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Systematic conversion to generic tacrolimus in stable kidney transplant recipients
BACKGROUND: Tacrolimus (Prograf(®)) is a key drug in the immunosuppressive treatment of renal transplant patients. Since the expiration of the patent for Prograf(®), generic preparations have been approved in Europe as bioequivalence has been shown in healthy volunteers. However, few studies have in...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3970341/ https://www.ncbi.nlm.nih.gov/pubmed/24944783 http://dx.doi.org/10.1093/ckj/sfu015 |
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author | Rosenborg, Staffan Nordström, Annica Almquist, Tora Wennberg, Lars Bárány, Peter |
author_facet | Rosenborg, Staffan Nordström, Annica Almquist, Tora Wennberg, Lars Bárány, Peter |
author_sort | Rosenborg, Staffan |
collection | PubMed |
description | BACKGROUND: Tacrolimus (Prograf(®)) is a key drug in the immunosuppressive treatment of renal transplant patients. Since the expiration of the patent for Prograf(®), generic preparations have been approved in Europe as bioequivalence has been shown in healthy volunteers. However, few studies have investigated whether patients can be successfully converted from Prograf(®) to generic tacrolimus. Tacrolimus drug costs are by far the largest single item in the total drug expenditure for patients with renal disease in the Stockholm area. Considerable reductions in drug costs could be achieved if generic tacrolimus were to be used. The aim of this quality assurance study was to evaluate whether a switch from Prograf(®) to generic tacrolimus (Tacrolimus Sandoz(®)) could be safely performed in renal transplant patients. It further aimed to investigate changes of renal function (measured in estimated glomerular filtration rate, eGFR), need for dose changes and to calculate potential drug cost savings as a result of the conversion. METHODS: We planned to recruit at least 50 patients. Plasma creatinine levels and trough concentrations of tacrolimus were collected from patients with renal transplants at three occasions during treatment with Prograf(®) and three times after conversion to Tacrolimus Sandoz(®). The eGFR was calculated before and after the conversion. RESULTS: Sixty-three of 67 enrolled patients (69% males, age 28–80 years) are included in this analysis. The ratio of mean trough concentrations of tacrolimus after comparison with before conversion was 1.02 (90% confidence interval 0.95–1.09). Fourteen patients experienced a change in tacrolimus levels >20% compared with baseline, no patients changed >20% in eGFR. The drug cost saving per daily dose was 33.40 SEK (∼€3.60, −23%). CONCLUSIONS: Stable kidney transplant patients treated with Prograf(®) can be converted to Tacrolimus Sandoz(®) if trough concentrations of tacrolimus and plasma creatinine levels are closely monitored. The conversion brought savings, despite costs for extra monitoring. |
format | Online Article Text |
id | pubmed-3970341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39703412014-06-18 Systematic conversion to generic tacrolimus in stable kidney transplant recipients Rosenborg, Staffan Nordström, Annica Almquist, Tora Wennberg, Lars Bárány, Peter Clin Kidney J Original Contributions BACKGROUND: Tacrolimus (Prograf(®)) is a key drug in the immunosuppressive treatment of renal transplant patients. Since the expiration of the patent for Prograf(®), generic preparations have been approved in Europe as bioequivalence has been shown in healthy volunteers. However, few studies have investigated whether patients can be successfully converted from Prograf(®) to generic tacrolimus. Tacrolimus drug costs are by far the largest single item in the total drug expenditure for patients with renal disease in the Stockholm area. Considerable reductions in drug costs could be achieved if generic tacrolimus were to be used. The aim of this quality assurance study was to evaluate whether a switch from Prograf(®) to generic tacrolimus (Tacrolimus Sandoz(®)) could be safely performed in renal transplant patients. It further aimed to investigate changes of renal function (measured in estimated glomerular filtration rate, eGFR), need for dose changes and to calculate potential drug cost savings as a result of the conversion. METHODS: We planned to recruit at least 50 patients. Plasma creatinine levels and trough concentrations of tacrolimus were collected from patients with renal transplants at three occasions during treatment with Prograf(®) and three times after conversion to Tacrolimus Sandoz(®). The eGFR was calculated before and after the conversion. RESULTS: Sixty-three of 67 enrolled patients (69% males, age 28–80 years) are included in this analysis. The ratio of mean trough concentrations of tacrolimus after comparison with before conversion was 1.02 (90% confidence interval 0.95–1.09). Fourteen patients experienced a change in tacrolimus levels >20% compared with baseline, no patients changed >20% in eGFR. The drug cost saving per daily dose was 33.40 SEK (∼€3.60, −23%). CONCLUSIONS: Stable kidney transplant patients treated with Prograf(®) can be converted to Tacrolimus Sandoz(®) if trough concentrations of tacrolimus and plasma creatinine levels are closely monitored. The conversion brought savings, despite costs for extra monitoring. Oxford University Press 2014-04 2014-03-14 /pmc/articles/PMC3970341/ /pubmed/24944783 http://dx.doi.org/10.1093/ckj/sfu015 Text en © The Author 2014. Published by Oxford University Press on behalf of ERA-EDTA http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Contributions Rosenborg, Staffan Nordström, Annica Almquist, Tora Wennberg, Lars Bárány, Peter Systematic conversion to generic tacrolimus in stable kidney transplant recipients |
title | Systematic conversion to generic tacrolimus in stable kidney transplant recipients |
title_full | Systematic conversion to generic tacrolimus in stable kidney transplant recipients |
title_fullStr | Systematic conversion to generic tacrolimus in stable kidney transplant recipients |
title_full_unstemmed | Systematic conversion to generic tacrolimus in stable kidney transplant recipients |
title_short | Systematic conversion to generic tacrolimus in stable kidney transplant recipients |
title_sort | systematic conversion to generic tacrolimus in stable kidney transplant recipients |
topic | Original Contributions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3970341/ https://www.ncbi.nlm.nih.gov/pubmed/24944783 http://dx.doi.org/10.1093/ckj/sfu015 |
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