TY - JOUR
T1 - The Role of Salvage Transplantation in Patients Initially Treated With Open Versus Minimally Invasive Liver Surgery
T2 - An Intention-to-Treat Analysis
AU - Levi Sandri, Giovanni B
AU - Lai, Quirino
AU - Ravaioli, Matteo
AU - Di Sandro, Stefano
AU - Balzano, Emanuele
AU - Pagano, Duilio
AU - Magistri, Paolo
AU - Di Benedetto, Fabrizio
AU - Rossi, Massimo
AU - Gruttadauria, Salvatore
AU - De Simone, Paolo
AU - Ettorre, Giuseppe M
AU - De Carlis, Luciano
AU - Cescon, Matteo
AU - Colasanti, Marco
AU - Mennini, Gianluca
AU - Serenari, Matteo
AU - Ferla, Fabio
AU - Tincani, Giovanni
AU - Francesco, Fabrizio Di
AU - Guidetti, Cristiano
N1 - Copyright © 2020 by the American Association for the Study of Liver Diseases.
PY - 2020/7
Y1 - 2020/7
N2 - Despite gaining wide consensus in the management of hepatocellular carcinoma (HCC), minimally invasive liver surgery (MILS) has been poorly investigated for its role in the setting of salvage liver transplantation (SLT). A multicenter retrospective analysis was carried out in 6 Italian centers on 211 patients with HCC who were initially resected with open (n = 167) versus MILS (n = 44) and eventually wait-listed for SLT. The secondary endpoint was identification of risk factors for posttransplant death and tumor recurrence. The enrolled patients included 211 HCC patients resected with open surgery (n = 167) versus MILS (n = 44) and wait-listed for SLT between January 2007 and December 2017. We analyzed the intention-to-treat survival of these patients. MILS was the most important protective factor for the composite risk of delisting, posttransplant patient death, and HCC recurrence (OR, 0.26; 95% confidence interval [CI], 0.11-0.63; P = 0.003). MILS was also the only independent protective factor for the risk of post-SLT patient death (OR, 0.29; 95% CI, 0.09-0.93; P = 0.04). After propensity score matching, MILS was the only independent protective factor against the risk of delisting, posttransplant death, and HCC recurrence (OR, 0.22; 95% CI, 0.07-0.75; P = 0.02). On the basis of the current analysis, MILS seems protective over open surgery for the risk of delisting, posttransplant patient death, and tumor recurrence. Larger prospective studies balancing liver function and tumor stage are strongly favored to better clarify the beneficial effect of MILS for HCC patients eventually referred to SLT.
AB - Despite gaining wide consensus in the management of hepatocellular carcinoma (HCC), minimally invasive liver surgery (MILS) has been poorly investigated for its role in the setting of salvage liver transplantation (SLT). A multicenter retrospective analysis was carried out in 6 Italian centers on 211 patients with HCC who were initially resected with open (n = 167) versus MILS (n = 44) and eventually wait-listed for SLT. The secondary endpoint was identification of risk factors for posttransplant death and tumor recurrence. The enrolled patients included 211 HCC patients resected with open surgery (n = 167) versus MILS (n = 44) and wait-listed for SLT between January 2007 and December 2017. We analyzed the intention-to-treat survival of these patients. MILS was the most important protective factor for the composite risk of delisting, posttransplant patient death, and HCC recurrence (OR, 0.26; 95% confidence interval [CI], 0.11-0.63; P = 0.003). MILS was also the only independent protective factor for the risk of post-SLT patient death (OR, 0.29; 95% CI, 0.09-0.93; P = 0.04). After propensity score matching, MILS was the only independent protective factor against the risk of delisting, posttransplant death, and HCC recurrence (OR, 0.22; 95% CI, 0.07-0.75; P = 0.02). On the basis of the current analysis, MILS seems protective over open surgery for the risk of delisting, posttransplant patient death, and tumor recurrence. Larger prospective studies balancing liver function and tumor stage are strongly favored to better clarify the beneficial effect of MILS for HCC patients eventually referred to SLT.
U2 - 10.1002/lt.25768
DO - 10.1002/lt.25768
M3 - Article
C2 - 32246741
VL - 26
SP - 878
EP - 887
JO - Liver Transplantation
JF - Liver Transplantation
SN - 1527-6465
IS - 7
ER -