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Abstract Number: 195

Inflammatory Arthritis in Patients with Myelodysplastic Syndrome: French Multicenter Retrospective Study

Arsene Mekinian1, Olivier Decaux2, Geraldine Falgarone3, Thorsten Braun Sr.4, Eric Toussirot5, Loic Raffray6, Bruno Gombert7, Bruno de Wazieres8, Anne Laure Buchdaul9, Jean-Marc Ziza10, David Launay11, Guillaume Denis12, Serge Madaule13, Pierre Fenaux14 and Olivier Fain15, 1Internal Medicine, Jean Verdier Hospital, Bondy, FL, France, 2Department of Internal Medicine, Rennes University Hospital, Rennes, France, 3Rheumatology, Hopital avicenne, Paris, France, 4Hematology, Avicenne hospital, Bobigny, France, 5Université de Franche Comté , CHRU, CIC Biotherapy 506 and Rheumatology and EA 4266 Pathogens and Inflammation, Besançon, France, 6Internal Medicine, CHU de Bordeaux, Bordeaux, France, 7Internal Medicine, La Rochelle hospital, La Rochelle, France, 8Internal Medecine, CHU de Nimes, Nimes, France, 9Internal Medicine, Douai hospital, Douai, France, 10Rheumatology, Croix Saint Simon Hospital, Paris, France, 11Internal Medicine, Claude Huriez University Hospital, Lille, France, 12Internal Medicine, Rochefoucault hospital, Rochefoucault, France, 13Rheuamtology, Albi hospital, Albi, France, 14Hematology, Avicenne Hospital, France, 15Internal Medicine, Jean Verdier Hospital, Bondy, France

Meeting: 2012 ACR/ARHP Annual Meeting

Keywords: Rheumatoid arthritis (RA)

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Session Information

Title: Miscellaneous Rheumatic and Inflammatory Diseases: Periodic Fever Syndromes

Session Type: Abstract Submissions (ACR)

Inflammatory arthritis in patients with myelodysplastic syndrome: French multicenter retrospective study.

For the Société Nationale Française de Médecine Interne (SNFMI), the CRI (Club Rhumatismes Inflammation) and Groupe Français d’étude des syndromes myélodysplasiques.

 

 

Background/Purpose :

To describe the characteristics and the outcome of inflammatory arthritis in patients with myelodysplastic syndrome (MDS).

Methods:

French multicenter retrospective study which included patients with MDS and inflammatory arthritis. Patient’s clinical, biological and radiological data at the diagnosis, during the follow-up were recorded, as well as treatment regimen. Patients with isolated arthritis were compared to MDS-associated vasculitis (n=22).

Results:

Twenty-two patients with myelodysplastic syndrome (77.5 years [69-81]; 10 women) were included. IPSS score of the myelodysplastic syndrome was 0.75 [0-1.4]. Inflammatory arthritis was present in all patients, with polyarthritis in 14 (64%) and symmetric involvement in 15 cases (68%). At the diagnosis of the arthritis, median DAS28-CRP was 4.5 [2-6.5], with the presence of anti-CCP antibodies in 2 cases (9%) and radiological erosions in 1 case. The median time between the diagnosis arthritis and MDS was of 9 [2-30] months, with median articular symptoms duration of 3 months [2-8]. The appearance of these 2 diseases was concomitant in 6 (27%) cases; arthritis preceded MDS in 12 (55%) and occurred after MDS in 4 (18%) cases. Characteristics of arthritis and of MDS, as well as treatments at the different points are in table 1. Whereas the number of swollen and tender joints significantly diminished during follow-up, as was the median DAS28-CRP (from 4.3 [3.8-4.6] at baseline to 2.9 [1.75-3.3]; p<0.05), C-reactive protein remained elevated (CRP>20 mg/l in 14 (64%) at baseline versus 8 (42%)). Nevertheless, no patients show any radiographic progression and new anti-CCP positivity during the follow-up of 29 [9-76] months. No correlation was found in concern the evolution of MDS and inflammatory arthritis. In concern the treatments, whereas almost all patients have corticosteroids, the associated treatment was present in only 4 cases (hydroxychloroquine in 2 cases, salazopyrine and etanercept, n=1; each). Eleven patients died during the follow-up from complications of MDS treatment or acutisation. In patients with MDS-associated vasculitis (n=22), death occurred in 17 cases (77%), but survival was not different from patients with only inflammatory arthritis.

