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Campath, calcineurin inhibitor reduction and chronic allograft nephropathy (3C) study: background, rationale, and study protocol

BACKGROUND: Kidney transplantation is the best treatment for patients with end-stage renal failure, but uncertainty remains about the best immunosuppression strategy. Long-term graft survival has not improved substantially, and one possible explanation is calcineurin inhibitor (CNI) nephrotoxicity....

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Autores principales: Haynes, Richard, Baigent, Colin, Harden, Paul, Landray, Martin, Akyol, Murat, Asderakis, Argiris, Baxter, Alex, Bhandari, Sunil, Chowdhury, Paramit, Clancy, Marc, Emberson, Jonathan, Gibbs, Paul, Hammad, Abdul, Herrington, Will, Jayne, Kathy, Jones, Gareth, Krishnan, Nithya, Lay, Michael, Lewis, David, Macdougall, Iain, Nathan, Chidambaram, Neuberger, James, Newstead, Chas, Pararajasingam, Ravi, Puliatti, Carmelo, Rigg, Keith, Rowe, Peter, Sharif, Adnan, Sheerin, Neil, Sinha, Sanjay, Watson, Chris, Friend, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674985/
https://www.ncbi.nlm.nih.gov/pubmed/23641902
http://dx.doi.org/10.1186/2047-1440-2-7
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author Haynes, Richard
Baigent, Colin
Harden, Paul
Landray, Martin
Akyol, Murat
Asderakis, Argiris
Baxter, Alex
Bhandari, Sunil
Chowdhury, Paramit
Clancy, Marc
Emberson, Jonathan
Gibbs, Paul
Hammad, Abdul
Herrington, Will
Jayne, Kathy
Jones, Gareth
Krishnan, Nithya
Lay, Michael
Lewis, David
Macdougall, Iain
Nathan, Chidambaram
Neuberger, James
Newstead, Chas
Pararajasingam, Ravi
Puliatti, Carmelo
Rigg, Keith
Rowe, Peter
Sharif, Adnan
Sheerin, Neil
Sinha, Sanjay
Watson, Chris
Friend, Peter
author_facet Haynes, Richard
Baigent, Colin
Harden, Paul
Landray, Martin
Akyol, Murat
Asderakis, Argiris
Baxter, Alex
Bhandari, Sunil
Chowdhury, Paramit
Clancy, Marc
Emberson, Jonathan
Gibbs, Paul
Hammad, Abdul
Herrington, Will
Jayne, Kathy
Jones, Gareth
Krishnan, Nithya
Lay, Michael
Lewis, David
Macdougall, Iain
Nathan, Chidambaram
Neuberger, James
Newstead, Chas
Pararajasingam, Ravi
Puliatti, Carmelo
Rigg, Keith
Rowe, Peter
Sharif, Adnan
Sheerin, Neil
Sinha, Sanjay
Watson, Chris
Friend, Peter
author_sort Haynes, Richard
collection PubMed
description BACKGROUND: Kidney transplantation is the best treatment for patients with end-stage renal failure, but uncertainty remains about the best immunosuppression strategy. Long-term graft survival has not improved substantially, and one possible explanation is calcineurin inhibitor (CNI) nephrotoxicity. CNI exposure could be minimized by using more potent induction therapy or alternative maintenance therapy to remove CNIs completely. However, the safety and efficacy of such strategies are unknown. METHODS/DESIGN: The Campath, Calcineurin inhibitor reduction and Chronic allograft nephropathy (3C) Study is a multicentre, open-label, randomized controlled trial with 852 participants which is addressing two important questions in kidney transplantation. The first question is whether a Campath (alemtuzumab)-based induction therapy strategy is superior to basiliximab-based therapy, and the second is whether, from 6 months after transplantation, a sirolimus-based maintenance therapy strategy is superior to tacrolimus-based therapy. Recruitment is complete, and follow-up will continue for around 5 years post-transplant. The primary endpoint for the induction therapy comparison is biopsy-proven acute rejection by 6 months, and the primary endpoint for the maintenance therapy comparison is change in estimated glomerular filtration rate from baseline to 2 years after transplantation. The study is sponsored by the University of Oxford and endorsed by the British Transplantation Society, and 18 centers for adult kidney transplant are participating. DISCUSSION: Late graft failure is a major issue for kidney-transplant recipients. If our hypothesis that minimizing CNI exposure with Campath-based induction therapy and/or an elective conversion to sirolimus-based maintenance therapy can improve long-term graft function and survival is correct, then patients should experience better graft function for longer. A positive outcome could change clinical practice in kidney transplantation. TRIAL REGISTRATION: ClinicalTrials.gov, NCT01120028 and ISRCTN88894088
