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
相关论文
共 50 条
  • [41] Effect of tofacitinib on dactylitis and patient-reported outcomes in patients with active psoriatic arthritis: post-hoc analysis of phase III studies
    Orbai, Ana-Maria
    Mease, Philip J.
    Helliwell, Philip S.
    FitzGerald, Oliver
    Fleishaker, Dona L.
    Mundayat, Rajiv
    Young, Pamela
    [J]. BMC RHEUMATOLOGY, 2022, 6 (01)
  • [42] Efficacy of tofacitinib on enthesitis in patients with active psoriatic arthritis: analysis of pooled data from two phase 3 studies
    Philip J. Mease
    Ana-Maria Orbai
    Oliver FitzGerald
    Mohamed Bedaiwi
    Rajiv Dona L. Fleishaker
    Pamela Mundayat
    Philip S. Young
    [J]. Arthritis Research & Therapy, 25
  • [43] Efficacy of tofacitinib on enthesitis in patients with active psoriatic arthritis: analysis of pooled data from two phase 3 studies
    Mease, Philip J.
    Orbai, Ana-Maria
    FitzGerald, Oliver
    Bedaiwi, Mohamed
    Fleishaker, Dona L.
    Mundayat, Rajiv
    Young, Pamela S.
    Helliwell, Philip
    [J]. ARTHRITIS RESEARCH & THERAPY, 2023, 25 (01)
  • [44] Efficacy and Safety of Tofacitinib in an Open-Label, Long-Term Extension Study in Patients with Psoriatic Arthritis Who Received Adalimumab or Tofacitinib in a Phase 3 Randomized Controlled Study: A Post Hoc Analysis
    Gladman, Dafna
    Nash, Peter
    Mease, Philip J.
    FitzGerald, Oliver
    Masri, Karim R.
    Duench, Stephanie
    Jane Cadatal, Mary
    [J]. ARTHRITIS & RHEUMATOLOGY, 2023, 75 : 2798 - 2801
  • [45] Joint-specific Responses to Tofacitinib and Adalimumab in Patients with Psoriatic Arthritis: Post Hoc Analysis of a Phase 3 Study
    Ciurea, Adrian
    Killeen, Tim
    Micheroli, Raphael
    Gassman, Norina N.
    Jo, Hyejin
    Kwok, Kenneth
    Kudlacz, Elizabeth
    Distler, Oliver
    Ospelt, Caroline
    Frank-Bertoncelj, Mojca
    [J]. ARTHRITIS & RHEUMATOLOGY, 2021, 73 : 2811 - 2814
  • [46] EFFICACY OF ADALIMUMAB AND TOFACITINIB IN RHEUMATOID ARTHRITIS: POST-HOC ANALYSES FROM A PHASE 3 STUDY
    van Vollenhoven, R.
    Cohen, S.
    Mendelsohn, A.
    Bananis, E.
    Fan, H.
    Takiya, L.
    Fleischmann, R.
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 2016, 75 : 1042 - 1042
  • [47] Impact of Tofacitinib on Components of the ACR Response Criteria: Post Hoc Analysis of Phase III and Phase IIIb/IV Trials
    Bessette, Louis
    Mysler, Eduardo
    Kinch, Cassandra D.
    Kwok, Kenneth
    Lukic, Tatjana
    On, Phu Vinh
    van Vollenhoven, Ronald F.
    [J]. JOURNAL OF RHEUMATOLOGY, 2022, 49 (06) : 566 - 576
  • [48] A post hoc analysis of two Phase III trials showing efficacy and tolerability of ceftobiprole in East Asian patients
    Huang, Haihui
    Gao, Lei
    Engelhardt, Marc
    Saulay, Mikael
    Hamed, Kamal
    [J]. FUTURE MICROBIOLOGY, 2020, 16 (11) : 783 - 796
  • [49] EFFICACY OF UPADACITINIB IN PATIENTS WITH PSORIATIC ARTHRITIS STRATIFIED BY BASELINE SKIN SEVERITY: A SUBGROUP ANALYSIS OF TWO PHASE III TRIALS
    Merola, J. F.
    Richette, P.
    Lubrano, E.
    Drescher, E.
    Soto, L.
    Lovan, C.
    Kato, K.
    Lippe, R.
    Lane, M.
    Kishimoto, M.
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 2021, 80 : 786 - 787
  • [50] Efficacy of Upadacitinib in Patients with Psoriatic Arthritis Stratified by Baseline Skin Severity: A Subgroup Analysis of Two Phase III Trials
    Joseph, Merola F.
    Pascal, Richette
    Ennio, Lubrano
    Edit, Drescher
    Lilian, Soto
    Charlie, Lovan
    Koji, Kato
    Ralph, Lippe
    Michael, Lane
    Mitsumasa, Kishimoto
    [J]. SWISS MEDICAL WEEKLY, 2021, 151 : S24 - S24