Persistence and Adherence Among Patients with Psoriatic Arthritis Treated with Targeted Immune Modulators
Author(s)
Walsh JA1, Cai Q(2, Lin I3, Pericone CD4, Chakravarty SD3
1University of Utah, Salt Lake City, UT, USA, 2Janssen Scientific Affairs, LLC, Newtown, PA, USA, 3Janssen Scientific Affairs, LLC, Horsham, PA, USA, 4Janssen Scientific Affairs, LLC, Titusville, NJ, USA
OBJECTIVES: To compare treatment adherence and persistence among PsA patients initiating TNFi, IL-12/23i, IL-17i or tsDMARDs. METHODS: Adults with ≥1 medical or pharmacy claim for a TNFi, IL-12/23i, IL-17i or tsDMARD during 10/1/2013–10/31/2018 were selected from IBM MarketScan® Commercial and Medicare Supplemental Databases. Date of first claim was the index date. Patients were required to have ≥12 months pre-index and ≥12 months post-index continuous enrollment, ≥2 PsA diagnoses ≥30 days apart during this 24-month period, and a PsA diagnosis on/ prior to index date. Patients with ≥2 study medications on the same day, other biologic-indicated autoimmune conditions, contraindications, or any study medication prior to the index date were excluded. Pairwise propensity score matching was performed. Proportion of Days Covered (PDC), duration of persistence, and number of patients discontinuing index biologic (i.e., gap between fills >1.5 times maintenance days’ supply) were compared between matched cohorts. RESULTS: Of 7,205 patients meeting identification criteria, there were 238 matched patient pairs for TNFi vs. IL-12/23i; 238 pairs for tsDMARDs vs. IL-12/23i; and 189 pairs for IL-17i vs. IL-12/23i. Patient characteristics were similar between cohorts. Duration of persistence was higher for the IL-12/23i cohort than for TNFi (269 vs 215 days, p<0.01) or tsDMARDs (269 vs 214 days, p<0.01), but comparable with IL‑17i. The IL-12/23i cohort had fewer index treatment discontinuations than the TNFi (53.4% vs 73.9%, p<0.01) or tsDMARDs (53.4% vs 71.8%, p<0.01) cohorts, but no significant difference with IL‑17i. During the 12-month follow-up period, patients initiating IL-12/23i had higher mean PDC than those on TNFi (0.64 vs 0.56, p<0.01) or tsDMARDs (0.64 vs 0.58, p=0.03), but similar to those on IL‑17i. CONCLUSIONS: In this real-world study of PsA therapies with differing mechanisms of action, IL-12/23i demonstrated higher treatment adherence and longer persistence versus both TNFi and tsDMARDs, and comparability to IL-17i.
Conference/Value in Health Info
2021-05, ISPOR 2021, Montreal, Canada
Value in Health, Volume 24, Issue 5, S1 (May 2021)
Code
PSY23
Topic
Patient-Centered Research
Topic Subcategory
Adherence, Persistence, & Compliance
Disease
Systemic Disorders/Conditions