%0 Journal Article %A Sapena, Victor %A Enea, Marco %A Torres, Ferran %A Celsa, Ciro %A Rios, Jose %A Rizzo, Giacomo Emanuele Maria %A Nahon, Pierre %A Mariño, Zoe %A Tateishi, Ryosuke %A Minami, Tatsuya %A Sangiovanni, Angelo %A Forns, Xavier %A Toyoda, Hidenori %A Brillanti, Stefano %A Conti, Fabio %A Degasperi, Elisabetta %A Yu, Ming-Lung %A Tsai, Pei-Chien %A Jean, Kevin %A El Kassas, Mohamed %A Shousha, Hend Ibrahim %A Omar, Ashraf %A Zavaglia, Claudio %A Nagata, Hiroko %A Nakagawa, Mina %A Asahina, Yasuhiro %A Singal, Amit G %A Murphy, Caitlin %A Kohla, Mohamed %A Masetti, Chiara %A Dufour, Jean-François %A Merchante, Nicolas %A Cavalletto, Luisa %A Chemello, Liliana Lc %A Pol, Stanislas %A Crespo, Javier %A Calleja, Jose Luis %A Villani, Rosanna %A Serviddio, Gaetano %A Zanetto, