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Calcineurin inhibitors in systemic sclerosis – a systematic literature review

OBJECTIVE: To review treatment effectiveness and adverse events of calcineurin inhibitors (CNIs) such as cyclosporin A (CsA) and tacrolimus in patients with systemic sclerosis (SSc). METHODS: A systematic literature search was performed on PubMed and Web of Science using the predefined keywords ‘sys...

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Autores principales: Hofmann, Nina N., Ambühl, Robert A., Jordan, Suzana, Distler, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127851/
https://www.ncbi.nlm.nih.gov/pubmed/35619877
http://dx.doi.org/10.1177/1759720X221092374
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author Hofmann, Nina N.
Ambühl, Robert A.
Jordan, Suzana
Distler, Oliver
author_facet Hofmann, Nina N.
Ambühl, Robert A.
Jordan, Suzana
Distler, Oliver
author_sort Hofmann, Nina N.
collection PubMed
description OBJECTIVE: To review treatment effectiveness and adverse events of calcineurin inhibitors (CNIs) such as cyclosporin A (CsA) and tacrolimus in patients with systemic sclerosis (SSc). METHODS: A systematic literature search was performed on PubMed and Web of Science using the predefined keywords ‘systemic sclerosis’, scleroderma, cyclosporin*, and tacrolimus. Articles were eligible for inclusion, if SSc patients had been treated with CNIs and data on treatment effects were available. RESULTS: This systematic literature review identified 37 papers (19 case reports, 15 case series, 2 controlled studies, and 1 retrospective study) including 134 SSc patients treated with CNIs. In 34 of 37 papers, CsA was used. An improvement of skin fibrosis was observed in 77 of 96 (80.2%) patients using a wide variety of outcome measures and dose regimes. Both controlled studies showed significant improvements, one using a historical control group and one using a no-treatment control group. Improvement in pulmonary function tests (PFTs) occurred in 67.9% (19/28) of the patients who had reduced PFTs at baseline. In 58 (43.3%) cases, adverse renal events were reported, of which 7 (5.2%) were severe such as scleroderma renal crisis (SRC), CsA-associated nephropathy, or death by renal insufficiency. Adverse events led to dose reduction, treatment interruption, or withdrawal in 39 of 134 (29.1%). CONCLUSION: In this systematic literature review, signals for potential effectiveness of CsA for skin and pulmonary fibrosis were found, but the evidence level of the identified studies was too low to allow robust conclusions. Randomized controlled double-blind trials are needed to conclude on the effectiveness of CNIs in SSc. Renal toxicity of CNIs was confirmed in this review and needs to be considered in the design of such studies.
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spelling pubmed-91278512022-05-25 Calcineurin inhibitors in systemic sclerosis – a systematic literature review Hofmann, Nina N. Ambühl, Robert A. Jordan, Suzana Distler, Oliver Ther Adv Musculoskelet Dis Systematic Review OBJECTIVE: To review treatment effectiveness and adverse events of calcineurin inhibitors (CNIs) such as cyclosporin A (CsA) and tacrolimus in patients with systemic sclerosis (SSc). METHODS: A systematic literature search was performed on PubMed and Web of Science using the predefined keywords ‘systemic sclerosis’, scleroderma, cyclosporin*, and tacrolimus. Articles were eligible for inclusion, if SSc patients had been treated with CNIs and data on treatment effects were available. RESULTS: This systematic literature review identified 37 papers (19 case reports, 15 case series, 2 controlled studies, and 1 retrospective study) including 134 SSc patients treated with CNIs. In 34 of 37 papers, CsA was used. An improvement of skin fibrosis was observed in 77 of 96 (80.2%) patients using a wide variety of outcome measures and dose regimes. Both controlled studies showed significant improvements, one using a historical control group and one using a no-treatment control group. Improvement in pulmonary function tests (PFTs) occurred in 67.9% (19/28) of the patients who had reduced PFTs at baseline. In 58 (43.3%) cases, adverse renal events were reported, of which 7 (5.2%) were severe such as scleroderma renal crisis (SRC), CsA-associated nephropathy, or death by renal insufficiency. Adverse events led to dose reduction, treatment interruption, or withdrawal in 39 of 134 (29.1%). CONCLUSION: In this systematic literature review, signals for potential effectiveness of CsA for skin and pulmonary fibrosis were found, but the evidence level of the identified studies was too low to allow robust conclusions. Randomized controlled double-blind trials are needed to conclude on the effectiveness of CNIs in SSc. Renal toxicity of CNIs was confirmed in this review and needs to be considered in the design of such studies. SAGE Publications 2022-05-19 /pmc/articles/PMC9127851/ /pubmed/35619877 http://dx.doi.org/10.1177/1759720X221092374 Text en © The Author(s), 2022 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Systematic Review
Hofmann, Nina N.
Ambühl, Robert A.
Jordan, Suzana
Distler, Oliver
Calcineurin inhibitors in systemic sclerosis – a systematic literature review
title Calcineurin inhibitors in systemic sclerosis – a systematic literature review
title_full Calcineurin inhibitors in systemic sclerosis – a systematic literature review
title_fullStr Calcineurin inhibitors in systemic sclerosis – a systematic literature review
title_full_unstemmed Calcineurin inhibitors in systemic sclerosis – a systematic literature review
title_short Calcineurin inhibitors in systemic sclerosis – a systematic literature review
title_sort calcineurin inhibitors in systemic sclerosis – a systematic literature review
topic Systematic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127851/
https://www.ncbi.nlm.nih.gov/pubmed/35619877
http://dx.doi.org/10.1177/1759720X221092374
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