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Real-World Evidence Assessing Psoriatic Arthritis by Disease Domain: An Evaluation of the CorEvitas Psoriatic Arthritis/Spondyloarthritis Registry
被引:3
|作者:
Mease, Philip J.
[1
,2
]
O'Brien, Jacqueline
[3
]
Middaugh, Nicole
[3
]
Kricorian, Gregory
[4
]
Stryker, Scott
[4
]
Collier, David H.
[4
]
Ogdie, Alexis
[5
]
机构:
[1] Providence St Joseph Hlth, Swedish Med Ctr, Seattle, WA 98122 USA
[2] Univ Washington Sch Med, Seattle, WA 98195 USA
[3] CorEvitas LLC, Waltham, MA USA
[4] Amgen Inc, Thousand Oaks, CA USA
[5] Univ Penn, Perelman Sch Med, Philadelphia, PA USA
关键词:
DOUBLE-BLIND;
PLUS METHOTREXATE;
CONTROLLED TRIAL;
NAIVE PATIENTS;
SECUKINUMAB;
ADALIMUMAB;
GOLIMUMAB;
EFFICACY;
SAFETY;
SYMPTOMS;
D O I:
10.1002/acr2.11556
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
ObjectiveReal-world studies assessing treatment response by psoriatic arthritis (PsA) domains are limited. This study aimed to describe the patient characteristics, frequency and combinations of disease domains, disease activity, and patient-reported outcomes (PROs) by PsA domains in patients who initiated treatment with a tumor necrosis factor inhibitor (TNFi) or interleukin-17 inhibitor (IL-17i). MethodsAdults with PsA who initiated treatment with a TNFi or an IL-17i between January 2013 and January 2021 and had a 6 (& PLUSMN;3)-month follow-up were included. The prevalence of PsA domains, the most common domain combinations, treatment persistence, and unadjusted change in disease activity and PROs from baseline to 6 months for each PsA domain were summarized descriptively. ResultsOf the 1005 eligible patients, 63% were receiving TNFi and 37% were receiving IL-17i. Forty percent of TNFi and 14% of IL-17i initiators received these treatments as first-line therapy. Peripheral arthritis and skin disease were the most common PsA domains identified in 86% and 82% of patients, respectively, and the triad of peripheral arthritis, skin disease, and nail psoriasis was the most common domain combination observed in 14% of patients. More than two thirds (68%) of patients remained on therapy at 6 months' follow-up. Improvements in disease activity and PROs were observed across all PsA domains in those receiving TNFi or IL-17i. ConclusionThis real-world analysis highlights the heterogeneity in domain presentation; therefore, assessing all PsA domains is important for optimal disease management. Improvements in outcomes across all PsA domains demonstrate the effectiveness of TNFi and IL-17i in diverse patient groups exhibiting different phenotypes of PsA.
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页码:388 / 398
页数:11
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