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Retreatment with Pegloticase after a Gap in Therapy in Patients with Gout: A Report of Four Cases

INTRODUCTION: Pegloticase, a potent uricolytic biologic enzyme, has been shown to be an effective therapeutic option in patients with uncontrolled gout. However, there are limited data on clinical response after a gap in therapy and retreatment with pegloticase. CASE SERIES: This report describes fo...

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Autores principales: Morton, Allan H., Hosey, Tony, LaMoreaux, Brian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251856/
https://www.ncbi.nlm.nih.gov/pubmed/29725991
http://dx.doi.org/10.1007/s40744-018-0111-9
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author Morton, Allan H.
Hosey, Tony
LaMoreaux, Brian
author_facet Morton, Allan H.
Hosey, Tony
LaMoreaux, Brian
author_sort Morton, Allan H.
collection PubMed
description INTRODUCTION: Pegloticase, a potent uricolytic biologic enzyme, has been shown to be an effective therapeutic option in patients with uncontrolled gout. However, there are limited data on clinical response after a gap in therapy and retreatment with pegloticase. CASE SERIES: This report describes four patients with chronic gout who were successfully managed with pegloticase and were retreated following a gap in therapy. Patient charts from a practice-based rheumatology clinic were retrospectively analyzed; four male patients, aged 70–75 years, with chronic gout and a more than 4-week gap in pegloticase therapy were reviewed. Before pegloticase treatment, patients had received allopurinol or febuxostat, but they continued exhibiting symptoms, including visible tophi and serum uric acid (SUA) levels of 5.2–10.2 mg/dL (309–607 μmol/L), despite oral urate-lowering therapy. The first pegloticase treatment (8-mg infusion every 2 weeks) lasted 22–124 weeks. Pegloticase resolved tophi and improved SUA to below 1.5 mg/dL (less than 89 μmol/L); however, patients discontinued pegloticase because of symptom resolution, poor adherence, or personal reasons. Following treatment gaps (12–156 weeks), symptoms and SUA levels increased and patients were retreated with pegloticase (4–147 weeks). In three of four patients, reinitiating pegloticase lowered SUA levels to below 1.0 mg/dL (less than 59 μmol/L) and resolved symptoms. One patient experienced an infusion reaction and discontinued; no infusion reactions, gout flares, or adverse events occurred among the other three patients. CONCLUSION: Retreatment with pegloticase after a gap in therapy appears to be an effective and tolerated option in prior responders. FUNDING: Horizon Pharma.
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spelling pubmed-62518562018-12-10 Retreatment with Pegloticase after a Gap in Therapy in Patients with Gout: A Report of Four Cases Morton, Allan H. Hosey, Tony LaMoreaux, Brian Rheumatol Ther Case Series INTRODUCTION: Pegloticase, a potent uricolytic biologic enzyme, has been shown to be an effective therapeutic option in patients with uncontrolled gout. However, there are limited data on clinical response after a gap in therapy and retreatment with pegloticase. CASE SERIES: This report describes four patients with chronic gout who were successfully managed with pegloticase and were retreated following a gap in therapy. Patient charts from a practice-based rheumatology clinic were retrospectively analyzed; four male patients, aged 70–75 years, with chronic gout and a more than 4-week gap in pegloticase therapy were reviewed. Before pegloticase treatment, patients had received allopurinol or febuxostat, but they continued exhibiting symptoms, including visible tophi and serum uric acid (SUA) levels of 5.2–10.2 mg/dL (309–607 μmol/L), despite oral urate-lowering therapy. The first pegloticase treatment (8-mg infusion every 2 weeks) lasted 22–124 weeks. Pegloticase resolved tophi and improved SUA to below 1.5 mg/dL (less than 89 μmol/L); however, patients discontinued pegloticase because of symptom resolution, poor adherence, or personal reasons. Following treatment gaps (12–156 weeks), symptoms and SUA levels increased and patients were retreated with pegloticase (4–147 weeks). In three of four patients, reinitiating pegloticase lowered SUA levels to below 1.0 mg/dL (less than 59 μmol/L) and resolved symptoms. One patient experienced an infusion reaction and discontinued; no infusion reactions, gout flares, or adverse events occurred among the other three patients. CONCLUSION: Retreatment with pegloticase after a gap in therapy appears to be an effective and tolerated option in prior responders. FUNDING: Horizon Pharma. Springer Healthcare 2018-05-03 /pmc/articles/PMC6251856/ /pubmed/29725991 http://dx.doi.org/10.1007/s40744-018-0111-9 Text en © The Author(s) 2018 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Case Series
Morton, Allan H.
Hosey, Tony
LaMoreaux, Brian
Retreatment with Pegloticase after a Gap in Therapy in Patients with Gout: A Report of Four Cases
title Retreatment with Pegloticase after a Gap in Therapy in Patients with Gout: A Report of Four Cases
title_full Retreatment with Pegloticase after a Gap in Therapy in Patients with Gout: A Report of Four Cases
title_fullStr Retreatment with Pegloticase after a Gap in Therapy in Patients with Gout: A Report of Four Cases
title_full_unstemmed Retreatment with Pegloticase after a Gap in Therapy in Patients with Gout: A Report of Four Cases
title_short Retreatment with Pegloticase after a Gap in Therapy in Patients with Gout: A Report of Four Cases
title_sort retreatment with pegloticase after a gap in therapy in patients with gout: a report of four cases
topic Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251856/
https://www.ncbi.nlm.nih.gov/pubmed/29725991
http://dx.doi.org/10.1007/s40744-018-0111-9
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