• Eur. J. Clin. Invest. · Dec 2015

    Comparative Study

    A new rescue regimen with plasma exchange and rituximab in high-risk membranous glomerulonephritis.

    • Janina Müller-Deile, Lena Schiffer, Marcus Hiss, Hermann Haller, and Mario Schiffer.
    • Division of Nephrology and Hypertension, Department of Medicine, Hannover Medical School, Hannover, Germany.
    • Eur. J. Clin. Invest. 2015 Dec 1; 45 (12): 1260-9.

    BackgroundEven though current treatment guidelines for idiopathic membranous glomerulonephritis (iMGN) exist, many questions regarding an optimal therapy remain unanswered. Complete remission cannot be achieved in all patients; relapses occur, in some cases frequently, and side effects from the immunosuppressive therapy are common. Therapeutic options in high-risk patients not responding to standard immunosuppressive therapies are limited. Recent research reveals that the human M-type phospholipase A2 receptor (PLA2 R) is a causative factor in iMGN that parallels clinical disease activity. However, in some patients, this correlation is not evident and additional undetermined factors seem to play a role.DesignWe evaluated a new rescue protocol including plasma exchanges (PE) against albumin, intravenous immunoglobulins (IVIGs) and rituximab for 10 patients with a biopsy-proven diagnosis of iMGN who were therapy-resistant to all conventional regimens and had a urinary protein to creatinine ratio of more than 10 000 mg/g Crea. We compared this protocol with standard immunosuppressive protocols including monthly alternating prednisolone plus cyclophosphamide (18 patients), cyclosporine plus prednisolone (23 patients) and rituximab alone (eight patients) in a retrospective design.ResultsOur rescue regimen with PE, IVIGs and rituximab achieved partial remission in 90% of patients who had been otherwise refractory to therapy. The mean time to partial remission was 2·1 months. Furthermore, two anti-PLA2 R-antibody negative patients were also treated with this rescue regimen, achieving partial remission after 1 and 4 months.ConclusionA combination of PE, IVIGs and rituximab is a treatment option to consider for high-risk patients with iMGN who are refractory to conventional therapy.© 2015 Stichting European Society for Clinical Investigation Journal Foundation.

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