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Abstract Number: 834

The Efficacy of Rituximab in Systemic Sclerosis Joint Disease: A Pilot Study

Helena Borrell Paños1, Javier Narváez2, Juan José Alegre3, Ivan Castellvi4, Gloria Albert Espi3, Sergi Heredia1, Elide Toniolo4 and Joan Miquel Nolla1, 1Department of Rheumatology, Hospital Universitario de Bellvitge, Barcelona, Spain, 2Rheumatology, Hospital Universitario de Bellvitge, Barcelona, Spain, 3Rheumatology Department, Hospital Universitario Doctor Peset, Valencia, Spain, 4Rheumatology Unit. Hospital de la Santa Creu i Sant Pau, Barcelona, Spain

Meeting: 2015 ACR/ARHP Annual Meeting

Date of first publication: September 29, 2015

Keywords: Arthritis, rituximab and scleroderma

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Session Information

Date: Sunday, November 8, 2015

Title: Systemic Sclerosis, Fibrosing Syndromes and Raynaud's - Clinical Aspects and Therapeutics Poster I

Session Type: ACR Poster Session A

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

Background/Purpose:

Between 16 and 20% of patients with systemic sclerosis (SS) have arthritis, which is occasionally erosive. In addition, between 1 and 5% of patients show syndrome overlap with rheumatoid arthritis (RA).

The initial management of this complication is typically similar to RA, with the use of methotrexate as a first-choice DMARD. In refractory cases, anti-TNF therapies could be useful. However, many of these patients develop diffuse interstitial lung disease (DILD), which contraindicates the use of these drugs.

Our objective was to evaluate the efficacy and safety of rituximab (RTX) in the treatment of joint disease in patients with SS.

Methods:

An ambispective study of 13 patients with SS (ACR/EULAR 2013 criteria) and severe polyarticular disease treated with RTX was performed. The primary efficacy outcome was an improvement of joint counts, as evaluated by DAS28-ESR at the end of the follow-up period

Results:

Of the 13 patients included (12 women), seven (54%) had diffuse SS and six had a limited form of the disease. The mean age (± SD) was 54 ± 11 years, and the time of evolution (median) was 7 ± 12 years. Two (15%) patients had positive ACPA and fulfilled the criteria for RA classification. The baseline DAS28-ESR score was 6.4 ± 1.8.

The main clinical characteristics and response to treatment are shown in the following table.  

Indication DAS28 at the beginning Time tracking (months) Number of cycles DAS28 at last visit Previous treatments
Polyarthritis + DILD 6.55 12 2 2.21 MTX, LEF, Etanercept
Polyarthritis (overlap RA) 6.47 18 3 3.01 MTX, LEF, D-penicilamina
Polyarthritis 6.61 18 3 2.45 MTX, LEF, D-penicilamina
Polyarthritis + DILD 7.92 18 3 2.31 CFM, MMF
Polyarthritis 6.78 12 2 2.41 MTX, SZP, MMF
Polyarthritis 7.88 6 1 6.66 MTX, SZP, LEF, HCQ
Polyarthritis 7.05 18 3 3.43 MTX, CFM, SZP, MMF
Polyarthritis + DILD 4.47 27 4 3.06 MMF
Polyarthritis + DILD 4.38 16 2 1.89 MMF
Polyarthritis + DILD + calcinosis 3.39 16 2 2.52 MMF
Polyarthritis + DILD + severe skin disease 4.85 48 4 2.12 MMF, Imatinib
Polyarthritis + DILD + severe skin disease + calcinosis 4.36 24 4 3.20 CFM
Polyarthritis + DILD 3.49 30 3 1.19 CFM, MMF

RTX treatment was only ineffective in one patient (8%) and was suspended at six months because of ineffectiveness. In the remaining 12 patients (92%), a good control of joint counts was achieved, and at the end of the follow-up period (median ± SD) of 18 ± 10 months (range, 12-48), the mean DAS28-ESR score decreased to 2.8 ± 1.3 (% improvement: mean -46.89%; range, -70.83% to -15.48%). In eight patients (61%), joint disease remission (DAS28 < 2.6) was achieved. Three patients (23%) had low activity (DAS28 ≤ 3.2), and one (8%) had moderate activity.

The frequency of adverse effects was low, occurring in only two (15%) patients: one patient had two episodes of transient neutropenia (one feverish, prompting hospitalization), and the other had several mild infections (gastroenteritis, a urinary tract infection, and a respiratory infection). In neither of the two cases was it necessary to discontinue RTX treatment. In the patients with concomitant DILD, no worsening was observed in lung function tests. 

Conclusion:

In our experience, RTX is a safe and effective drug for the treatment of joint disease in patients with SS


Disclosure: H. Borrell Paños, None; J. Narváez, None; J. J. Alegre, None; I. Castellvi, None; G. Albert Espi, None; S. Heredia, None; E. Toniolo, None; J. M. Nolla, None.

To cite this abstract in AMA style:

Borrell Paños H, Narváez J, Alegre JJ, Castellvi I, Albert Espi G, Heredia S, Toniolo E, Nolla JM. The Efficacy of Rituximab in Systemic Sclerosis Joint Disease: A Pilot Study [abstract]. Arthritis Rheumatol. 2015; 67 (suppl 10). https://acrabstracts.org/abstract/the-efficacy-of-rituximab-in-systemic-sclerosis-joint-disease-a-pilot-study/. Accessed .
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