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Slow achievement of HCV-RNA undetectability in cirrhotic patients treated with sofosbuvir+ribavirin: possible clinical implications in the liver transplant list management

Authors :
V.C. Di Maio
Francesca Ceccherini-Silberstein
Ilaria Lenci
Luciano Milanesi
Maria Chiara Colombo
M. Manuelli
Maria Francesca Donato
A. Castellaneta
Roberta Alfieri
M. Rendina
Martina Milana
Maria Laura Ponti
R. Canu
A. Di Leo
C.F. Perno
R. Ganga
Federica Malinverno
S. Monico
Mario Angelico
Valeria Cento
Daniele Sforza
Marianna Aragri
A. Abedrabbo
Giuseppe Tisone
Source :
48th A.I.S.F.-Italian Association for the Study of the Liver, pp. 29–30, Roma, 2015, info:cnr-pdr/source/autori:I. Lenci, V. Cento, M. Rendina, M.F. Donato, M. Milana, D. Sforza, M. Manuelli, M. Aragri, V.C. Di Maio, A. Abedrabbo, A. Castellaneta, F. Malinverno, S. Monico, M.L. Ponti, R. Canu, R. Ganga, R. Alfieri, L. Milanesi, A. Di Leo, G. Tisone, C.F. Perno, F. Ceccherini-Silberstein, M. Colombo, M. Angelico/congresso_nome:48th A.I.S.F.-Italian Association for the Study of the Liver/congresso_luogo:Roma/congresso_data:2015/anno:2015/pagina_da:29/pagina_a:30/intervallo_pagine:29–30
Publication Year :
2015
Publisher :
Editrice Gastroenterologica Italiana., Ospedaletto, Pisa , Italia, 2015.

Abstract

Sofosbuvir (SOF) treatment ± ribavirin (RBV) prior to LT has the potential to change the HCV recurrence after Liver Transplantation (LT). This approach has been reported to avoid graft reinfection in compensated patients with hepatocellular carcinoma (HCC), but only among those who reached and maintained undetectable HCV-RNA (TND) before LT. Since the time to obtain this result in decompensated cirrhotics is unknown, we sought to investigate the early HCV-RNA decay in this setting. Sixteen decompensated patients (M/F 12/4, median age 55.3, CPT score>=B7), infected by HCV genotype 1a, 1b, 3 and 4 (2-8- 4-2), 4 of whom with HCC, were treated with SOF 400mg/day and RBV (200-1000 mg/day), except 2 who received SOF alone, for a median(IQR) of 12(11-16) weeks awaiting LT. HCV-RNA levels were measured weekly and safety and clinical parameters were analyzed. No serious adverse events were reported. The median(IQR) RBV dose was 600(400-800). Despite 11/16 patients had low baseline viremia (

Details

Language :
English
Database :
OpenAIRE
Journal :
48th A.I.S.F.-Italian Association for the Study of the Liver, pp. 29–30, Roma, 2015, info:cnr-pdr/source/autori:I. Lenci, V. Cento, M. Rendina, M.F. Donato, M. Milana, D. Sforza, M. Manuelli, M. Aragri, V.C. Di Maio, A. Abedrabbo, A. Castellaneta, F. Malinverno, S. Monico, M.L. Ponti, R. Canu, R. Ganga, R. Alfieri, L. Milanesi, A. Di Leo, G. Tisone, C.F. Perno, F. Ceccherini-Silberstein, M. Colombo, M. Angelico/congresso_nome:48th A.I.S.F.-Italian Association for the Study of the Liver/congresso_luogo:Roma/congresso_data:2015/anno:2015/pagina_da:29/pagina_a:30/intervallo_pagine:29–30
Accession number :
edsair.doi.dedup.....6dfe0677d475a76020acd9244bd54c83
Full Text :
https://doi.org/10.1016/j.dld.2015.01.066