Available Alternative Biologics and Disease Groups Influence Biologic Drug Survival in Patients with Psoriasis and Psoriatic Arthritis

BACKGROUNDFactors other than efficacy and safety could influence the survival of biologics in patients with psoriasis. Little is known about whether different disease groups affect drug survival of biologics or not. OBJECTIVEThis study aimed to investigate whether the availability of alternative bio...

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Published inAnnals of dermatology Vol. 34; no. 5; pp. 321 - 330
Main Authors Oh, Sohee, Choi, Sungjun, Yoon, Hyun-Sun
Format Journal Article
LanguageEnglish
Published The Korean Dermatological Association; The Korean Society for Investigative Dermatology 01.10.2022
대한피부과학회
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Summary:BACKGROUNDFactors other than efficacy and safety could influence the survival of biologics in patients with psoriasis. Little is known about whether different disease groups affect drug survival of biologics or not. OBJECTIVEThis study aimed to investigate whether the availability of alternative biologics and disease groups could influence drug survival of biologics approved for psoriasis and psoriasis arthritis (PsA). METHODSA nationwide population-based retrospective cohort study was conducted using the Health Insurance and Review Assessment data in Korea between January 2009 and August 2019. RESULTSThe drug survival analysis included 5,634 biologic episodes. Ustekinumab was the most frequently prescribed drug (n=2,488, 44.2%). Multivariable time-dependent Cox regression analysis showed that higher age, female sex, no comorbidity, concomitant cyclosporine or acitretin use, biologic-experienced and use of tumor necrosis factor (TNF)-α inhibitors were predictors of drug discontinuation. PsA was a predictor of drug persistence, particularly for TNF-α inhibitors. Ustekinumab and adalimumab discontinuation significantly increased after introducing secukinumab and ustekinumab, respectively. CONCLUSIONThe availability of alternative biologics and disease groups affect biologic drug survival in patients with psoriasis and PsA.
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ISSN:1013-9087
2005-3894
DOI:10.5021/ad.22.003