A randomized trial of everolimus-based quadruple therapy vs standard triple therapy early after lung transplantation.

clinical research/practice cyclosporine A (CsA) everolimus immunosuppressant - calcineurin inhibitor immunosuppressant - mechanistic target of rapamycin immunosuppressant - mechanistic target of rapamycin (mTOR) immunosuppression/immune modulation lung transplantation/pulmonology rejection tacrolimus

Journal

American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
ISSN: 1600-6143
Titre abrégé: Am J Transplant
Pays: United States
ID NLM: 100968638

Informations de publication

Date de publication:
06 2019
Historique:
received: 25 10 2018
revised: 04 12 2018
accepted: 27 12 2018
pubmed: 8 1 2019
medline: 13 8 2020
entrez: 8 1 2019
Statut: ppublish

Résumé

Calcineurin inhibitor (CNI) therapy after lung transplantation increases risk of kidney failure. Early everolimus-based quadruple low CNI immunosuppression may improve renal function without compromising efficacy or safety. A prospective, randomized, open-label, 12-month multicenter trial was conducted at 8 German sites. Patients 3-18 months after lung transplantation were randomized (1:1), stratified by baseline estimated glomerular filtration rate (eGFR). In the quadruple low CNI regimen, patients received everolimus (target trough level 3-5 ng/mL) with reduced CNI (tacrolimus 3-5 ng/mL or cyclosporine 25-75 ng/mL) and a cell cycle inhibitor plus prednisone. In the standard triple CNI regimen, patients received tacrolimus (target trough level >5 ng/mL) or cyclosporine (>100 ng/mL) and a cell cycle inhibitor plus prednisone. Of the 180 patients screened, 130 were randomized: 67 in the quadruple low CNI group and 63 in the standard triple CNI group. The primary endpoint (eGFR after 12 months) demonstrated superiority of the quadruple low CNI regimen: 64.5 mL/min vs 54.6 mL/min for the standard triple group (least squares mean, analysis of covariance; P < .001). Key efficacy parameters (biopsy-proven acute rejection, chronic lung allograft dysfunction, and death) and safety endpoints were similar between both groups. Quadruple low CNI immunosuppression early after lung transplantation was demonstrated to be efficacious and safe. Clinical trials registry: ClinicalTrials.gov NCT01404325.

Identifiants

pubmed: 30615259
doi: 10.1111/ajt.15251
pmc: PMC6590654
pii: S1600-6135(22)09119-5
doi:

Substances chimiques

Calcineurin Inhibitors 0
Immunosuppressive Agents 0
Everolimus 9HW64Q8G6G

Banques de données

ClinicalTrials.gov
['NCT01404325']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1759-1769

Subventions

Organisme : Novartis Pharma GmbH, Nuremberg, Germany
Pays : International

Informations de copyright

© 2019 The Authors. American Journal of Transplantation published by Wiley Periodicals, Inc. on behalf of The American Society of Transplantation and the American Society of Transplant Surgeons.

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Auteurs

Jens Gottlieb (J)

Department of Respiratory Medicine, Hannover Medical School, Hannover, Germany.
Biomedical Research in Endstage and Obstructive Lung Disease Hannover (BREATH), Member of the German Center for Lung Research (DZL), Hannover, Germany.

Claus Neurohr (C)

Grosshadern Medical Clinic and Policlinic V, LMU Munich University Hospital, Munich, Germany.

Joachim Müller-Quernheim (J)

Pulmonology Medical Clinic, Freiburg University Hospital, Freiburg, Germany.

Hubert Wirtz (H)

Internal Medicine/Department of Pneumology, Leipzig University Hospital, Leipzig, Germany.

Bjoern Sill (B)

Department of Cardiovascular Surgery, Hamburg-Eppendorf University Hospital, Hamburg, Germany.

Heinrike Wilkens (H)

Internal Medicine V, University Hospital of Saarland, Homburg Saar, Germany.

Vasiliki Bessa (V)

Department of Pneumology, Ruhrlandklinik, West German Center for Lung Transplantation, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Christoph Knosalla (C)

Department of Cardiothoracic and Vascular Surgery, German Heart Institute Berlin, DZHK (German Center for Cardiovascular Research), Berlin, Germany.

Martina Porstner (M)

Novartis Pharma GmbH, Nuremberg, Germany.

Carmen Capusan (C)

Novartis Pharma GmbH, Nuremberg, Germany.

Martin Strüber (M)

Department of Cardiothoracic Surgery, Newark Beth Israel Medical Center, Children's Hospital of New Jersey, Newark, New Jersey.

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Classifications MeSH