Abstract

Aim To evaluate the efficacy and safety of MMF in jo-SLE in a multicenter study. Methods Medical charts of 26 pts, 25 F, 1 M, mean age at SLE diagnosis 12.7 yrs (range 5–18), mean age at MMF starting 15.9 yrs (range 7.5–26.8), followed in Florence, Padua, and Messina, Italy, treated with MMF from 2004 to 2007, were retrospectively analyzed. Clinical and laboratory evaluation included: blood count, ESR, CRP, ANA, anti-dsDNA, LFT, coagulation, C4, renal function, Coombs' test, aCL, anti?2GPI and LAC at baseline and every 6 months. Disease activity was monitored by the SLEDAI score. Treatment duration was 24 ± 14.8 months (range 2–52). MMF (1.5–2 g/day) was started due to steroid toxicity (n = 9 pts), CyA toxicity (n = 5), disease activity (n = 8) or nephropathy progression despite previous immunosuppression (n = 4). 9/26 pts, before MMF had renal disease (7 WHO Class IIb, 1 Class III, 1 Class IV). In 5/9 MMF was the first treatment, while 4/9 had received immunosuppressants. Results MMF was effective in reducing disease activity, steroid sparing in 14/26 (54%), stabilizing the disease in 8 (31%) and ineffective in 4 (15%). In 9/13 (69%) without renal involvement a good response was registered. Among pts with renal involvement, MMF was effective in 5/13 (38%), partially effective in 4 (31%) and ineffective in 4 (31%). 2 pts stopped MMF for diarrhoea and abdominal pain. Conclusion MMF seems to be effective and safe in jo-SLE, especially in patients without renal involvement. SLEDAI scores were significantly reduced at 6 and 12 months; p < 0.05.

Highlights

  • FF Falcini*1, CS Capannini1, MG Martini2, LTF La Torre3, VA Vitale3, NF Nacci1, MCM Matucci Cerinic1, CR Cimaz4 and ZF Zulian2

  • 15th Paediatric Rheumatology European Society (PreS) Congress Wietse Kuis, Patricia Woo, Angelo Ravelli, Hermann Girschick, Michaël Hofer, Johannes Roth, Rotraud K Saurenmann, Alberto Martini, Pavla Dolezova, Janjaap van der Net, Pierre Quartier, Lucy Wedderburn and Jan Scott Meeting abstracts – A single PDF containing all abstracts in this Supplement is available here.

  • Disease activity was monitored by the SLEDAI score

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Summary

Introduction

FF Falcini*1, CS Capannini1, MG Martini2, LTF La Torre3, VA Vitale3, NF Nacci1, MCM Matucci Cerinic1, CR Cimaz4 and ZF Zulian2. Mycophenolate Mofetil (MMF) for the treatment of juvenile onset systemic lupus erythematosus Address: 1Department of Biomedicine, Division of Rheumatology, Transition Unit, University of Florence, Florence, Italy, 2Department of Paediatrics, Rheumatology Unit, University of Padua, Padua, Italy, 3Department of Paediatrics, Rheumatology Unit, University of Messina, Messina, Italy and 4A. Meyer Children's Hospital, Rheumatology Unit, University of Florence, Florence, Italy

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