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The comparative efficacy and safety of anti-CD20 monoclonal antibodies for relapsing-remitting multiple sclerosis: A network meta-analysis

With the recent successful targeting of B lymphocytes in patients with multiple sclerosis (MS), treatment with anti-CD20 monoclonal antibodies (mAbs) may represent a promising managemental approach, particularly for those with relapsing/remitting MS (RRMS). A network meta-analysis was conducted base...

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Autores principales: Asha, Mohammad Z.I., Al-Asaad, Yousef, Khalil, Sundos F.H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8411244/
https://www.ncbi.nlm.nih.gov/pubmed/34505112
http://dx.doi.org/10.1016/j.ibneur.2021.08.003
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author Asha, Mohammad Z.I.
Al-Asaad, Yousef
Khalil, Sundos F.H.
author_facet Asha, Mohammad Z.I.
Al-Asaad, Yousef
Khalil, Sundos F.H.
author_sort Asha, Mohammad Z.I.
collection PubMed
description With the recent successful targeting of B lymphocytes in patients with multiple sclerosis (MS), treatment with anti-CD20 monoclonal antibodies (mAbs) may represent a promising managemental approach, particularly for those with relapsing/remitting MS (RRMS). A network meta-analysis was conducted based on a comprehensive search in Embase, PubMed, and the Cochrane Library to assess the comparative efficacy and safety of currently available anti-CD20 monoclonal antibodies (mAbs), including rituximab, ocrelizumab, and ofatumumab, versus a common comparator (interferon beta-1a [INFβ-1a]) in RRMS patients recruited in randomized clinical trials (RCTs). In a frequentist network meta-analytical model, annualized relapse rates (ARRs) and safety outcomes were expressed as risk ratios (RRs), whereas relapse-free events were expressed as odds ratios (ORs). Treatment ranking was performed using P-scores. The certainty of evidence was appraised using the GRADE approach. Five publications reported the outcomes of seven RCTs (3938 patients, 67.09% females). Compared to INFβ-1a, ocrelizumab reduced the risk of ARR (RR = 0.56, 95% CI, 0.50–0.64), serious adverse events (RR = 0.17, 95% CI, 0.09–0.30), and treatment discontinuation due to adverse events (SAEs, RR = 0.60, 95% CI, 0.39–0.93), and it was associated with higher odds of no relapses (OR = 2.47, 95% CI, 2.00–3.05). Ocrelizumab ranked best among all other treatments in terms of reducing ARR and SAEs. The quality of evidence was low for ocrelizumab, low to moderate for rituximab, and high for ofatumumab. Further large-sized, well-designed RCTs are needed to corroborate the efficacy and safety of ocrelizumab and other anti-CD20 mAbs in RRMS.
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spelling pubmed-84112442021-09-08 The comparative efficacy and safety of anti-CD20 monoclonal antibodies for relapsing-remitting multiple sclerosis: A network meta-analysis Asha, Mohammad Z.I. Al-Asaad, Yousef Khalil, Sundos F.H. IBRO Neurosci Rep Article With the recent successful targeting of B lymphocytes in patients with multiple sclerosis (MS), treatment with anti-CD20 monoclonal antibodies (mAbs) may represent a promising managemental approach, particularly for those with relapsing/remitting MS (RRMS). A network meta-analysis was conducted based on a comprehensive search in Embase, PubMed, and the Cochrane Library to assess the comparative efficacy and safety of currently available anti-CD20 monoclonal antibodies (mAbs), including rituximab, ocrelizumab, and ofatumumab, versus a common comparator (interferon beta-1a [INFβ-1a]) in RRMS patients recruited in randomized clinical trials (RCTs). In a frequentist network meta-analytical model, annualized relapse rates (ARRs) and safety outcomes were expressed as risk ratios (RRs), whereas relapse-free events were expressed as odds ratios (ORs). Treatment ranking was performed using P-scores. The certainty of evidence was appraised using the GRADE approach. Five publications reported the outcomes of seven RCTs (3938 patients, 67.09% females). Compared to INFβ-1a, ocrelizumab reduced the risk of ARR (RR = 0.56, 95% CI, 0.50–0.64), serious adverse events (RR = 0.17, 95% CI, 0.09–0.30), and treatment discontinuation due to adverse events (SAEs, RR = 0.60, 95% CI, 0.39–0.93), and it was associated with higher odds of no relapses (OR = 2.47, 95% CI, 2.00–3.05). Ocrelizumab ranked best among all other treatments in terms of reducing ARR and SAEs. The quality of evidence was low for ocrelizumab, low to moderate for rituximab, and high for ofatumumab. Further large-sized, well-designed RCTs are needed to corroborate the efficacy and safety of ocrelizumab and other anti-CD20 mAbs in RRMS. Elsevier 2021-08-27 /pmc/articles/PMC8411244/ /pubmed/34505112 http://dx.doi.org/10.1016/j.ibneur.2021.08.003 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Asha, Mohammad Z.I.
Al-Asaad, Yousef
Khalil, Sundos F.H.
The comparative efficacy and safety of anti-CD20 monoclonal antibodies for relapsing-remitting multiple sclerosis: A network meta-analysis
title The comparative efficacy and safety of anti-CD20 monoclonal antibodies for relapsing-remitting multiple sclerosis: A network meta-analysis
title_full The comparative efficacy and safety of anti-CD20 monoclonal antibodies for relapsing-remitting multiple sclerosis: A network meta-analysis
title_fullStr The comparative efficacy and safety of anti-CD20 monoclonal antibodies for relapsing-remitting multiple sclerosis: A network meta-analysis
title_full_unstemmed The comparative efficacy and safety of anti-CD20 monoclonal antibodies for relapsing-remitting multiple sclerosis: A network meta-analysis
title_short The comparative efficacy and safety of anti-CD20 monoclonal antibodies for relapsing-remitting multiple sclerosis: A network meta-analysis
title_sort comparative efficacy and safety of anti-cd20 monoclonal antibodies for relapsing-remitting multiple sclerosis: a network meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8411244/
https://www.ncbi.nlm.nih.gov/pubmed/34505112
http://dx.doi.org/10.1016/j.ibneur.2021.08.003
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