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Viral load-guided immunosuppression after lung transplantation (VIGILung)—study protocol for a randomized controlled trial
BACKGROUND: Immunosuppression including high-dose calcineurin inhibitors (CNI) is essential after lung transplantation. Dosing is usually guided by therapeutic drug monitoring adjusted to target trough levels of CNIs to keep the balance between over-dose causing severe toxicity and increased risk of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7798016/ https://www.ncbi.nlm.nih.gov/pubmed/33430927 http://dx.doi.org/10.1186/s13063-020-04985-w |
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author | Gottlieb, Jens Reuss, Alexander Mayer, Konstantin Weide, Karin Schade-Brittinger, Carmen Hoyer, Susanne Jaksch, Peter |
author_facet | Gottlieb, Jens Reuss, Alexander Mayer, Konstantin Weide, Karin Schade-Brittinger, Carmen Hoyer, Susanne Jaksch, Peter |
author_sort | Gottlieb, Jens |
collection | PubMed |
description | BACKGROUND: Immunosuppression including high-dose calcineurin inhibitors (CNI) is essential after lung transplantation. Dosing is usually guided by therapeutic drug monitoring adjusted to target trough levels of CNIs to keep the balance between over-dose causing severe toxicity and increased risk of infections or under-dose with a risk of graft injury. Adaptation of CNI-based immunosuppression by monitoring of torque teno virus (TTV), a latent nonpathogenic DNA virus, measured in the whole blood in addition to conventional therapeutic drug monitoring may reduce the toxicity of immunosuppression with similar efficacy. METHODS/DESIGN: An open-label, randomized, controlled, parallel-group, multicenter trial in lung transplant recipients will be conducted to investigate the safety and efficacy of immunosuppression guided by TTV monitoring as an add-on to conventional therapeutic drug monitoring. Adult lung transplant recipients 21 to 42 days after transplantation are eligible to participate. Patients (N = 144) will be randomized 1:1 to the experimental intervention (arm 1: immunosuppression guided by TTV monitoring in addition to conventional therapeutic drug monitoring of tacrolimus trough levels) and control intervention (arm 2: conventional therapeutic drug monitoring). Outcomes will be assessed 12 months after randomization with the change in glomerular filtration rate as the primary endpoint. Secondary endpoints will be additional measurements of renal function, allograft function, incidence of acute rejections, incidence of chronic lung allograft dysfunction, graft loss, and infections. DISCUSSION: The results of this randomized controlled trial may reduce the toxicity of immunosuppression after lung transplantation while maintaining the efficacy of immunosuppression. Study results are transferable to all other solid organ transplantations. TRIAL REGISTRATION: ClinicalTrials.gov NCT04198506. Registered on 12 December 2019 |
format | Online Article Text |
id | pubmed-7798016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77980162021-01-11 Viral load-guided immunosuppression after lung transplantation (VIGILung)—study protocol for a randomized controlled trial Gottlieb, Jens Reuss, Alexander Mayer, Konstantin Weide, Karin Schade-Brittinger, Carmen Hoyer, Susanne Jaksch, Peter Trials Study Protocol BACKGROUND: Immunosuppression including high-dose calcineurin inhibitors (CNI) is essential after lung transplantation. Dosing is usually guided by therapeutic drug monitoring adjusted to target trough levels of CNIs to keep the balance between over-dose causing severe toxicity and increased risk of infections or under-dose with a risk of graft injury. Adaptation of CNI-based immunosuppression by monitoring of torque teno virus (TTV), a latent nonpathogenic DNA virus, measured in the whole blood in addition to conventional therapeutic drug monitoring may reduce the toxicity of immunosuppression with similar efficacy. METHODS/DESIGN: An open-label, randomized, controlled, parallel-group, multicenter trial in lung transplant recipients will be conducted to investigate the safety and efficacy of immunosuppression guided by TTV monitoring as an add-on to conventional therapeutic drug monitoring. Adult lung transplant recipients 21 to 42 days after transplantation are eligible to participate. Patients (N = 144) will be randomized 1:1 to the experimental intervention (arm 1: immunosuppression guided by TTV monitoring in addition to conventional therapeutic drug monitoring of tacrolimus trough levels) and control intervention (arm 2: conventional therapeutic drug monitoring). Outcomes will be assessed 12 months after randomization with the change in glomerular filtration rate as the primary endpoint. Secondary endpoints will be additional measurements of renal function, allograft function, incidence of acute rejections, incidence of chronic lung allograft dysfunction, graft loss, and infections. DISCUSSION: The results of this randomized controlled trial may reduce the toxicity of immunosuppression after lung transplantation while maintaining the efficacy of immunosuppression. Study results are transferable to all other solid organ transplantations. TRIAL REGISTRATION: ClinicalTrials.gov NCT04198506. Registered on 12 December 2019 BioMed Central 2021-01-11 /pmc/articles/PMC7798016/ /pubmed/33430927 http://dx.doi.org/10.1186/s13063-020-04985-w Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Study Protocol Gottlieb, Jens Reuss, Alexander Mayer, Konstantin Weide, Karin Schade-Brittinger, Carmen Hoyer, Susanne Jaksch, Peter Viral load-guided immunosuppression after lung transplantation (VIGILung)—study protocol for a randomized controlled trial |
title | Viral load-guided immunosuppression after lung transplantation (VIGILung)—study protocol for a randomized controlled trial |
title_full | Viral load-guided immunosuppression after lung transplantation (VIGILung)—study protocol for a randomized controlled trial |
title_fullStr | Viral load-guided immunosuppression after lung transplantation (VIGILung)—study protocol for a randomized controlled trial |
title_full_unstemmed | Viral load-guided immunosuppression after lung transplantation (VIGILung)—study protocol for a randomized controlled trial |
title_short | Viral load-guided immunosuppression after lung transplantation (VIGILung)—study protocol for a randomized controlled trial |
title_sort | viral load-guided immunosuppression after lung transplantation (vigilung)—study protocol for a randomized controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7798016/ https://www.ncbi.nlm.nih.gov/pubmed/33430927 http://dx.doi.org/10.1186/s13063-020-04985-w |
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