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Abstract Number: 2379

Minimal Radiographic Progression in RA Patients Receiving Routine Care in the Espoir Early Arthritis Cohort: Similar Prognosis According to 6 Different Remission Criteria

Isabel Castrejón1, Maxime Dougados2, Bernard Combe3, Francis Guillemin4, Bruno Fautrel5 and Theodore Pincus1, 1Rheumatology, Rush University Medical Center, Chicago, IL, 2Université Paris René Descartes and Hôpital Cochin, Paris, France, 3Immuno-Rhumatologie, Hôpital Lapeyronie, Montpellier, France, 4Nancy University Hospital, Nancy, France, 5Rheumatology, UPMC GRC08, Paris 06 University, Pitié Salpétrière Hospital, Paris, France

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: Disease Activity, prognostic factors and remission

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Session Information

Title: Rheumatoid Arthritis - Clinical Aspects (ACR): Impact of Various Interventions and Therapeutic Approaches

Session Type: Abstract Submissions (ACR)

Background/Purpose

Remission has become a more achievable goal in rheumatoid arthritis (RA). Several criteria for remission are available in RA, including one based on RAPID3 (routine assessment of patient index data 3) with <1 swollen joint (RAPID3≤3+SJ≤1), which identifies remission similarly to Boolean and SDAI criteria [1]. It would be of value to know if any remission criteria predict radiographic progression more effectively than others.  We analyzed radiographic progression according to remission status in the ESPOIR French early arthritis cohort, in which only 18.3% of patients received a biological DMARD over a 5 year follow-up as part of their routine care [2].

Methods

Radiographic progression over 1 year was analyzed in the ESPOIR cohort, which includes early arthritis patients who received routine care. Remission was assessed 12 months after baseline, according to 6 different criteria: ACR Boolean criteria; simplified disease activity index (SDAI) ≤3.3; clinical disease activity index (CDAI) ≤2.8; disease activity score (DAS28) <2.6; RAPID3 ≤3; and RAPID3≤3+SJ≤1.The numbers of patients whose radiographic progression according to the Sharp van der Heijde score was ≥5 -the smallest detectable difference (SDD) [3], ≥10 or ≥20 units at 24 months (12 months after the remission assessment) were analyzed, according to whether patients had been in remission 12 months earlier for each of the 6 criteria, using chi-square tests for statistical significance.

Results

Radiographic progression ≥5 units (SDD) was seen in 10.1%-11.8% of patients in remission compared to 13.0%-13.8% of patients not in remission; differences were not statistically significant (p>0.3) (Table). Progression ≥10 units was seen in 1.4-4.3% of patients in remission versus 6.5-7.6% of those not in remission, a 2-fold difference; only differences by DAS28 and RAPID3≤3+SJ≤1 were statistically significant (p<0.05). Progression ≥20 units was seen in 0.1-1.1% of those in remission versus 2.6-3.1% of those not in remission, a 3-fold difference, statistically significant for SDAI, CDAI, DAS28 and RAPID3≤3+SJ≤1.  A sub analysis including 179 patients with radiographic damage at baseline and rheumatoid factor positivity was performed, with similar results.  

 

Remission Criteria

 

Remission vs Non remission

Radiographic progression (%) over 1 year according to remission status

≥ 5 units

≥ 10 units

≥ 20 units

Remission

No Remission

Remission

No Remission

Remission

No Remission

Boolean

140 vs 492

10.9%

13.0%

3.6%

6.5%

0%

2.6%

SDAI ≤ 3.3

135 vs 467

10.4%

13.3%

3.0%

6.9%

0%

2.8%*

CDAI ≤ 2.8

135 vs 467

10.4%

13.3%

3.0%

6.9%

0%

2.8%*

DAS28 ≤ 2.6

247 vs 355

10.9%

13.8%

3.6%

7.6%*

0.8%

3.1%*

RAPID3 ≤ 3

187 vs 415

11.8%

13.0%

4.3%

6.8%

1.1%

2.7%

RAPID3≤3+SJ≤1

139 vs 463

10.1%

13.4%

1.4%

7.3%*

0%

2.8%*

*p ≤ 0.05

Conclusion

Very little radiographic progression was seen in patients receiving routine care in recent years although only 18.3% of patients received a biological agent. Differences between patients in remission or non become apparent when applying higher cut-off points to define radiographic progression.

References: 1. J Rheumatol 2013;40:386-93. 2. J Rheumatol 2013;40:1650-7 3.Arthritis Rheum 2002;46:913–20


Disclosure:

I. Castrejón,
None;

M. Dougados,
None;

B. Combe,

Roche France,

2;

F. Guillemin,
None;

B. Fautrel,
None;

T. Pincus,
None.

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