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Tocilizumab in the treatment of twelve cases with aa amyloidosis secondary to familial mediterranean fever

BACKGROUND: There is no established treatment of AA amyloidosis, a long-term complication of various chronic inflammatory diseases associated with increased mortality, such as familial Mediterranian fever (FMF). Recently there are few reports pointing out that tocilizumab(TCZ), an anti IL-6 agent ma...

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Autores principales: Ugurlu, Serdal, Hacioglu, Aysa, Adibnia, Yasaman, Hamuryudan, Vedat, Ozdogan, Huri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5450086/
https://www.ncbi.nlm.nih.gov/pubmed/28558744
http://dx.doi.org/10.1186/s13023-017-0642-0
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author Ugurlu, Serdal
Hacioglu, Aysa
Adibnia, Yasaman
Hamuryudan, Vedat
Ozdogan, Huri
author_facet Ugurlu, Serdal
Hacioglu, Aysa
Adibnia, Yasaman
Hamuryudan, Vedat
Ozdogan, Huri
author_sort Ugurlu, Serdal
collection PubMed
description BACKGROUND: There is no established treatment of AA amyloidosis, a long-term complication of various chronic inflammatory diseases associated with increased mortality, such as familial Mediterranian fever (FMF). Recently there are few reports pointing out that tocilizumab(TCZ), an anti IL-6 agent may be effective in AA amyloidosis resistant to conventional treatments. We report our data on the effect of TCZ in patients with FMF complicated with AA amyloidosis. METHODS: FMF patients with histologically proven AA amyloidosis, treated with TCZ (8 mg/kg per month) were followed monthly and the changes in creatinine, creatinine clearance, the amount of 24-hour urinary protein, erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) were noted throughout the treatment period. Adverse effects of the treatment were closely monitored. RESULTS: TCZ was given to 12 patients (6 F, 6 M) who also continued to receive colchicine (1.9 ± 0.4 mg/day). Coexisting diseases were ankylosing spondylitis(4) and Crohn’s disease(1). The mean age was 35.2 ± 10.0 years and the mean follow-up on TCZ was 17.5 ± 14.7 months. The renal functions remained stable (mean creatinine from 1.1 ± 0.9 mg/dl to 1.0 ± 0.6 mg/dl), while a significant decrease in acute phase response (the mean CRP from 18.1 ± 19.5 mg/L to 5.8 ± 7.1 mg/L and ESR from 48.7 ± 31.0 mm/h to 28.7 ± 28.3 mm/h) was observed and the mean 24-hour urinary protein excretion reduced from 6537.6 ± 6526.0 mg/dl to 4745.5 ± 5462.7 mg/dl. Two patients whose renal functions were impaired prior to TCZ therapy improved significantly on this regimen. No infusion reaction was observed. None of the patients experienced any FMF attack under TCZ treatment with the exception of 2, one of whom had less frequent attacks while the other had episodes of erysipelas-like erythema. CONCLUSİON: Tocilizumab improved the acute phase response and the renal function in this group of patients and was generally well tolerated. Besides improving the renal function TCZ seemed to control the recurrence of FMF attacks too. Further studies are warrented to test the efficacy and safety of TCZ in AA amyloidosis secondary to FMF as well as other inflammatory conditions.
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spelling pubmed-54500862017-06-01 Tocilizumab in the treatment of twelve cases with aa amyloidosis secondary to familial mediterranean fever Ugurlu, Serdal Hacioglu, Aysa Adibnia, Yasaman Hamuryudan, Vedat Ozdogan, Huri Orphanet J Rare Dis Research BACKGROUND: There is no established treatment of AA amyloidosis, a long-term complication of various chronic inflammatory diseases associated with increased mortality, such as familial Mediterranian fever (FMF). Recently there are few reports pointing out that tocilizumab(TCZ), an anti IL-6 agent may be effective in AA amyloidosis resistant to conventional treatments. We report our data on the effect of TCZ in patients with FMF complicated with AA amyloidosis. METHODS: FMF patients with histologically proven AA amyloidosis, treated with TCZ (8 mg/kg per month) were followed monthly and the changes in creatinine, creatinine clearance, the amount of 24-hour urinary protein, erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) were noted throughout the treatment period. Adverse effects of the treatment were closely monitored. RESULTS: TCZ was given to 12 patients (6 F, 6 M) who also continued to receive colchicine (1.9 ± 0.4 mg/day). Coexisting diseases were ankylosing spondylitis(4) and Crohn’s disease(1). The mean age was 35.2 ± 10.0 years and the mean follow-up on TCZ was 17.5 ± 14.7 months. The renal functions remained stable (mean creatinine from 1.1 ± 0.9 mg/dl to 1.0 ± 0.6 mg/dl), while a significant decrease in acute phase response (the mean CRP from 18.1 ± 19.5 mg/L to 5.8 ± 7.1 mg/L and ESR from 48.7 ± 31.0 mm/h to 28.7 ± 28.3 mm/h) was observed and the mean 24-hour urinary protein excretion reduced from 6537.6 ± 6526.0 mg/dl to 4745.5 ± 5462.7 mg/dl. Two patients whose renal functions were impaired prior to TCZ therapy improved significantly on this regimen. No infusion reaction was observed. None of the patients experienced any FMF attack under TCZ treatment with the exception of 2, one of whom had less frequent attacks while the other had episodes of erysipelas-like erythema. CONCLUSİON: Tocilizumab improved the acute phase response and the renal function in this group of patients and was generally well tolerated. Besides improving the renal function TCZ seemed to control the recurrence of FMF attacks too. Further studies are warrented to test the efficacy and safety of TCZ in AA amyloidosis secondary to FMF as well as other inflammatory conditions. BioMed Central 2017-05-30 /pmc/articles/PMC5450086/ /pubmed/28558744 http://dx.doi.org/10.1186/s13023-017-0642-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Ugurlu, Serdal
Hacioglu, Aysa
Adibnia, Yasaman
Hamuryudan, Vedat
Ozdogan, Huri
Tocilizumab in the treatment of twelve cases with aa amyloidosis secondary to familial mediterranean fever
title Tocilizumab in the treatment of twelve cases with aa amyloidosis secondary to familial mediterranean fever
title_full Tocilizumab in the treatment of twelve cases with aa amyloidosis secondary to familial mediterranean fever
title_fullStr Tocilizumab in the treatment of twelve cases with aa amyloidosis secondary to familial mediterranean fever
title_full_unstemmed Tocilizumab in the treatment of twelve cases with aa amyloidosis secondary to familial mediterranean fever
title_short Tocilizumab in the treatment of twelve cases with aa amyloidosis secondary to familial mediterranean fever
title_sort tocilizumab in the treatment of twelve cases with aa amyloidosis secondary to familial mediterranean fever
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5450086/
https://www.ncbi.nlm.nih.gov/pubmed/28558744
http://dx.doi.org/10.1186/s13023-017-0642-0
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