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Rituximab treatment of adults with primary focal segmental glomerulosclerosis

To evaluate the efficacy and safety of rituximab (RTX) in the treatment of primary focal segmental glomerulosclerosis (FSGS) in adults. The clinical data of patients with primary FSGS who received RTX treatment in the First Affiliated Hospital of Zhengzhou University were analyzed retrospectively. T...

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Autores principales: Wang, Liuwei, Yu, Lu, Wang, Yulin, Guo, Yanhong, Zhai, Zihan, Tang, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130152/
https://www.ncbi.nlm.nih.gov/pubmed/37185370
http://dx.doi.org/10.1038/s41598-023-33678-y
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author Wang, Liuwei
Yu, Lu
Wang, Yulin
Guo, Yanhong
Zhai, Zihan
Tang, Lin
author_facet Wang, Liuwei
Yu, Lu
Wang, Yulin
Guo, Yanhong
Zhai, Zihan
Tang, Lin
author_sort Wang, Liuwei
collection PubMed
description To evaluate the efficacy and safety of rituximab (RTX) in the treatment of primary focal segmental glomerulosclerosis (FSGS) in adults. The clinical data of patients with primary FSGS who received RTX treatment in the First Affiliated Hospital of Zhengzhou University were analyzed retrospectively. The selected patients received RTX twice or four times, with a single dose of 375 mg/m(2), and the interval between two times of administration of RTX was 2–4 weeks. The treatment target is to achieve the clearance of B cells (peripheral blood B cell count < 5/μl). The primary outcome measures were remission and recurrence of renal disease, and the secondary outcome measures were adverse events and renal outcomes. A total of 14 FSGS patients were included, including 12 males, 9 with glucocorticoid-dependent or frequently relapsing nephrotic syndrome, and 3 with newly diagnosed nephrotic syndrome. After RTX treatment, 7 patients with glucocorticoid-dependent/recurrent nephrotic syndrome were completely relieved. At 6 months of follow-up, glucocorticoids were discontinued in all patients except 1 patient. The other 5 patients achieved partial remission (PR), of which 1 patient relapsed after PR, and 1 initial patient achieved complete remission. One patient progressed to end-stage renal disease (ESRD) after 4 months of follow-up. RTX in the treatment of adult glucocorticoid-dependent/relapsing FSGS can reduce the risk of recurrence and help to decline or discontinue the use of glucocorticoid and immunosuppressants.
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spelling pubmed-101301522023-04-27 Rituximab treatment of adults with primary focal segmental glomerulosclerosis Wang, Liuwei Yu, Lu Wang, Yulin Guo, Yanhong Zhai, Zihan Tang, Lin Sci Rep Article To evaluate the efficacy and safety of rituximab (RTX) in the treatment of primary focal segmental glomerulosclerosis (FSGS) in adults. The clinical data of patients with primary FSGS who received RTX treatment in the First Affiliated Hospital of Zhengzhou University were analyzed retrospectively. The selected patients received RTX twice or four times, with a single dose of 375 mg/m(2), and the interval between two times of administration of RTX was 2–4 weeks. The treatment target is to achieve the clearance of B cells (peripheral blood B cell count < 5/μl). The primary outcome measures were remission and recurrence of renal disease, and the secondary outcome measures were adverse events and renal outcomes. A total of 14 FSGS patients were included, including 12 males, 9 with glucocorticoid-dependent or frequently relapsing nephrotic syndrome, and 3 with newly diagnosed nephrotic syndrome. After RTX treatment, 7 patients with glucocorticoid-dependent/recurrent nephrotic syndrome were completely relieved. At 6 months of follow-up, glucocorticoids were discontinued in all patients except 1 patient. The other 5 patients achieved partial remission (PR), of which 1 patient relapsed after PR, and 1 initial patient achieved complete remission. One patient progressed to end-stage renal disease (ESRD) after 4 months of follow-up. RTX in the treatment of adult glucocorticoid-dependent/relapsing FSGS can reduce the risk of recurrence and help to decline or discontinue the use of glucocorticoid and immunosuppressants. Nature Publishing Group UK 2023-04-25 /pmc/articles/PMC10130152/ /pubmed/37185370 http://dx.doi.org/10.1038/s41598-023-33678-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Liuwei
Yu, Lu
Wang, Yulin
Guo, Yanhong
Zhai, Zihan
Tang, Lin
Rituximab treatment of adults with primary focal segmental glomerulosclerosis
title Rituximab treatment of adults with primary focal segmental glomerulosclerosis
title_full Rituximab treatment of adults with primary focal segmental glomerulosclerosis
title_fullStr Rituximab treatment of adults with primary focal segmental glomerulosclerosis
title_full_unstemmed Rituximab treatment of adults with primary focal segmental glomerulosclerosis
title_short Rituximab treatment of adults with primary focal segmental glomerulosclerosis
title_sort rituximab treatment of adults with primary focal segmental glomerulosclerosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130152/
https://www.ncbi.nlm.nih.gov/pubmed/37185370
http://dx.doi.org/10.1038/s41598-023-33678-y
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