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Efficacy and safety of belimumab for the treatment of refractory childhood-onset systemic lupus erythematosus: A single-center, real-world, retrospective study

OBJECTIVE: This study aimed to investigate the efficacy and safety of belimumab for treating children with refractory childhood-onset systemic lupus erythematosus (cSLE). METHODS: Twenty-six cSLE patients who received belimumab treatment in our hospital from January 2020 to September 2021 (23 of the...

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Autores principales: Wang, Dahai, Shan, Chunrong, Liu, Jia, Zhang, Ranran, Zhu, Guohao, Gao, Tingting, Chang, Hong, Gao, Shan, Bai, Cui, Nie, Nana, Zhang, Qiuye, Lin, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9794867/
https://www.ncbi.nlm.nih.gov/pubmed/36591249
http://dx.doi.org/10.3389/fimmu.2022.1067721
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author Wang, Dahai
Shan, Chunrong
Liu, Jia
Zhang, Ranran
Zhu, Guohao
Gao, Tingting
Chang, Hong
Gao, Shan
Bai, Cui
Nie, Nana
Zhang, Qiuye
Lin, Yi
author_facet Wang, Dahai
Shan, Chunrong
Liu, Jia
Zhang, Ranran
Zhu, Guohao
Gao, Tingting
Chang, Hong
Gao, Shan
Bai, Cui
Nie, Nana
Zhang, Qiuye
Lin, Yi
author_sort Wang, Dahai
collection PubMed
description OBJECTIVE: This study aimed to investigate the efficacy and safety of belimumab for treating children with refractory childhood-onset systemic lupus erythematosus (cSLE). METHODS: Twenty-six cSLE patients who received belimumab treatment in our hospital from January 2020 to September 2021 (23 of them for more than 52 weeks) were enrolled in this study. Their clinical and laboratory data, assessment of disease activity, glucocorticoid dosage, and treatment-emergent adverse events (TEAEs) were retrieved for analysis. The paired samples t-test and the nonparametric test were used to compare the baseline and post-treatment data. RESULTS: The mean age of onset was 10.3 ± 2.4 years old; the mean disease duration was 41.6 ± 37.4 months; the median Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) score was 10 (P (25), P (75): 3, 17); and the mean Physician’s Global Assessment (PGA) score at baseline was 1.9 ± 1.0. Compared with the baseline values, there was a significant decrease in the 24-h urine protein quantifications at 24 and 52 weeks of treatment (P<0.05) as well as an elevated complement (C) 3 and C4 levels at 4, 12, 24, and 52 weeks of treatment. In addition, the SLEDAI-2K and PGA scores as well as the percentage of CD19(+) B cells were significantly decreased at 12, 24, and 52 weeks of treatment compared with the baseline values (P<0.05). The dosage of glucocorticoid at 4, 12, 24, and 52 weeks of treatment was significantly less than that at baseline or the previous follow-up (P<0.05). At 52 weeks, 14 subjects (53.8%) achieved Lupus Low Disease Activity State (LLDAS), and 4 subjects (15.4%) reached clinical remission (CR). At the last follow-up, 16 subjects (61.5%) achieved LLDAS, and 10 subjects (38.5%) reached CR. CONCLUSIONS: Belimumab treatment can significantly improve laboratory indicators, reduce disease activity, and decrease the dosage of glucocorticoid required in children with cSLE. Moreover, it has a good safety profile.
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spelling pubmed-97948672022-12-29 Efficacy and safety of belimumab for the treatment of refractory childhood-onset systemic lupus erythematosus: A single-center, real-world, retrospective study Wang, Dahai Shan, Chunrong Liu, Jia Zhang, Ranran Zhu, Guohao Gao, Tingting Chang, Hong Gao, Shan Bai, Cui Nie, Nana Zhang, Qiuye Lin, Yi Front Immunol Immunology OBJECTIVE: This study aimed to investigate the efficacy and safety of belimumab for treating children with refractory childhood-onset systemic lupus erythematosus (cSLE). METHODS: Twenty-six cSLE patients who received belimumab treatment in our hospital from January 2020 to September 2021 (23 of them for more than 52 weeks) were enrolled in this study. Their clinical and laboratory data, assessment of disease activity, glucocorticoid dosage, and treatment-emergent adverse events (TEAEs) were retrieved for analysis. The paired samples t-test and the nonparametric test were used to compare the baseline and post-treatment data. RESULTS: The mean age of onset was 10.3 ± 2.4 years old; the mean disease duration was 41.6 ± 37.4 months; the median Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) score was 10 (P (25), P (75): 3, 17); and the mean Physician’s Global Assessment (PGA) score at baseline was 1.9 ± 1.0. Compared with the baseline values, there was a significant decrease in the 24-h urine protein quantifications at 24 and 52 weeks of treatment (P<0.05) as well as an elevated complement (C) 3 and C4 levels at 4, 12, 24, and 52 weeks of treatment. In addition, the SLEDAI-2K and PGA scores as well as the percentage of CD19(+) B cells were significantly decreased at 12, 24, and 52 weeks of treatment compared with the baseline values (P<0.05). The dosage of glucocorticoid at 4, 12, 24, and 52 weeks of treatment was significantly less than that at baseline or the previous follow-up (P<0.05). At 52 weeks, 14 subjects (53.8%) achieved Lupus Low Disease Activity State (LLDAS), and 4 subjects (15.4%) reached clinical remission (CR). At the last follow-up, 16 subjects (61.5%) achieved LLDAS, and 10 subjects (38.5%) reached CR. CONCLUSIONS: Belimumab treatment can significantly improve laboratory indicators, reduce disease activity, and decrease the dosage of glucocorticoid required in children with cSLE. Moreover, it has a good safety profile. Frontiers Media S.A. 2022-12-14 /pmc/articles/PMC9794867/ /pubmed/36591249 http://dx.doi.org/10.3389/fimmu.2022.1067721 Text en Copyright © 2022 Wang, Shan, Liu, Zhang, Zhu, Gao, Chang, Gao, Bai, Nie, Zhang and Lin https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Wang, Dahai
Shan, Chunrong
Liu, Jia
Zhang, Ranran
Zhu, Guohao
Gao, Tingting
Chang, Hong
Gao, Shan
Bai, Cui
Nie, Nana
Zhang, Qiuye
Lin, Yi
Efficacy and safety of belimumab for the treatment of refractory childhood-onset systemic lupus erythematosus: A single-center, real-world, retrospective study
title Efficacy and safety of belimumab for the treatment of refractory childhood-onset systemic lupus erythematosus: A single-center, real-world, retrospective study
title_full Efficacy and safety of belimumab for the treatment of refractory childhood-onset systemic lupus erythematosus: A single-center, real-world, retrospective study
title_fullStr Efficacy and safety of belimumab for the treatment of refractory childhood-onset systemic lupus erythematosus: A single-center, real-world, retrospective study
title_full_unstemmed Efficacy and safety of belimumab for the treatment of refractory childhood-onset systemic lupus erythematosus: A single-center, real-world, retrospective study
title_short Efficacy and safety of belimumab for the treatment of refractory childhood-onset systemic lupus erythematosus: A single-center, real-world, retrospective study
title_sort efficacy and safety of belimumab for the treatment of refractory childhood-onset systemic lupus erythematosus: a single-center, real-world, retrospective study
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9794867/
https://www.ncbi.nlm.nih.gov/pubmed/36591249
http://dx.doi.org/10.3389/fimmu.2022.1067721
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