Literature DB >> 23909498

Induction therapy and mTOR inhibition: minimizing calcineurin inhibitor exposure in de novo renal transplant patients.

Björn Nashan1.   

Abstract

Use of induction therapy with mTOR inhibitor maintenance immunosuppression to facilitate reduced calcineurin inhibitor (CNI) exposure in de novo kidney transplant patients has been explored in a series of randomized trials. These studies have typically employed interleukin-2 receptor antagonist (IL-2RA) induction, in low or standard immunological risk recipients. Although no study has directly compared mTOR inhibition plus reduced CNI exposure with or without induction, inclusion of IL-2RA induction appears to permit a substantial reduction in CNI exposure without the need for high mTOR inhibitor dosing. IL-2RA induction with an mTOR inhibitor and steroids has consistently shown similar efficacy to standard-exposure CNI with mycophenolic acid and steroids and may improve renal function among patients who remain on the mTOR inhibitor-based regimen. With modern mTOR inhibitor dosing, wound healing complications are of less concern and may be no more frequent than in mycophenolic acid-based regimens. The incidence of cytomegalovirus infection appears lower in patients receiving de novo mTOR inhibition. The available evidence demonstrates that IL-2RA induction with an mTOR inhibitor can successfully reduce CNI exposure by at least half without a penalty in terms of rejection in low- or moderate-risk de novo transplant recipients and may offer renal and antiviral benefits.
© 2013 John Wiley & Sons A/S.

Entities:  

Keywords:  antithymocyte globulin; basiliximab; calcineurin inhibitors; daclizumab; everolimus; induction; kidney transplantation; mTOR inhibitors; minimization; sirolimus

Mesh:

Substances:

Year:  2013        PMID: 23909498     DOI: 10.1111/ctr.12156

Source DB:  PubMed          Journal:  Clin Transplant        ISSN: 0902-0063            Impact factor:   2.863


  6 in total

1.  Evaluating the efficacy, safety and evolution of renal function with early initiation of everolimus-facilitated tacrolimus reduction in de novo liver transplant recipients: Study protocol for a randomized controlled trial.

Authors:  Bjorn Nashan; Peter Schemmer; Felix Braun; Markus Dworak; Peter Wimmer; Hans Schlitt
Journal:  Trials       Date:  2015-03-26       Impact factor: 2.279

2.  Host cell mTORC1 is required for HCV RNA replication.

Authors:  Stefanie Stöhr; Rui Costa; Lisa Sandmann; Sandra Westhaus; Stephanie Pfaender; Eva Dazert; Philip Meuleman; Florian W R Vondran; Michael P Manns; Eike Steinmann; Thomas von Hahn; Sandra Ciesek
Journal:  Gut       Date:  2015-08-14       Impact factor: 23.059

Review 3.  Is Early Conversion to mTOR Inhibitors Represent a Suitable Choice in Renal Transplant Recipients? A Systemic Review of Medium-term Outcomes.

Authors:  J Kumar; I Reccia; T Kusano
Journal:  Int J Organ Transplant Med       Date:  2017-05-01

4.  Systemic meta-analysis assessing the short term applicability of early conversion to mammalian target of rapamycin inhibitors in kidney transplant.

Authors:  Jayant Kumar; Isabella Reccia; Tomokazu Kusano; Bridson M Julie; Ajay Sharma; Ahmed Halawa
Journal:  World J Transplant       Date:  2017-04-24

5.  A 3-month, Multicenter, Randomized, Open-label Study to Evaluate the Impact on Wound Healing of the Early (vs Delayed) Introduction of Everolimus in De Novo Kidney Transplant Recipients, With a Follow-up Evaluation at 12 Months After Transplant (NEVERWOUND Study).

Authors:  Tommaso Maria Manzia; Mario Carmellini; Paola Todeschini; Antonio Secchi; Silvio Sandrini; Enrico Minetti; Lucrezia Furian; Gionata Spagnoletti; Francesco Pisani; Gian Benedetto Piredda; Gianni Cappelli; GIuseppe Tisone
Journal:  Transplantation       Date:  2020-02       Impact factor: 5.385

6.  Design and rationale of the ATHENA study--A 12-month, multicentre, prospective study evaluating the outcomes of a de novo everolimus-based regimen in combination with reduced cyclosporine or tacrolimus versus a standard regimen in kidney transplant patients: study protocol for a randomised controlled trial.

Authors:  Claudia Sommerer; Barbara Suwelack; Duska Dragun; Peter Schenker; Ingeborg A Hauser; Björn Nashan; Friedrich Thaiss
Journal:  Trials       Date:  2016-02-17       Impact factor: 2.279

  6 in total

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