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: 2285

Treatment of Adult Juvenile Idiopathic Arthritis Patients with Biologic Agents. Data from the National Registry

Katerina Jarosova1, Lenka Szczukova2, Zlatuse Kristkov3 and Jiri Vencovsky4, 1Institute of Rheumatology, Prague, Czech Republic, 2Institute of Biostatistics and Analyses. Faculty of Medicine, Masaryk University, Brno, Czech Republic, 3Institute of Biostatistics and Analyses, Faculty of Medicine, Masaryk University, Brno, Czech Republic, 4Institute of Rheumatology, Prague 2, Czech Republic

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: Biologic agents, juvenile idiopathic arthritis-enthesitis (ERA) and registry

  • Tweet
  • Email
  • Print
Session Information

Date: Tuesday, November 7, 2017

Title: Pediatric Rheumatology – Clinical and Therapeutic Aspects Poster III: Juvenile Arthritis

Session Type: ACR Poster Session C

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

Background/Purpose: To analyze the efficacy and safety of biologic agents in adult patients with juvenile idiopathic arthritis (JIA).

Methods:

ATTRA is a Czech national registry of patients with different forms of chronic arthritis who are treated with biologics. We have used this registry to evaluate treatment with TNF antagonists and other biologics in adult patients with juvenile idiopathic arthritis. Patients were treated with doses recommended for rheumatoid arthritis patients. Those patients, who failed to improve in DAS28 by at least 1.2 after 3 months at 2 consecutive visits, who lost the response during the treatment, or who had to be discontinued due to adverse event, were switched to alternative TNF inhibitor or other biologic drug. Clinical efficacy was assessed by the improvement in DAS28 and by assessment of quality of life using standard questionnaires (HAQ, SF36). Survival on therapy with biologic agent was calculated. Safety assessments were done for all patients during the whole follow-up period in 3 months intervals.

Results:

There are 419 adult patients with JIA followed in the ATTRA registry. Seventy-four started the treatment with biologic before 16 year of age; the remaining 345 commenced biologics in adult age. Valid and complete data for analysis are available in 275 patients, who have begun treatment in adulthood.

At the start of the treatment with biologics the mean age was 27±9 years, duration of disease 16±10 years and 73.8% were females. Mean age at the diagnosis was 11±6 years.

Patients were of the following subtypes of JIA: JIA RF negative 28.3%, JIA RF+ 22.8%, enthesitis related arthritis 18.9%, extended oligoarthritis 12.2%, psoriatic arthritis 7.2%, systemic onset 6,1% and persistent oligoarthritis 4.4%. The first biologic was either infliximab (37.1%), or etanercept (26.2%), adalimumab 27.6%), golimumab (4.4%), certolizumab (2.5%), tocilizumab (1.5%), abatacept (0,4%) and rituximab (0.4%).

Efficacy of the first biologic (DAS28):

DAS28

Before treatment

3 months

1 year

5 years

10 years

Mean±SD

5.7±1.0

3.1±1.1

2.8±1.2

2.4±1.1

2.5±1.4

Median

5.; 95.perc

5.7

(4.0; 7.2)

3.0

(1.4; 5.2)

2.7

(1.2; 4.9)

2.2

(1.1; 4.5)

2.1

(1.2;6.0)

Remission

2 (0.7%)

82 (34.2%)

91 (47.6%)

61 (64.2%)

23 (69.7%)

LDA

4 (1.5%)

56 (23.3%)

36 (18.8%)

15 (15.8%)

3 (9.1%)

Number of patients

275

240

191

95

33

Efficacy of long term treatment including switches (DAS28):

DAS28

Before treatment

3 month

1 year

5 years

10 years

Mean±SD

5.7±1.0

3.1±1.2

2.9±1.3

2.7±1.3

2.8±1.4

Median

5.; 95.perc

5.7

(4.0; 7.2)

3.1

(1.4; 5.2)

2.8

(1.2; 5.3)

2.5

(1.2; 5.4)

2.4

(1.2;6.0)

Remission

2 (0.7%)

83 (33.5%)

96 (45.1%)

86 (51.8%)

40 (53.3%)

LDA

4 (1.5%)

56 (22.6%)

42 (19.7%)

25 (15.1%)

13 (17.3%)

Number of patients

275

248

213

166

75

Conclusion:

A significant number of adult JIA patients benefit from long-term treatment with biological agents. DAS28 showed excellent and persistent improvement for patients maintaining first biologic up to 10 years. Treatment effect to second and other biologic agents was only slightly smaller and contributed to a very good persistence on the treatment. The effect on activity was mirrored also in the functional improvements assessed by HAQ.

Supported by Research Project from Ministry of Health in the Czech Republic No: 000 000 23728


Disclosure: K. Jarosova, None; L. Szczukova, None; Z. Kristkov, None; J. Vencovsky, None.

To cite this abstract in AMA style:

Jarosova K, Szczukova L, Kristkov Z, Vencovsky J. Treatment of Adult Juvenile Idiopathic Arthritis Patients with Biologic Agents. Data from the National Registry [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/treatment-of-adult-juvenile-idiopathic-arthritis-patients-with-biologic-agents-data-from-the-national-registry/. Accessed .
  • Tweet
  • Email
  • Print

« Back to 2017 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/treatment-of-adult-juvenile-idiopathic-arthritis-patients-with-biologic-agents-data-from-the-national-registry/

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