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: 0898

Inadequate Response Among Psoriatic Arthritis Patients Prescribed Advanced Therapy in a Real-world US Commercially Insured Population

Julie Birt1, Michael Grabner2, Keith Isenberg3, Theresa Hunter4, Chia-Chen Teng2, Mingyang Shan1, Jeffrey Lisse1, Jianmin Wu1, Kirstin Griffing1 and Jeffrey R Curtis5, 1Eli Lilly and Company, Indianapolis, IN, 2Healthcore, Inc, Wilmington, DE, 3Anthem, Inc, Indianapolis, IN, 4Eli Lilly and Company, Indianapolis, 5Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL

Meeting: ACR Convergence 2020

Keywords: Biologicals, 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

Date: Saturday, November 7, 2020

Title: Spondyloarthritis Including Psoriatic Arthritis – Treatment Poster II

Session Type: Poster Session B

Session Time: 9:00AM-11:00AM

Background/Purpose: The purpose of this analysis was to assess the frequency of inadequate response (IR) over 1 year associated with advanced therapy (AT) initiation among psoriatic arthritis (PsA) patients in the US using a claims-based algorithm that was originally developed and validated for rheumatoid arthritis1. Baseline factors associated with IR to AT were also analyzed.

Methods: This was a retrospective cohort study using claims data from the HealthCore Integrated Research Database®. Adult patients with PsA who initiated an AT (TNFi: adalimumab, certolizumab, etanercept, golimumab, infliximab; non-TNFi biologic: abatacept, ixekizumab, secukinumab, ustekinumab; other: apremilast, tofacitinib) from 7/1/2016 to 8/31/2018 and had continuous enrollment ≥6 months before and ≥12 months after index date (date of first biologic claim) were included. The index AT was defined as the first AT prescribed during the study time period. Patients were identified as having IR to their index AT if during the 12 months after index date (defined as date of first AT claim) they had one or more of the following: low adherence (defined as proportion of days covered (PDC)< 80%), switched/added a new AT, added a new conventional synthetic immunomodulator (e.g. methotrexate), increased dose/frequency of AT, had >1 glucocorticoid injection/infusion, addition or dose increase of oral glucocorticoids, used a new topical treatment, actinotherapy, or retinoids, or used a new pain medication. Baseline characteristics were compared between responders and IRs using Chi-squared tests for categorical variables and t-tests for continuous variables. A multivariable logistic regression model was constructed to identify baseline characteristics associated with IR to index AT.

Results: A total of 1,433 PsA patients were included in this analysis. Mean age was 49 years, 47% were male, 67% initiated a TNFi, 22% initiated other ATs, and 11% initiated a non-TNFi biologic (Table 1). Over the 1-year follow-up period, 77% of PsA patients had IR to their index AT: 63% of patients had low adherence, 21% switched/added a new AT, 9% added a new conventional synthetic immunomodulator, 3% had a dose/frequency increase of their index AT, 11% had >1 glucocorticoid injection/infusion, 7% had an addition/dose increase of oral glucocorticoids, 3% used a new topical treatment, actinotherapy or retinoids, and 12% used a new pain medication (Table 2). Inadequate responders were more likely to be female (odds ratio (OR)=1.37; p=0.017), have anxiety or depression (OR=1.80; p=0.002), and have a higher baseline Quan-Charlson Comorbidity Index (QCI) score (OR=1.21; p=0.036); while patients with baseline use of methotrexate were more likely to be responders (OR=0.72; p=0.015) (Table 3). Prior exposure to TNFi was associated with a 2.14-fold greater odds of non-response (p=0.003).

Conclusion: Over 75% of PsA patients had an IR to their index AT 1 year after initiation, mostly driven by low adherence and switching to or adding on a new treatment. Health plan claims data appears useful to classify inadequate responders in PsA, and additional research should be done to further validate this claims-based algorithm in a clinical setting.


Disclosure: J. Birt, Eli Lilly and Company, 1, 3; M. Grabner, None; K. Isenberg, Anthem, 1, 3, Anthem, 1, 3; T. Hunter, Eli Lilly and Company, 1, 3; C. Teng, None; M. Shan, Eli Lilly and Company, 3; J. Lisse, Eli Lilly and Company, 1, 3; J. Wu, Eli Lilly and Company, 1, 3; K. Griffing, Eli Lilly and Company, 1, 3; J. Curtis, AbbVie, 2, 5, Amgen, 2, 5, Bristol-Myers Squibb, 2, 5, Corrona, 2, 5, Janssen, 2, 5, Lilly, 2, 5, Myriad, 2, 5, Pfizer, 2, 5, Regeneron, 2, 5, Roche, 2, 5, UCB, 2, 5, Gilead Sciences, Inc., 5, Sanofi, 5.

To cite this abstract in AMA style:

Birt J, Grabner M, Isenberg K, Hunter T, Teng C, Shan M, Lisse J, Wu J, Griffing K, Curtis J. Inadequate Response Among Psoriatic Arthritis Patients Prescribed Advanced Therapy in a Real-world US Commercially Insured Population [abstract]. Arthritis Rheumatol. 2020; 72 (suppl 10). https://acrabstracts.org/abstract/inadequate-response-among-psoriatic-arthritis-patients-prescribed-advanced-therapy-in-a-real-world-us-commercially-insured-population/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to ACR Convergence 2020

ACR Meeting Abstracts - https://acrabstracts.org/abstract/inadequate-response-among-psoriatic-arthritis-patients-prescribed-advanced-therapy-in-a-real-world-us-commercially-insured-population/

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