Redefining Therapeutic Drug Monitoring of Tacrolimus in Patients Undergoing Liver Transplantation: A Target Trough Concentration of 4-7 ng/mL During the First Month After Liver Transplantation is Safe and Improves Graft and Renal Function.


Journal

Therapeutic drug monitoring
ISSN: 1536-3694
Titre abrégé: Ther Drug Monit
Pays: United States
ID NLM: 7909660

Informations de publication

Date de publication:
10 2020
Historique:
entrez: 17 9 2020
pubmed: 18 9 2020
medline: 19 8 2021
Statut: ppublish

Résumé

Currently, the recommended tacrolimus (TAC) trough level (Cmin) after liver transplantation (LT) is 6-10 ng/mL (when associated in triple immunosuppressive therapy). However, few studies have achieved the lower limit of this range, especially below 7 ng/mL. This study evaluated the efficacy of a target TAC Cmin of 4-7 ng/mL after LT. Of 1677 LTs performed between 2002 and 2017, 904 LT cases were analyzed. The cases were categorized into the following 3 groups and compared: low- (n = 247, 27.3%), intermediate- (n = 344, 37.9%), and high-exposure groups (n = 313, 34.5%) with TAC Cmin of 4-7 ng/mL, 7-10 ng/mL, and >10 ng/mL, respectively. In addition, propensity score matching was performed to reduce heterogeneity and population bias. At months 1 and 3, when compared with the 2 other groups, the low-exposure group had similar grafts (P = 0.75) and patient (P = 0.77) survival, but lower alanine aminotransferase (P < 0.001), bilirubin (P < 0.001), international normalized ratio (P = 0.046), and creatinine (P < 0.001) levels. After propensity score matching, the bilirubin (P < 0.001) and creatinine (P = 0.001) levels in the low-exposure group still improved at months 3, but the graft (P = 0.86) and patient (P = 0.99) survival were still similar. A TAC Cmin of 4-7 ng/mL seems safe and capable of improving graft and kidney function. This finding should be confirmed in a prospective randomized trial.

Sections du résumé

BACKGROUND
Currently, the recommended tacrolimus (TAC) trough level (Cmin) after liver transplantation (LT) is 6-10 ng/mL (when associated in triple immunosuppressive therapy). However, few studies have achieved the lower limit of this range, especially below 7 ng/mL. This study evaluated the efficacy of a target TAC Cmin of 4-7 ng/mL after LT.
METHODS
Of 1677 LTs performed between 2002 and 2017, 904 LT cases were analyzed. The cases were categorized into the following 3 groups and compared: low- (n = 247, 27.3%), intermediate- (n = 344, 37.9%), and high-exposure groups (n = 313, 34.5%) with TAC Cmin of 4-7 ng/mL, 7-10 ng/mL, and >10 ng/mL, respectively. In addition, propensity score matching was performed to reduce heterogeneity and population bias.
RESULTS
At months 1 and 3, when compared with the 2 other groups, the low-exposure group had similar grafts (P = 0.75) and patient (P = 0.77) survival, but lower alanine aminotransferase (P < 0.001), bilirubin (P < 0.001), international normalized ratio (P = 0.046), and creatinine (P < 0.001) levels. After propensity score matching, the bilirubin (P < 0.001) and creatinine (P = 0.001) levels in the low-exposure group still improved at months 3, but the graft (P = 0.86) and patient (P = 0.99) survival were still similar.
CONCLUSIONS
A TAC Cmin of 4-7 ng/mL seems safe and capable of improving graft and kidney function. This finding should be confirmed in a prospective randomized trial.

Identifiants

pubmed: 32941395
doi: 10.1097/FTD.0000000000000779
pii: 00007691-202010000-00005
doi:

Substances chimiques

Immunosuppressive Agents 0
Tacrolimus WM0HAQ4WNM

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

671-678

Auteurs

Florian Lemaitre (F)

Université Rennes1, Faculté de Médecine.
INSERM, CIC 1414.
CHU Rennes, Service de Pharmacologie Clinique.

Camille Tron (C)

Université Rennes1, Faculté de Médecine.
INSERM, CIC 1414.
CHU Rennes, Service de Pharmacologie Clinique.

Thomas Renard (T)

CHU Rennes, Service de Chirurgie Hépatobiliaire et Digestive.

Caroline Jézéquel (C)

CHU Rennes, Service des Maladies du Foie.

Pauline Houssel-Debry (P)

CHU Rennes, Service de Chirurgie Hépatobiliaire et Digestive.
CHU Rennes, Service des Maladies du Foie.

Damien Bergeat (D)

Université Rennes1, Faculté de Médecine.
INSERM, CIC 1414.
CHU Rennes, Service de Chirurgie Hépatobiliaire et Digestive.

Cédric Pastoret (C)

CHU Rennes, Service d'Hématologie Cellulaire, Hémostase Bioclinique.

Nicolas Collet (N)

CHU Rennes, Service de Biochimie et Toxicologie.

Antoine Petitcollin (A)

Université Rennes1, Faculté de Médecine.
INSERM, CIC 1414.
CHU Rennes, Service de Pharmacologie Clinique.

Marie-Clémence Verdier (MC)

Université Rennes1, Faculté de Médecine.
INSERM, CIC 1414.
CHU Rennes, Service de Pharmacologie Clinique.

Edouard Bardou-Jacquet (E)

Université Rennes1, Faculté de Médecine.
INSERM, CIC 1414.
CHU Rennes, Service des Maladies du Foie.

Christophe Camus (C)

INSERM, CIC 1414.
CHU Rennes, Service des Maladies Infectieuses et Réanimation Médicale.

Karim Boudjema (K)

Université Rennes1, Faculté de Médecine.
INSERM, CIC 1414.
CHU Rennes, Service de Chirurgie Hépatobiliaire et Digestive.

Eric Bellissant (E)

Université Rennes1, Faculté de Médecine.
INSERM, CIC 1414.
CHU Rennes, Service de Pharmacologie Clinique.

Michel Rayar (M)

Université Rennes1, Faculté de Médecine.
INSERM, CIC 1414.
CHU Rennes, Service de Chirurgie Hépatobiliaire et Digestive.

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