Safety of sofosbuvir-based regimens after ...
Document type :
Article dans une revue scientifique
DOI :
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Title :
Safety of sofosbuvir-based regimens after liver transplantation: longitudinal assessment of renal function in the prospective ANRS CO23 CUPILT study.
Author(s) :
Anty, Rodolphe [Auteur]
Favre, G [Auteur]
Coilly, Audrey [Auteur]
Rossignol, Emilie [Auteur]
Houssel-Debry, Pauline [Auteur]
Duvoux, Christophe [Auteur]
De Ledinghen, Victor [Auteur]
Di Martino, Vincent [Auteur]
Leroy, Vincent [Auteur]
Radenne, Sylvie [Auteur]
Kamar, Nassim [Auteur]
Canva, Valerie [Auteur]
D'alteroche, Louis [Auteur]
Durand, Francois [Auteur]
Dumortier, Jerome [Auteur]
Lebray, Pascal [Auteur]
Besch, Camille [Auteur]
Tran, Albert [Auteur]
Canivet C, M [Auteur]
Botta-Fridlund, Danielle [Auteur]
Montialoux, Helene [Auteur]
Moreno, Christophe [Auteur]
Conti, Filomena [Auteur]
Silvain, Christine [Auteur]
Perre, Philippe [Auteur]
Habersetzer, Francois [Auteur]
Abergel, Armand [Auteur]
Debette-Gratien, Maryline [Auteur]
Dharancy, Sebastien [Auteur]
Lille Inflammation Research International Center - U 995 [LIRIC]
Esnault V L, M [Auteur]
Fougerou-Leurent, Claire [Auteur]
Cagnot, Carole [Auteur]
Diallo, Alpha [Auteur]
Veislinger, A [Auteur]
Danjou, H [Auteur]
Samuel, Didier [Auteur]
Pageaux, Georges-Philippe [Auteur]
Duclos-Vallee, Jean-Charles [Auteur]
Favre, G [Auteur]
Coilly, Audrey [Auteur]
Rossignol, Emilie [Auteur]
Houssel-Debry, Pauline [Auteur]
Duvoux, Christophe [Auteur]
De Ledinghen, Victor [Auteur]
Di Martino, Vincent [Auteur]
Leroy, Vincent [Auteur]
Radenne, Sylvie [Auteur]
Kamar, Nassim [Auteur]
Canva, Valerie [Auteur]
D'alteroche, Louis [Auteur]
Durand, Francois [Auteur]
Dumortier, Jerome [Auteur]
Lebray, Pascal [Auteur]
Besch, Camille [Auteur]
Tran, Albert [Auteur]
Canivet C, M [Auteur]
Botta-Fridlund, Danielle [Auteur]
Montialoux, Helene [Auteur]
Moreno, Christophe [Auteur]
Conti, Filomena [Auteur]
Silvain, Christine [Auteur]
Perre, Philippe [Auteur]
Habersetzer, Francois [Auteur]
Abergel, Armand [Auteur]
Debette-Gratien, Maryline [Auteur]
Dharancy, Sebastien [Auteur]

Lille Inflammation Research International Center - U 995 [LIRIC]
Esnault V L, M [Auteur]
Fougerou-Leurent, Claire [Auteur]
Cagnot, Carole [Auteur]
Diallo, Alpha [Auteur]
Veislinger, A [Auteur]
Danjou, H [Auteur]
Samuel, Didier [Auteur]
Pageaux, Georges-Philippe [Auteur]
Duclos-Vallee, Jean-Charles [Auteur]
Journal title :
Alimentary Pharmacology and Therapeutics
Abbreviated title :
Aliment. Pharmacol. Ther.
Volume number :
47
Pages :
1682-1689
Publication date :
2018-06
ISSN :
1365-2036
HAL domain(s) :
Sciences du Vivant [q-bio]
English abstract : [en]
BACKGROUND: In liver transplant recipients with hepatitis C virus recurrence, there is concern about renal safety of sofosbuvir-based regimens. Changes in serum creatinine or in the estimated glomerular filtration rate ...