Conclusion:

This study describes the characteristics of associated inflammatory arthritis in MDS. At the difference of other inflammatory arthritis, the use of other than steroids immunosuppressors is very poor, probably in relation with the underlying hemopathy. The use of biologics in this condition could be preferred to methotrexate, but need prospective studies.

 

Number of evaluable patients

Baseline

assessment

N=22

First visit

N=19

Second visit

N=11

Third visit

N=9

Last visit

N=19

Arthritis characteristics

 

 

 

 

 

Delay from the diagnosis (months)

–

6 [3-14]

14 [8-32]

19 [13-27]

38 [17-61]

Arthralgias

22 (100%)

13 (68%)**

6 (55%)**

3 (33%)**

9 (47%)**

Arthritis

16 (73%)

5 (26%)**

2 (18%)**

1 (11%)**

3 (16%)**

Number of swollen joints

6 [4-8]

2 [0-4]**

4 [0-4]*

0 [0-3]**

0 [0-4.5]**

Number of tender joints

3 [0-4.5]

0 [0-2]**

0 [0-1]*

0 [0]*

0 [0]**

Morning stiffness (hours)

1 [0-1]

0 [0-0.5]**

0 [0-0.5]**

0 [0-0.5]*

0 [0]**

Erosion present

1 (5%)

1 (5%)

–

–

1 (5%)

C-reactive protein (mg/l)

30 [10-58]

10 [5-30]*

25 [3.5-56]

25 [8-140]

10 [3.5-55]

CRP>20 mg/l

14 (64%)

7 (37%)

5 (45%)

4 (44%)

8 (42%)

DAS28-CRP

4.3 [3.8-4.6]

3 [1.8-3.7]**

2.7 [2.2-4]*

2.8 [1.6-3.3]**

2.9 [1.75-3.3]**

Efficacy (by physician)

 

15 (79%)

7 (64%)

6 (67%)

15 (79%)

RA treatments

 

 

 

 

 

Corticosteroids (prednisone)

16 (73%)

12 (63%)

10 (91%)

8 (89%)

14 (74%)

Corticosteroids (prednisone; mg/day

27.5 [16-35]

15 [10-25]

10 [9.5-20]

9.5 [5-17]*

8 [5-15]**

Steroid dependence

–

5 (26%)

4 (36%)

1 (11%)

2 (11%)

Other treatments

4 (18%)

hydroxychloroquine

 (n=2)

etanercept

salazopyrin

4 (21%) hydroxychloroquine (n=2)

etanercept

salazopyrin

3 (27%) hydroxychloroquine (n=2)

salazopyrin

2 (22%) hydroxychloroquine

4 (21%)

hydroxychloroquine (n=3)

anakinra

MDS characteristics

 

 

 

 

 

Hemoglobin (g/dl)

9 [8-11]

11 [8.5-11.5]

11 [8.7-13]

10 [8-11]

10 [8-12]

Platelets (n/mm3)

163 [62-657]

114 [50-242]

233 [75-250]

150 [40-244]

75 [12-146]*

Neutrophils (n/mm3)

260 [740-5070

1500 [1000-3000]

1300 [1150-2500]

1200 [1000-3105]

2300 [1000-4550]

Blastes  (%)

0 [0-8]

0 [2]

0 [0-0]

0 [0-2.5]

0 [0-1]

MDS aggravation

–

3 (16%)

2 (18%)

4 (44%)

4 (21%)

MDS treatment

4(18%)

6 (32%)

3 (27%)

3 (33%)

6 (32%)

*p<0.05 versus baseline

*p<0.005 versus baseline

 


Disclosure:

A. Mekinian,
None;

O. Decaux,
None;

G. Falgarone,
None;

T. Braun Sr.,
None;

E. Toussirot,
None;

L. Raffray,
None;

B. Gombert,
None;

B. de Wazieres,
None;

A. L. Buchdaul,
None;

J. M. Ziza,
None;

D. Launay,
None;

G. Denis,
None;

S. Madaule,
None;

P. Fenaux,
None;

O. Fain,
None.

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