021-05894-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective Analyze tofacitinib efficacy and safety by background methotrexate (MTX) dose in patients with psoriatic arthritis (PsA). Methods This post hoc analysis pooled data from two phase III, double-blind trials (OPAL Broaden, NCT01877668; OPAL Beyond, NCT01882439) including patients receiving tofacitinib 5 or 10 mg twice daily (BID), or placebo, with stable MTX. Efficacy outcomes at month 3 stratified by MTX dose (<= 15 month 3 stratified by MTX dose vs > 15 mg/week) were American College of Rheumatology (ACR)20/50/70, Health Assessment Questionnaire-Disability Index (HAQ-DI); Psoriasis Area and Severity Index (PASI)50/75; change from baseline in HAQ-DI; physician's global assessment of PsA (PGA-PsA-visual analog scale [VAS]); patient's global joint and skin assessment (PGJS-VAS), Leeds Enthesitis Index (LEI); and Dactylitis Severity Score (DSS). Safety assessments included adverse events and laboratory parameters. Results Five hundred fifty-six patients received tofacitinib 5 mg BID (n = 186), 10 mg BID (n = 178), or placebo (n = 192), plus MTX (<= 15 mg/week, n = 371; > 15 mg/week, n = 185). At month 3, tofacitinib efficacy was generally greater than placebo. Patients receiving tofacitinib 5 mg BID demonstrated greater numerical improvements in efficacy outcomes at month 3 with MTX > 15 mg/week vs MTX <= 15 mg/week; patients receiving tofacitinib 10 mg BID displayed the opposite. The safety profile was generally consistent between groups; headache was associated with MTX > 15 mg/week; decreased hemoglobin levels were observed in patients receiving tofacitinib 10 mg BID and MTX <= 15 mg/week. Conclusion Efficacy of tofacitinib was generally numerically greater than placebo, regardless of MTX dose. Tofacitinib 5 mg BID was generally more efficacious with MTX > 15 mg/week vs <= 15 mg/week; the opposite was observed for tofacitinib 10 mg BID. Headache was more frequent with MTX > 15 mg/week.
引用
收藏
页码:499 / 511
页数:13
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