Serious infections in patients with self-reported psoriatic arthritis from the Psoriasis Longitudinal Assessment and Registry (PSOLAR) treated with biologics

被引:24
作者
Ritchlin, Christopher T. [1 ]
Stahle, Mona [2 ]
Poulin, Yves [3 ,4 ]
Bagel, Jerry [5 ]
Chakravarty, Soumya D. [6 ,7 ]
Kafka, Shelly [6 ]
Srivastava, Bhaskar [6 ]
Langholff, Wayne [8 ]
Gottlieb, Alice B. [9 ]
机构
[1] Univ Rochester, Div Allergy Immunol & Rheumatol, Med Ctr, 601 Elmwood Ave,Box 695, Rochester, NY 14642 USA
[2] Karolinska Inst, Karolinska Univ Hosp, Dept Med, Stockholm, Sweden
[3] Univ Laval, Quebec City, PQ, Canada
[4] Ctr Rech Dermatol Quebec Metropolitain, Quebec City, PQ, Canada
[5] Psoriasis Treatment Ctr Cent New Jersey, East Windsor, NJ USA
[6] Janssen Sci Affairs LLC, Horsham, PA USA
[7] Drexel Univ, Coll Med, Philadelphia, PA 19104 USA
[8] Janssen Res & Dev, Spring House, PA USA
[9] New York Med Coll, Metropolitan Hosp, New York, NY USA
关键词
PSOLAR; Psoriasis; Psoriatic arthritis; Serious infections; NECROSIS-FACTOR INHIBITORS; RHEUMATOID-ARTHRITIS; BRITISH-SOCIETY; FACTOR THERAPY; DOUBLE-BLIND; RISK; SAFETY; MULTICENTER; PHASE-3; AGENTS;
D O I
10.1186/s41927-019-0094-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundPatients with psoriatic arthritis (PsA) have increased risk of adverse events, including serious infections (SI), compared with psoriasis patients.MethodsPatients eligible for, or receiving conventional systemic and biologic agents for psoriasis were followed prospectively using PSOLAR. Cohorts included: ustekinumab, tumor necrosis factor (TNF) inhibitors; infliximab; etanercept; adalimumab; non-biologic/methotrexate (MTX) (reference group); and non-biologic/non-MTX. Multivariate analyses using Cox hazard regression were used to identify factors associated with time to first SI. Rates of SI in PSOLAR psoriasis patients with self-reported PsA and possible risks with biologic therapy were evaluated.ResultsPSOLAR enrolled 4315 psoriasis patients with self-reported PsA. The overall population (N=2401) included patients (n): 628 ustekinumab; 1413 TNF inhibitors; 258 infliximab; 481 etanercept; 674 adalimumab; 54 other biologics, 98 non-biologic/MTX; 208 non-biologic/non-MTX. Overall, 138 SI were reported with incidence rates per 100 patient-years as follows: a) ustekinumab: 1.00; b) TNF inhibitors: 2.22; c) infliximab: 2.12; d) etanercept: 2.58; e) adalimumab: 1.99; f) non-biologic/MTX: 3.01; g) and non-biologic/non-MTX: 2.31. Age, time-dependent disease activity Physician's Global Assessment (PGA) of 4, 5, history of infection, and diabetes were associated with increased risk for SI (p<0.05) in self-reported PsA patients. Biologic groups, other than ustekinumab, had numerically higher rates of SI.ConclusionsPSOLAR psoriasis patients with self-reported PsA in the TNF inhibitors, infliximab, adalimumab, etanercept, and MTX cohorts had numerically higher SI rates than the ustekinumab cohort, although not statistically significant. Age, PGA 4, 5, history of infection, and diabetes were associated with an increased risk for SI, irrespective of biologic exposure.Trial registrationNCT00508547; Registered July 30, 2007.
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页数:13
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