Abstract

IntroductionThis study aimed to describe treatment changes (discontinuation, switching, and therapy add-on) following the initiation of biologic or nonbiologic oral disease-modifying antirheumatic drugs (DMARDs) in psoriatic arthritis (PsA) patients.MethodsAdult patients with ≥2 PsA diagnoses from physician office visits, initiated on a biologic or nonbiologic oral DMARD, were selected from the Truven Health Analytics MarketScan® Research Database (2005 to 2009). Patients were required to have continuous insurance coverage ≥6 months prior to and ≥12 months post index date (first prescription fill date). Treatment discontinuation, treatment switch, and therapy add-on were captured over the 1 year period following the index date. Treatment changes were described separately for patients initiated on nonbiologic and biologic DMARDs.ResultsA total of 1,698 and 3,263 patients were initiated on an oral nonbiologic DMARD and biologic DMARD respectively. For patients initiated on nonbiologic DMARDs, 69% had ≥1 therapy change over the 12 month study period (median time 85 days). Among patients who had a therapy change, 83% discontinued, 29% switched therapy (64% switched to a biologic DMARD), and 25% had a therapy add-on (76% added-on with a biologic DMARD). For patients initiated on a biologic DMARD, 46% had ≥1 therapy change (median time 110 days). Among patients who had a therapy change, 100% discontinued, 25% switched therapy (92% switched to another biologic DMARD), and 7% had a therapy add-on with a nonbiologic DMARD.ConclusionThis study suggests that PsA patients newly initiated on a nonbiologic/biologic DMARD do not remain on the index treatment for a long period of time. A better understanding of factors related to these early treatment changes in PsA patients is needed.

Highlights

  • This study aimed to describe treatment changes following the initiation of biologic or nonbiologic oral disease-modifying antirheumatic drugs (DMARDs) in psoriatic arthritis (PsA) patients

  • Treatment patterns were reported separately for patients initiated on an oral nonbiologic DMARD, on a biologic DMARD, and for patients from the MTX subgroup

  • Overall, 1,698 patients met the sample selection criteria and initiated an oral nonbiologic DMARD on the index date, with the majority being initiated on MTX (71%, n = 1,217)

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Summary

Introduction

This study aimed to describe treatment changes (discontinuation, switching, and therapy add-on) following the initiation of biologic or nonbiologic oral disease-modifying antirheumatic drugs (DMARDs) in psoriatic arthritis (PsA) patients. Psoriatic arthritis (PsA), an idiopathic, chronic, and often progressive immune-mediated autoinflammatory arthritis, affects peripheral and axial joints, nails and entheses, and is typically accompanied by psoriatic skin lesions [1,2]. PsA symptoms typically include joint pain, stiffness, swelling, nail psoriasis, dactylitis and generalized fatigue [1,3]. The immediate treatment goals in PsA include mitigating joint pain and swelling, skin lesions, disease progression, and systemic sequelae [3,4]. Pharmacotherapy for PsA encompasses nonsteroidal anti-inflammatory drugs (NSAIDs) and intra-articular corticosteroid injections to manage musculoskeletal pain, stiffness, and swelling, as well as nonbiologic and biologic disease-modifying antirheumatic drugs (DMARDs), which have the potential to attenuate joint damage and promote disease remission [6]

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