Show more >BACKGROUND: In liver transplant recipients with hepatitis C virus recurrence, there is concern about renal safety of sofosbuvir-based regimens. Changes in serum creatinine or in the estimated glomerular filtration rate (eGFR) under treatment are used to look for possible renal toxicity. However, serum creatinine and eGFR are highly variable. AIM: To analyse renal function trajectory with numerous assays of serum creatinine over a long period of time. METHODS: In a multicentre cohort of 139 patients, the eGFR was obtained from serum creatinine using the Chronic Kidney Disease-Epidemiology Collaboration (CKD-EPI) equation. Slopes of eGFR were defined as a change in eGFR during a period divided by time. Pre-treatment, on-treatment and post-treatment periods were 9 months, 3-9 months and 4.5 months. Interactions between eGFR slopes and the pre-treatment eGFR, use of ribavirin or mycophenolate mofetil, and stage of fibrosis were addressed. On-treatment eGFR slopes were separated in tertiles. Pre- and post-treatment eGFR slopes were compared globally and according to tertiles. RESULTS: The post-treatment eGFR slope was significantly better than pre-treatment eGFR slope (+0.18 (IQR -0.76 to +1.32) vs -0.11 (IQR -1.01 to +0.73) mL/min/1.73 m(2) /month, P = 0.03) independently of the pre-treatment eGFR (P = 0.99), ribavirin administration (P = 0.26), mycophenolate mofetil administration (P = 0.51) and stage of fibrosis (F3 and F4 vs lower stages, P = 0.18; F4 vs lower stages, P = 0.08; F4 Child-Pugh B and C vs lower stages, P = 0.38). Tertiles of on-treatment eGFR slopes were -1.71 (IQR -2.54 to -1.48), -0.78 (IQR -1.03 to -0.36) and +0.75 (IQR +0.28 to +1.47) mL/min/1.73 m(2) /month. Pre- and post-treatment eGFR slopes were not significantly different according to tertiles (respectively, P = 0.34, 0.08, 0.73). CONCLUSION: The eGFR varies during treatment and gives a confusing picture of the renal safety of sofosbuvir-based regimens. In contrast, longitudinal assessment of the eGFR shows a rising trajectory over longer time, meaning that these therapies are safe for the kidneys in our cohort of liver transplant recipients.Show less >
Show more >BACKGROUND: In liver transplant recipients with hepatitis C virus recurrence, there is concern about renal safety of sofosbuvir-based regimens. Changes in serum creatinine or in the estimated glomerular filtration rate (eGFR) under treatment are used to look for possible renal toxicity. However, serum creatinine and eGFR are highly variable. AIM: To analyse renal function trajectory with numerous assays of serum creatinine over a long period of time. METHODS: In a multicentre cohort of 139 patients, the eGFR was obtained from serum creatinine using the Chronic Kidney Disease-Epidemiology Collaboration (CKD-EPI) equation. Slopes of eGFR were defined as a change in eGFR during a period divided by time. Pre-treatment, on-treatment and post-treatment periods were 9 months, 3-9 months and 4.5 months. Interactions between eGFR slopes and the pre-treatment eGFR, use of ribavirin or mycophenolate mofetil, and stage of fibrosis were addressed. On-treatment eGFR slopes were separated in tertiles. Pre- and post-treatment eGFR slopes were compared globally and according to tertiles. RESULTS: The post-treatment eGFR slope was significantly better than pre-treatment eGFR slope (+0.18 (IQR -0.76 to +1.32) vs -0.11 (IQR -1.01 to +0.73) mL/min/1.73 m(2) /month, P = 0.03) independently of the pre-treatment eGFR (P = 0.99), ribavirin administration (P = 0.26), mycophenolate mofetil administration (P = 0.51) and stage of fibrosis (F3 and F4 vs lower stages, P = 0.18; F4 vs lower stages, P = 0.08; F4 Child-Pugh B and C vs lower stages, P = 0.38). Tertiles of on-treatment eGFR slopes were -1.71 (IQR -2.54 to -1.48), -0.78 (IQR -1.03 to -0.36) and +0.75 (IQR +0.28 to +1.47) mL/min/1.73 m(2) /month. Pre- and post-treatment eGFR slopes were not significantly different according to tertiles (respectively, P = 0.34, 0.08, 0.73). CONCLUSION: The eGFR varies during treatment and gives a confusing picture of the renal safety of sofosbuvir-based regimens. In contrast, longitudinal assessment of the eGFR shows a rising trajectory over longer time, meaning that these therapies are safe for the kidneys in our cohort of liver transplant recipients.Show less >
Language :
Anglais
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
Inserm
Université de Lille
CHU Lille
Université de Lille
CHU Lille
Research team(s) :
Inflammatory digestive disease : pathophysiology and therapeutic targets developement
Submission date :
2019-03-01T14:17:51Z
2024-01-30T10:23:43Z
2024-01-30T10:23:43Z