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Abstract Number: 593

Predictors of Persistence of Biologic Drug Step-Down Strategies in Inflammatory Arthritis: An Observational Study in Clinical Practice up to Seven Years of Follow-up

Sebastian C Rodriguez-Garcia1, Raul Castellanos-Moreira Sr.1, José Inciarte-Mundo2, M. Victoria Hernández3, Virginia Ruiz-Esquide2, Andrea Cuervo1, Julio Ramírez2, Juan Cañete1, Jose Gomez Puerta1 and Raimon Sanmartí1, 1Rheumatology Service, Hospital Clínic de Barcelona, Barcelona, Spain, 2Rheumatology, Hospital Clínic de Barcelona, Barcelona, Spain, 3Rheumatology, Hospital Clinic. Barcelona. Spain, Barcelona, Spain

Meeting: 2018 ACR/ARHP Annual Meeting

Keywords: Biologic drugs, Disease Sub-phenotyping, rheumatoid arthritis, treatment and spondylarthritis

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Session Information

Date: Sunday, October 21, 2018

Title: Rheumatoid Arthritis – Treatments Poster I: Strategy and Epidemiology

Session Type: ACR Poster Session A

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

Background/Purpose: Recommendations and guidelines for the management of Rheumatoid Arthritis (RA) and spondyloarthritis (SpA) with bDMARD include dose-tapering as an adequate option for patients on persistent remission. Although data regarding these strategies has increased in recent years, there is scarce evidence about their long-term effectiveness.

Our aim was to analyze the persistence of bDMARD dose-reduction in clinical practice and evaluate its predictors in patients with inflammatory arthritis with up to seven years of follow-up.

Methods: Prospective longitudinal study from June 2011 to April 2018. From a cohort of 153 patients with chronic inflammatory arthritis treated with bDMARD (TNF inhibitors, rituximab, tocilizumab, and abatacept) we recruited those with RA and SpA receiving reduced-dose regimens.1

Variables analyzed were: persistence of bDMARD dose-reduction, outcomes of patients requiring its withdrawal, predictors of persistence reported in the literature such as glucocorticoid (GC) and previous bDMARD use, disease activity and duration of disease at dose reduction as well as demographic and clinical features. A logistic regression model was used to identify factors associated with persistence on reduced-dose regimen after 7 years of follow-up

Results: 56 patients (RA:33; SpA:23) on tapered bDMARD (etanercept 51.8%, adalimumab 32.1%, Infliximab 3.6% and tocilizumab 12.5%) at study entry were included. Their clinical and laboratory features are shown in table 1.

After a mean follow-up on tapered-dose of 4.4 ± 2.6 years, 42.9% of subjects overall remained treated with this strategy (RA: 36.4%; SpA: 52.2%).

From those who required discontinuation of the step-down regimen, 15 (48.4%) achieved the therapeutic objective and 7 (22.6%) failed after returning to standard dose respectively. bDMARD were discontinued in 4 (12.9%) patients due to sustained disease remission (RA=3; SpA=1), 3 (9.7%) due to adverse events and 2 (6.4%) due to other reasons.

No significant differences in the different variables analyzed were found between patients continuing vs discontinuing reduced-dose regimens. Only disease duration at dose-reduction was associated with persistence of bDMARD step-down strategy overall (AOR: 1.13; 95% CI 1.01-1.26; p 0.02) in multivariate analysis.

Conclusion: A significant proportion of patients with RA and SpA (36.4% and 52.2% respectively) can be maintained with reduced doses of bDMARD after a long-term follow-up. Disease duration was the only predictor of dose-tapering persistence overall.

References:

1 Inciarte-Mundo J et al. Reumatol Clin. 2014;10(1):10–16

Table 1. Demographic and clinical features at bDMARD dose-reduction.

Total

n: 56

Continue tapered bDMARD

n: 24

Withdrawn tapered bDMARD

n:32

Age

52.3 ± 14.3

53.9 ± 13.9

51.1 ± 14.7

Female

32 (57.1%)

10 (41.7%)

22 (68.7%)

Smoking status

(ever smokers)

25%

23.8 %

26.1%

Diagnostics

RA

SpA

33

23

12 (36.4%)

12 (52.2%)

21 (63.6%)

11 (47.8%)

Mean disease duration (mean ± sd)

RA

SpA

14.4 ± 6.8

13.9 ± 6.3

18.5±7.9

13.9 ± 7.5

12.1 ± 4.9

13.9 ± 5

Disease activity (mean ± sd)

RA (DAS28)

AS (BASDAI)

2.3 ± 0.5

1.6 ± 1.6

2.3 ± 0.3

1.7 ± 1.8

2.3 ± 0.6

1.5 ± 1.7

Antibody Status (RA)

RF

ACPA

28 (85%)

29 (88%)

9 (75%)

9 (75%)

19 (90.5%)

20 (95.2%)

Number of positive Ab (RA)

0

1

2

4 (12%)

1 (3%)

28 (85%)

3 (25%)

0

9 (75%)

1 (4.7%)

1 (4.7%)

19 (90.5%)

Erosive disease (RA)

24/33

9/12

15/21

CRP (mg/dl) (median, IQR)

RA

SpA

0.05 (IQR:0.28)

0.06 (IQR:0.26)

0.07 (IQR:0.27)

0.03 (IQR:0.17)

0.05 (IQR:0.28)

0.06 (IQR:0.25)

ESR (median, IQR)

RA

SpA

9 (IQR:6)

10 (IQR:10)

9 (IQR:5)

7 (IQR:7)

9 (IQR:9)

12 (IQR: 8)

bDMARD Naive

RA

SpA

28 (85%)

17 (73.9%)

11 (91.7%)

9 (75%)

17 (81%)

8 (72.7%)

Concomitant csDMARD

RA

SpA

19 (57.6%)

5 (21.7%)

7 (58.3%)

1 (8.3%)

12 (55%)

4 (36.3%)

Concomitant GC

RA

SpA

8 (24.2%)

2 ( 9%)

2 (16.7%)

0

6 (28.6%)

2 (18.2%)


Disclosure: S. C. Rodriguez-Garcia, None; R. Castellanos-Moreira Sr., None; J. Inciarte-Mundo, None; M. V. Hernández, None; V. Ruiz-Esquide, None; A. Cuervo, None; J. Ramírez, None; J. Cañete, None; J. Gomez Puerta, None; R. Sanmartí, None.

To cite this abstract in AMA style:

Rodriguez-Garcia SC, Castellanos-Moreira R Sr., Inciarte-Mundo J, Hernández MV, Ruiz-Esquide V, Cuervo A, Ramírez J, Cañete J, Gomez Puerta J, Sanmartí R. Predictors of Persistence of Biologic Drug Step-Down Strategies in Inflammatory Arthritis: An Observational Study in Clinical Practice up to Seven Years of Follow-up [abstract]. Arthritis Rheumatol. 2018; 70 (suppl 9). https://acrabstracts.org/abstract/predictors-of-persistence-of-biologic-drug-step-down-strategies-in-inflammatory-arthritis-an-observational-study-in-clinical-practice-up-to-seven-years-of-follow-up/. Accessed .
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