ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 2234

US Treatment Patterns of Psoriatic Arthritis Patients Newly Initiated On Etanercept or Adalimumab

Frank Zhang1, Stan Li2 and Jeffrey R. Curtis3, 1Pricing and Market Access, I&I, Celgene Corporation, Warren, NJ, 2Pricing and Market Access, Celgene Corporation, Warren, NJ, 3Rheumatology & Immunology, Univ of Alabama-Birmingham, Birmingham, AL

Meeting: 2012 ACR/ARHP Annual Meeting

Keywords: Adalimumab, etanercept and psoriatic arthritis

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Title: Spondylarthropathies and Psoriatic Arthritis: Clinical Aspects and Treatment

Session Type: Abstract Submissions (ACR)

Background/Purpose: Etanercept (ETN) and Adalimumab (ADA) are commonly used biologic disease-modifying antirheumatic drugs (DMARDs) for psoriatic arthritis (PsA) patients (pts). However, little is known about subsequent treatment changes after the initiation of these two biologics. The objective of this study was to describe treatment patterns following the initiation of ETN and ADA in PsA patients in US in a real-world setting.

Methods: Adult PsA pts were selected from MarketScan Commercial Claims database (2005-2009). First ETN/ADA prescription date was defined as the index date. Pts were required to have continuous enrollment 6-month prior to (baseline period) and 12-month post index date (study period), no use of the index biologic treatment during baseline, have received ≥2 PsA diagnoses from physician office visits at any time over the 18-month period, with at least one PsA diagnosis during baseline period, and no diagnosis of ankylosing spondylitis. ETN/ADA combo therapy was defined as having at least 28 days of concomitant use of a non-biologic DMARD following the index date; otherwise ETN/ADA monotherapy was defined. Treatment patterns were captured over the 12-month study period and were defined as the following: complete treatment discontinuation — a treatment interruption of ≥60 consecutive days past the end of the days’ supply (discontinuation date) and no other DMARD therapy between the discontinuation date and the end of the study period; a switch in therapy — the initiation of a new non-biologic/biologic DMARD (not used during baseline) within 60 days of the discontinuation date; intermittent use of the index biologic — ≥60 days of treatment gap of the index biologic; step-down — discontinuation of one of the DMARD therapies among patients previously on combo therapy; step-up — adding another DMARD (not used during baseline) concomitantly with the index biologic for ≥28 consecutive days. Therapy modification was defined as any switch, intermittent use, step-down or step-up.

Results: A total of 2,037 and 2,217 PsA pts were newly initiated on ETN and ADA respectively, most on monotherapy (ETN: 69.2%, ADA: 67.5%). Over the 12-month study period, the majority of the pts had ≥ 1 therapy change (ETN: 65.3%, ADA: 69.1%), with median time to change 113 days and 112 days respectively. Among pts initiated on mono ETN/ADA, 40.7% ETN and 33.5% ADA pts remained on the index mono therapy. 12.1% ETN and 11.6% ADA pts discontinued the treatment, 18.2% ETN and 14.7% ADA pts had intermittent treatment, 7.0% ETN and 11.4% ADA pts switched to another mono therapy, and 21.9% ETN and 29.1% ADA pts step-up to combo therapy. Among pts initiated on ETN/ADA in combination with an oral DMARD, a proportion of pts remained on the original combo therapy (ETN: 21.4%, ADA: 26.8%). The majority of the patients ‘stepped down’ to monotherapy (ETN: 77.5%, ADA: 72.7%). Very few pts discontinued both drugs in the combo therapy (ETN: 0.5%, ADA: 0.1%) or adopting intermittent biologic therapy (ETN: 0.6%, ADA: 0.3%).

Conclusion: This study suggests that most of the PsA patients newly initiated on ETN or ADA have a therapy change over the first year. Both ‘step-up’ and ‘step down’ strategy are observed frequently.


Disclosure:

F. Zhang,

Celgene Corporation,

3;

S. Li,

Celgene ,

5;

J. R. Curtis,

Celgene ,

5.

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to 2012 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/us-treatment-patterns-of-psoriatic-arthritis-patients-newly-initiated-on-etanercept-or-adalimumab/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology