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Belatacept for the prophylaxis of organ rejection in kidney transplant patients: an evidence-based review of its place in therapy

BACKGROUND: Belatacept is a novel immunosuppressive therapy designed to improve clinical outcomes associated with kidney transplant recipients while minimizing use of calcineurin inhibitors (CNIs). METHODS: We searched for clinical trials related to administration of belatacept to kidney transplant...

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Detalles Bibliográficos
Autores principales: Hardinger, Karen L, Sunderland, Daniel, Wiederrich, Jennifer A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4888760/
https://www.ncbi.nlm.nih.gov/pubmed/27307759
http://dx.doi.org/10.2147/IJNRD.S88816
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author Hardinger, Karen L
Sunderland, Daniel
Wiederrich, Jennifer A
author_facet Hardinger, Karen L
Sunderland, Daniel
Wiederrich, Jennifer A
author_sort Hardinger, Karen L
collection PubMed
description BACKGROUND: Belatacept is a novel immunosuppressive therapy designed to improve clinical outcomes associated with kidney transplant recipients while minimizing use of calcineurin inhibitors (CNIs). METHODS: We searched for clinical trials related to administration of belatacept to kidney transplant patients compared to various immunosuppression regimens, as well as for studies that utilized data from belatacept trials to validate new surrogate measures. The purpose of this review is to consolidate the published evidence of belatacept’s effectiveness and safety in renal transplant recipients to better elucidate its place in clinical practice. RESULTS: Analysis of the results from the Belatacept Evaluation of Nephroprotection and Effi-cacy as First-Line Immunosuppressive Trial (BENEFIT) study, a de novo trial that compared cyclosporine (CsA)-based therapy to belatacept-based therapy in standard criteria donors, found a significant difference in mean estimated glomerular filtration rate (eGFR) of 13–15 mL/min/1.73 m(2) and 23–27 mL/min/1.73 m(2) at 1 year and 7 years, respectively. The BENEFIT-EXT study was similarly designed with the exception that it included extended criteria donors. Renal function improved significantly for the more intensive belatacept group in all years of the BENEFIT-EXT study; however, it was not significant in the less intensive group until 5 years after transplant. Belatacept regimens resulted in lower blood pressure, cholesterol levels, and incidence of new-onset diabetes after transplant compared to CsA-based regimens. Results from conversion of CNIs to belatacept therapy, dual therapy of belatacept with sirolimus, and belatacept with corticosteroid avoidance therapy are also included in this article. CONCLUSION: The evidence reviewed in this article suggests that belatacept is an effective alternative in kidney transplant recipients. Compared to CNI-based therapy, belatacept-based therapy results in superior renal function and similar rates of allograft survival. In terms of safety, belatacept was shown to have lower incidence of hypertension, hyperlipidemia, and diabetes; however, incidence of posttransplantation lymphoproliferative disorder and the cost of belatacept may hinder use of this medication.
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spelling pubmed-48887602016-06-15 Belatacept for the prophylaxis of organ rejection in kidney transplant patients: an evidence-based review of its place in therapy Hardinger, Karen L Sunderland, Daniel Wiederrich, Jennifer A Int J Nephrol Renovasc Dis Review BACKGROUND: Belatacept is a novel immunosuppressive therapy designed to improve clinical outcomes associated with kidney transplant recipients while minimizing use of calcineurin inhibitors (CNIs). METHODS: We searched for clinical trials related to administration of belatacept to kidney transplant patients compared to various immunosuppression regimens, as well as for studies that utilized data from belatacept trials to validate new surrogate measures. The purpose of this review is to consolidate the published evidence of belatacept’s effectiveness and safety in renal transplant recipients to better elucidate its place in clinical practice. RESULTS: Analysis of the results from the Belatacept Evaluation of Nephroprotection and Effi-cacy as First-Line Immunosuppressive Trial (BENEFIT) study, a de novo trial that compared cyclosporine (CsA)-based therapy to belatacept-based therapy in standard criteria donors, found a significant difference in mean estimated glomerular filtration rate (eGFR) of 13–15 mL/min/1.73 m(2) and 23–27 mL/min/1.73 m(2) at 1 year and 7 years, respectively. The BENEFIT-EXT study was similarly designed with the exception that it included extended criteria donors. Renal function improved significantly for the more intensive belatacept group in all years of the BENEFIT-EXT study; however, it was not significant in the less intensive group until 5 years after transplant. Belatacept regimens resulted in lower blood pressure, cholesterol levels, and incidence of new-onset diabetes after transplant compared to CsA-based regimens. Results from conversion of CNIs to belatacept therapy, dual therapy of belatacept with sirolimus, and belatacept with corticosteroid avoidance therapy are also included in this article. CONCLUSION: The evidence reviewed in this article suggests that belatacept is an effective alternative in kidney transplant recipients. Compared to CNI-based therapy, belatacept-based therapy results in superior renal function and similar rates of allograft survival. In terms of safety, belatacept was shown to have lower incidence of hypertension, hyperlipidemia, and diabetes; however, incidence of posttransplantation lymphoproliferative disorder and the cost of belatacept may hinder use of this medication. Dove Medical Press 2016-05-26 /pmc/articles/PMC4888760/ /pubmed/27307759 http://dx.doi.org/10.2147/IJNRD.S88816 Text en © 2016 Hardinger et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Hardinger, Karen L
Sunderland, Daniel
Wiederrich, Jennifer A
Belatacept for the prophylaxis of organ rejection in kidney transplant patients: an evidence-based review of its place in therapy
title Belatacept for the prophylaxis of organ rejection in kidney transplant patients: an evidence-based review of its place in therapy
title_full Belatacept for the prophylaxis of organ rejection in kidney transplant patients: an evidence-based review of its place in therapy
title_fullStr Belatacept for the prophylaxis of organ rejection in kidney transplant patients: an evidence-based review of its place in therapy
title_full_unstemmed Belatacept for the prophylaxis of organ rejection in kidney transplant patients: an evidence-based review of its place in therapy
title_short Belatacept for the prophylaxis of organ rejection in kidney transplant patients: an evidence-based review of its place in therapy
title_sort belatacept for the prophylaxis of organ rejection in kidney transplant patients: an evidence-based review of its place in therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4888760/
https://www.ncbi.nlm.nih.gov/pubmed/27307759
http://dx.doi.org/10.2147/IJNRD.S88816
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