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Abstract Number: 976

The Reason of Discontinuation of a First TNF Inhibitor Affects Drug Retention of a Second Anti-TNF Agent in Axial Spondyloarthritis

Adrian Ciurea1, Pascale Exer2, Ulrich Weber3,4, Giorgio Tamborrini5, Beate Steininger1, Rudolf O. Kissling6, Jürg Bernhard7 and Almut Scherer8, 1Rheumatology, University Hospital Zurich, Zurich, Switzerland, 2Private rheumatology practice, Basel, Switzerland, 3Institute of Regional Health Research, University of Southern Denmark, Odense, Denmark, 4Department of Research, King Christian 10th Hospital for Rheumatic Diseases, Graasten, Denmark, 5Department of Rheumatology, University Hospital, Zurich, Switzerland, 6Division of Rheumatology, Balgrist University Hospital, Zurich, Switzerland, 7Rheumatology and Rehabilitation, Bürgerspital Solothurn, Solothurn, Switzerland, 8SCQM Foundation, Zurich, Switzerland

Meeting: 2015 ACR/ARHP Annual Meeting

Date of first publication: September 29, 2015

Keywords: axial spondyloarthritis

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Session Information

Date: Sunday, November 8, 2015

Title: Spondylarthropathies and Psoriatic Arthritis - Clinical Aspects and Treatment: Treatment of AS

Session Type: ACR Concurrent Abstract Session

Session Time: 2:30PM-4:00PM

Background/Purpose: Conflicting results have been
demonstrated in axial spondyloarthritis (axSpA) with regard to whether
effectiveness of a second (2°) TNFi depends on the reason of discontinuation of
the first (1°) TNFi.

Methods: Patients with a clinical diagnosis of axSpA initiating a 2°
TNFi in the Swiss Clinical Quality Management (SCQM) cohort were included. 2°
TNFi drug maintenance and the proportion of patients achieving a moderately
active or inactive disease state according to defined Ankylosing Spondylitis
Disease Activity Score (ASDAS) cut-offs at 1 year (±6mo) were compared by the
reason of discontinuation of the 1° TNFi (primary or secondary lack of response
(PLR or SLR, defined as discontinuation of the 1° TNFi due to insufficient
effectiveness before or after 6 months, respectively), adverse events (AE) or
other reasons). LUNDEX values were used to indicate the proportion of patients
adhering to treatment and achieving a response criterion.

Results: A 2° TNFi was started in 591 patients after inclusion into
SCQM. Drug retention of 2° TNFi stratified by the reason of discontinuation of
the 1° TNFi  was significantly reduced after PLR in comparison to all other
reasons of discontinuation, log-rank p<0.001 (Figure 1). Median (IQR) drug
retention after PLR and SLR were 0.94 (0.58; 2.13) and 3.92 (2.46; 3.20) years,
respectively. The proportion of patients achieving an ASDAS <2.1 and
<1.3, respectively, in patients still on treatment (n=384) with complete
follow-up visits at 1 year (n=176) are shown in Table 1. Response rates were
slightly lower in patients having previously experienced PLR and AE in
comparison to SLR and highest in patients having switched due to “other”
reasons (e.g. remission, personal preferences). These differences were partially
more pronounced after LUNDEX adjustment. An ASDAS<1.3 was reached by 2-12%
of patients following a previous PLR, SLR or AE.

Conclusion: Previous PLR is associated with a strongly reduced retention
of the 2° TNFi. Only a minority of patients on a 2° TNFi having previously
experienced PLR, SLR or AE achieve an inactive disease state at 1 year. These
findings might help guiding treatment choices after discontinuation of a 1°
TNFi, as new treatment options with other modes of action will be available.

Table 1. Proportion of patients on a second TNFi
achieving a moderately active  or inactive

               disease state after 1 year (with and
without LUNDEX adjustement of treatment

               responses for drop-outs). #Fisher’s
test; µNon-parametric permutation test.

 

 

All

N=176

PLR

N = 35

SLR

N= 87

AE

N=36

Other

N=18

P

Value

ASDAS<2.1

40%

34%

43%

31%

61%

0.16#

ASDAS<2.1 LUNDEX

28%

19%

31%

21%

44%

0.11µ

ASDAS<1.3

14%

13%

16%

3%

28%

0.052#

ASDAS<1.3 LUNDEX

10%

8%

12%

2%

20%

0.055µ

 


Disclosure: A. Ciurea, Abbvie, 2,Abbvie, 5,Celgene, 5,Eli Lilly and Company, 5,Janssen Pharmaceutica Product, L.P., 5,MSD, 2,MSD, 5,Novartis Pharmaceutical Corporation, 5,Pfizer Inc, 2,Pfizer Inc, 5,UCB, 2,UCB, 5; P. Exer, None; U. Weber, Abbvie, 5,MSD, 5; G. Tamborrini, None; B. Steininger, None; R. O. Kissling, None; J. Bernhard, MSD, 5,Pfizer Inc, 5; A. Scherer, None.

To cite this abstract in AMA style:

Ciurea A, Exer P, Weber U, Tamborrini G, Steininger B, Kissling RO, Bernhard J, Scherer A. The Reason of Discontinuation of a First TNF Inhibitor Affects Drug Retention of a Second Anti-TNF Agent in Axial Spondyloarthritis [abstract]. Arthritis Rheumatol. 2015; 67 (suppl 10). https://acrabstracts.org/abstract/the-reason-of-discontinuation-of-a-first-tnf-inhibitor-affects-drug-retention-of-a-second-anti-tnf-agent-in-axial-spondyloarthritis/. Accessed .
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