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: 404

Remission is a Difficult Target in Clinical Practice When RA Disease Is Established

Till Uhlig1, Elisabeth Lie2, Cecillie Kaufmann3, Erik Rødevand4, Knut Mikkelsen5, Synnøve Kalstad6 and Tore K. Kvien1, 1Dept. of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway, 2Rheumatology, Diakonhjemmet Hospital, Oslo, Norway, 3Rheumatology department, Vestre Viken, Drammen, Norway, 4Dept. of Rheumatology, St. Olavs Hospital, Trondheim, Norway, 5Lillehammer Hospital for Rheumatic Diseases, Lillehammer, Norway, 6Dept. of Rheumatology, University Hospital of Northern Norway, Tromsø, Norway

Meeting: 2012 ACR/ARHP Annual Meeting

Keywords: Disease-modifying antirheumatic drugs, remission and rheumatoid arthritis (RA)

  • 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: Rheumatoid Arthritis - Clinical Aspects I: Drug Studies/Drug Safety/Drug Utilization/Disease Activity & Remission

Session Type: Abstract Submissions (ACR)

Background/Purpose:

Clinical remission is the treatment target in rheumatoid arthritis (RA) and several composite indices are available for evaluation of remission and low disease activity (LDA) states. We currently have little information on how disease duration impacts remission and LDA rates in daily clinical practice. We examined how often clinical remission and LDA is achieved in clinical practice using existing definitions in RA patients with variable disease duration.

Methods:

Data were retrieved from the NOR-DMARD register. For the present analyses we used data from all 4568 patients starting with a synthetic (n=3095) or biological (n=1473) DMARD with available a 3-month follow-up data, and also from 3262 patients with available 6 months follow-up data. Mean (SD) age was 54.7 (13.7) yrs, disease duration was 8.5 (7.9) yrs, 72.7% of patients were females.

Applied definitions for clinical remission included the Disease Activity Score based on 28 joint counts (DAS28) <2.6, the Simplified Disease Activity Index (SDAI) <3.3, the Clinical Disease Activity Index (CDAI) <2.8, Routine Assessment of Patient Index Data (RAPID3, range 0-10) <1, and the ACR/EULAR remission definition (A/E) with tender joint count, swollen joint count, patient global assessment (scale 0-10), and CRP (mg/dL) all <1. We also explored a practical remission definition of A/E without CRP (A/E PRAC), and low disease activity for DAS28 (<3.2), SDAI (<11), CDAI (<10) and RAPID3 (<2). The four investigated categories for disease duration were: <1 year, 1<6 years, 6-10 years, and >10 years.

Results:

The table shows percentages for patients according to disease duration periods who met different remission and LDA definitions after 3 months and 6 months of DMARD treatment.

While the new A/E remission criteria were most stringent, for all remission indices the likelihood of remission after 3 and 6 months of DMARD treatment decreased with increasing RA disease duration (Chi square test p<0.01 for all comparisons for 3 and 6 months follow-up). Remission and low disease activity rates after 3 and 6 months were clearly best in patients with up to one year disease duration. Only 6-9 percent of patients with disease duration over 1 year achieved after 3-6 months DMARD treatment a state of remission according to the A/E criteria.

Disease duration (yrs)

All

<1

1-<6

6-<10

>10

All

<1

1-<6

6-<10

>10

 

Remission 3 months (%)

Remission 6 months (%)

DAS28

21.2

26.3

19.9

16.9

18.1

24.7

31.7

20.8

23.5

19.6

SDAI

8.9

12.6

7.6

7.7

6.0

10.8

14.4

10.2

8.8

8.0

CDAI

9.5

12.9

8.2

8.4

6.8

11.4

15.4

10.3

9.7

8.4

RAPID3

19.4

25.5

17.0

19.2

14.0

20.1

26.0

20.0

18.0

14.2

A/E

8.0

11.0

6.8

6.5

5.7

9.4

11.6

9.0

8.0

7.7

A/E PRACT

9.5

12.9

8.6

7.9

6.9

11.3

14.3

10.1

9.8

9.1

 

LDA 3 months (%)

LDA 6 months (%)

DAS28

34.0

39.9

32.2

30.5

30.3

39.7

47.5

38.0

35.0

34.3

SDAI

40.5

46.9

38.3

37.2

36.4

46.7

55.1

45.1

42.7

40.3

CDAI

41.0

47.0

38.5

37.4

37.9

47.3

55.0

45.8

43.2

41.6

RAPID3

38.7

46.8

36.6

36.3

32.4

40.7

48.5

40.2

37.7

33.6

Conclusion:

The target of remission varies in difficulty across different remission criteria and is less often achieved with increasing disease duration. These observations have implication for how treat-to-target can be managed in a realistic way in patients with established disease and may indicate that many patients with established disease will need an individualized target due to joint destruction, co-morbidities and other factors.


Disclosure:

T. Uhlig,
None;

E. Lie,
None;

C. Kaufmann,
None;

E. Rødevand,

Abbott Immunology Pharmaceuticals,

5,

Pfizer Inc,

5,

Roche Pharmaceuticals,

5,

UCB,

5;

K. Mikkelsen,
None;

S. Kalstad,
None;

T. K. Kvien,

Abbott Immunology Pharmaceuticals,

8,

AstraZeneca,

8,

Merck Pharmaceuticals,

8,

NiCox, S.A.,

8,

Pfizer Inc,

8,

Roche Pharmaceuticals,

8,

UCB,

8,

BMS,

5,

Abbott Immunology Pharmaceuticals,

5,

Merck Pharmaceuticals,

5,

NiCox, S.A.,

5,

Pfizer Inc,

5,

Roche Pharmaceuticals,

5,

UCB,

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/remission-is-a-difficult-target-in-clinical-practice-when-ra-disease-is-established/

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