Literature DB >> 27288461

Should belatacept be the centrepiece of renal transplantation?

Monika Huber1, Stephan Kemmner1, Lutz Renders1, Uwe Heemann1.   

Abstract

Belatacept was developed to minimize cardiovascular risk and nephrotoxicity associated with calcineurin inhibitor (CNI)-based immunosuppression. Recently, 7-year data from the Belatacept Evaluation of Nephroprotection and Efficacy as First-line Immunosuppression Trial (BENEFIT), a phase III study comparing belatacept with cyclosporine, have been published. While during the first year of belatacept the risk of acute rejection episodes was elevated, this seemingly had marginal consequences for long-term graft survival and function as well as patient survival.For patients at a low-immunological risk, this drug seems to be a safe and effective alternative to CNI-based immunosuppression. Whether the higher rates of acute rejection episodes in the first year outweigh the gain in long-term graft function is still debated. In particular, the lower incidence of donor-specific antibodies indicates that belatacept should not be considered as lower intensity immunosuppression over the long term.Therefore, should belatacept be the centrepiece of immunosuppression for renal patients?All randomized trials so far have focussed on patients at a low immunological risk. Furthermore, cyclosporine A (CsA), the comparator of belatacept in BENEFIT and the Belatacept Evaluation of Nephroprotection and Efficacy as First-line Immunosuppression Trial-EXTended criteria donors (BENEFIT-EXT), is not the CNI of choice in modern transplantation. Furthermore, while at Year 7 the rate of cancer and infections was comparable with the CsA group, long-term data are missing on safety issues for a large number of patients. Thus, currently belatacept may be the drug of choice for a select group of patients, but not for everyone.This review highlights the benefits and uncertainties of the use of belatacept in kidney transplantation.
© The Author 2016. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved.

Entities:  

Keywords:  acute rejection; belatacept; co-stimulation blockade; kidney transplantation; side effects

Mesh:

Substances:

Year:  2016        PMID: 27288461     DOI: 10.1093/ndt/gfw226

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  3 in total

1.  Late conversion from tacrolimus to a belatacept-based immuno-suppression regime in kidney transplant recipients improves renal function, acid-base derangement and mineral-bone metabolism.

Authors:  Kevin Schulte; Clara Vollmer; Vera Klasen; Jan Hinrich Bräsen; Jodok Püchel; Christoph Borzikowsky; Ulrich Kunzendorf; Thorsten Feldkamp
Journal:  J Nephrol       Date:  2017-05-24       Impact factor: 3.902

Review 2.  Targeted Immunotherapy for Autoimmune Disease.

Authors:  Seung Min Jung; Wan-Uk Kim
Journal:  Immune Netw       Date:  2022-02-17       Impact factor: 5.851

Review 3.  Costimulation Blockade in Vascularized Composite Allotransplantation.

Authors:  Dimitrios Giannis; Dimitrios Moris; Linda C Cendales
Journal:  Front Immunol       Date:  2020-09-17       Impact factor: 7.561

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.