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Ofatumumab for B cell depletion therapy in ANCA-associated vasculitis: a single-centre case series

Objectives. B cell depletion is an effective treatment strategy in ANCA-associated vasculitis (AAV). Ofatumumab is a fully humanized anti-CD20 mAb that has shown efficacy in the treatment of haematological malignancy and RA. The use of ofatumumab in the treatment of AAV has not previously been repor...

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Autores principales: McAdoo, Stephen P., Bedi, Rachna, Tarzi, Ruth, Griffith, Megan, Pusey, Charles D., Cairns, Thomas D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4957674/
https://www.ncbi.nlm.nih.gov/pubmed/27094598
http://dx.doi.org/10.1093/rheumatology/kew199
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author McAdoo, Stephen P.
Bedi, Rachna
Tarzi, Ruth
Griffith, Megan
Pusey, Charles D.
Cairns, Thomas D.
author_facet McAdoo, Stephen P.
Bedi, Rachna
Tarzi, Ruth
Griffith, Megan
Pusey, Charles D.
Cairns, Thomas D.
author_sort McAdoo, Stephen P.
collection PubMed
description Objectives. B cell depletion is an effective treatment strategy in ANCA-associated vasculitis (AAV). Ofatumumab is a fully humanized anti-CD20 mAb that has shown efficacy in the treatment of haematological malignancy and RA. The use of ofatumumab in the treatment of AAV has not previously been reported. Methods. This study was based on a case series of eight patients who received ofatumumab, in conjunction with low-dose CYC and oral steroids, in the treatment of AAV. Results. Eight patients received ofatumumab: seven for remission induction in active disease (three relapsing; four with new disease) and one for remission maintenance. B cell depletion was achieved in all patients by 1 month, and was sustained for at least 6 months. All patients with active disease achieved clinical remission (BVAS of zero, or BVAS ⩽5 if all scores due to persistent urinary abnormalities in the presence of stable or improving renal function) by 3 months. This was associated with a rapid fall in ANCA titres, reduced inflammatory responses and improvements in renal function. At 12 months, three patients had repopulated B cells associated with the recurrence of circulating ANCAs, although no patients experienced major clinical relapse in the first 24 months. No unexpected side effects were observed. Conclusion. Treatment with ofatumumab resulted in similar serological and clinical responses to those seen in previous cohorts treated at our centre with a comparable CS, CYC and rituximab-based regimen. Ofatumumab should be considered an alternative B cell depleting agent in patients who are intolerant of, or unresponsive to, rituximab.
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spelling pubmed-49576742016-07-29 Ofatumumab for B cell depletion therapy in ANCA-associated vasculitis: a single-centre case series McAdoo, Stephen P. Bedi, Rachna Tarzi, Ruth Griffith, Megan Pusey, Charles D. Cairns, Thomas D. Rheumatology (Oxford) Clinical Science Objectives. B cell depletion is an effective treatment strategy in ANCA-associated vasculitis (AAV). Ofatumumab is a fully humanized anti-CD20 mAb that has shown efficacy in the treatment of haematological malignancy and RA. The use of ofatumumab in the treatment of AAV has not previously been reported. Methods. This study was based on a case series of eight patients who received ofatumumab, in conjunction with low-dose CYC and oral steroids, in the treatment of AAV. Results. Eight patients received ofatumumab: seven for remission induction in active disease (three relapsing; four with new disease) and one for remission maintenance. B cell depletion was achieved in all patients by 1 month, and was sustained for at least 6 months. All patients with active disease achieved clinical remission (BVAS of zero, or BVAS ⩽5 if all scores due to persistent urinary abnormalities in the presence of stable or improving renal function) by 3 months. This was associated with a rapid fall in ANCA titres, reduced inflammatory responses and improvements in renal function. At 12 months, three patients had repopulated B cells associated with the recurrence of circulating ANCAs, although no patients experienced major clinical relapse in the first 24 months. No unexpected side effects were observed. Conclusion. Treatment with ofatumumab resulted in similar serological and clinical responses to those seen in previous cohorts treated at our centre with a comparable CS, CYC and rituximab-based regimen. Ofatumumab should be considered an alternative B cell depleting agent in patients who are intolerant of, or unresponsive to, rituximab. Oxford University Press 2016-08 2016-04-19 /pmc/articles/PMC4957674/ /pubmed/27094598 http://dx.doi.org/10.1093/rheumatology/kew199 Text en © The Author 2016. Published by Oxford University Press on behalf of the British Society for Rheumatology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Science
McAdoo, Stephen P.
Bedi, Rachna
Tarzi, Ruth
Griffith, Megan
Pusey, Charles D.
Cairns, Thomas D.
Ofatumumab for B cell depletion therapy in ANCA-associated vasculitis: a single-centre case series
title Ofatumumab for B cell depletion therapy in ANCA-associated vasculitis: a single-centre case series
title_full Ofatumumab for B cell depletion therapy in ANCA-associated vasculitis: a single-centre case series
title_fullStr Ofatumumab for B cell depletion therapy in ANCA-associated vasculitis: a single-centre case series
title_full_unstemmed Ofatumumab for B cell depletion therapy in ANCA-associated vasculitis: a single-centre case series
title_short Ofatumumab for B cell depletion therapy in ANCA-associated vasculitis: a single-centre case series
title_sort ofatumumab for b cell depletion therapy in anca-associated vasculitis: a single-centre case series
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4957674/
https://www.ncbi.nlm.nih.gov/pubmed/27094598
http://dx.doi.org/10.1093/rheumatology/kew199
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