Nefrotik sendromlu çocuklarda rituximab deneyimi, farklı ne gözlemledik?

Autor: İlknur GİRİŞGEN, Selçuk YÜKSEL, Yücel PEKAL
Jazyk: angličtina
Rok vydání: 2020
Popis: Aim: We aimed to evaluate the efficacy of rituximab therapy in childrenwith nephrotic syndromes and to share our experiences.Material and Methods: Twelve children with nephrotic syndrome (fourwith steroid-dependent, eight with steroid-resistant nephrotic syndrome) who were treated with rituximab were retrospectively evaluatedin terms of clinical and laboratory data and CD19-20 levels. All patientsreceived rituximab (375 mg/m2) once weekly for 4 weeks. A proteinuria-free period under steroid therapy was not sought prior to initiatingrituximab therapy.Results: The overall remission rates in patients with steroid-dependent and steroid-resistant nephrotic syndrome were 100% and 27%.Focal segmental glomerulosclerosis was diagnosed in six patients andthe remission rate was 33% in this population. CD19 cell depletion wasobserved in 10 of the 12 children. Seven of the 10 patients with CD19depletion achieved remission, whereas the other three had persistentnephrotic proteinuria despite CD19 depletion. Two patients withoutCD19 depletion never achieved remission. Relapse occurred in three ofthe seven patients associated with increased CD19.Conclusion: We observed that rituximab could be given without waitingfor a proteinuria-free period under steroid therapy. Our result suggestthat administering four weekly doses of rituximab increases the likelihood of remission, considering the amount of drug lost in the urineof children with nephrotic proteinuria. However, our findings must beconfirmed with dose-comparison studies conducted with larger populations and an evaluation of long-term adverse effects. Some patientsdid not achieve remission despite B cell depletion, which suggests thatB cell depletion is necessary but insufficient for remission in nephroticsyndromes.
Databáze: OpenAIRE