A randomized trial of everolimus-based quadruple therapy vs standard triple therapy early after lung transplantation.
Calcineurin Inhibitors
/ administration & dosage
Drug Administration Schedule
Everolimus
/ administration & dosage
Female
Germany
Glomerular Filtration Rate
Graft Rejection
/ prevention & control
Graft Survival
Humans
Immunosuppressive Agents
/ administration & dosage
Kidney
/ drug effects
Lung Transplantation
Male
Middle Aged
Prospective Studies
Treatment Outcome
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
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
1759-1769Subventions
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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