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spelling pubmed-36749852013-06-10 Campath, calcineurin inhibitor reduction and chronic allograft nephropathy (3C) study: background, rationale, and study protocol Haynes, Richard Baigent, Colin Harden, Paul Landray, Martin Akyol, Murat Asderakis, Argiris Baxter, Alex Bhandari, Sunil Chowdhury, Paramit Clancy, Marc Emberson, Jonathan Gibbs, Paul Hammad, Abdul Herrington, Will Jayne, Kathy Jones, Gareth Krishnan, Nithya Lay, Michael Lewis, David Macdougall, Iain Nathan, Chidambaram Neuberger, James Newstead, Chas Pararajasingam, Ravi Puliatti, Carmelo Rigg, Keith Rowe, Peter Sharif, Adnan Sheerin, Neil Sinha, Sanjay Watson, Chris Friend, Peter Transplant Res Clinical Trial Protocol BACKGROUND: Kidney transplantation is the best treatment for patients with end-stage renal failure, but uncertainty remains about the best immunosuppression strategy. Long-term graft survival has not improved substantially, and one possible explanation is calcineurin inhibitor (CNI) nephrotoxicity. CNI exposure could be minimized by using more potent induction therapy or alternative maintenance therapy to remove CNIs completely. However, the safety and efficacy of such strategies are unknown. METHODS/DESIGN: The Campath, Calcineurin inhibitor reduction and Chronic allograft nephropathy (3C) Study is a multicentre, open-label, randomized controlled trial with 852 participants which is addressing two important questions in kidney transplantation. The first question is whether a Campath (alemtuzumab)-based induction therapy strategy is superior to basiliximab-based therapy, and the second is whether, from 6 months after transplantation, a sirolimus-based maintenance therapy strategy is superior to tacrolimus-based therapy. Recruitment is complete, and follow-up will continue for around 5 years post-transplant. The primary endpoint for the induction therapy comparison is biopsy-proven acute rejection by 6 months, and the primary endpoint for the maintenance therapy comparison is change in estimated glomerular filtration rate from baseline to 2 years after transplantation. The study is sponsored by the University of Oxford and endorsed by the British Transplantation Society, and 18 centers for adult kidney transplant are participating. DISCUSSION: Late graft failure is a major issue for kidney-transplant recipients. If our hypothesis that minimizing CNI exposure with Campath-based induction therapy and/or an elective conversion to sirolimus-based maintenance therapy can improve long-term graft function and survival is correct, then patients should experience better graft function for longer. A positive outcome could change clinical practice in kidney transplantation. TRIAL REGISTRATION: ClinicalTrials.gov, NCT01120028 and ISRCTN88894088 BioMed Central 2013-05-06 /pmc/articles/PMC3674985/ /pubmed/23641902 http://dx.doi.org/10.1186/2047-1440-2-7 Text en Copyright © 2013 Haynes et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Trial Protocol
Haynes, Richard
Baigent, Colin
Harden, Paul
Landray, Martin
Akyol, Murat
Asderakis, Argiris
Baxter, Alex
Bhandari, Sunil
Chowdhury, Paramit
Clancy, Marc
Emberson, Jonathan
Gibbs, Paul
Hammad, Abdul
Herrington, Will
Jayne, Kathy
Jones, Gareth
Krishnan, Nithya
Lay, Michael
Lewis, David
Macdougall, Iain
Nathan, Chidambaram
Neuberger, James
Newstead, Chas
Pararajasingam, Ravi
Puliatti, Carmelo
Rigg, Keith
Rowe, Peter
Sharif, Adnan
Sheerin, Neil
Sinha, Sanjay
Watson, Chris
Friend, Peter
Campath, calcineurin inhibitor reduction and chronic allograft nephropathy (3C) study: background, rationale, and study protocol
title Campath, calcineurin inhibitor reduction and chronic allograft nephropathy (3C) study: background, rationale, and study protocol
title_full Campath, calcineurin inhibitor reduction and chronic allograft nephropathy (3C) study: background, rationale, and study protocol
title_fullStr Campath, calcineurin inhibitor reduction and chronic allograft nephropathy (3C) study: background, rationale, and study protocol
title_full_unstemmed Campath, calcineurin inhibitor reduction and chronic allograft nephropathy (3C) study: background, rationale, and study protocol
title_short Campath, calcineurin inhibitor reduction and chronic allograft nephropathy (3C) study: background, rationale, and study protocol
title_sort campath, calcineurin inhibitor reduction and chronic allograft nephropathy (3c) study: background, rationale, and study protocol
topic Clinical Trial Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674985/
https://www.ncbi.nlm.nih.gov/pubmed/23641902
http://dx.doi.org/10.1186/2047-1440-2-7
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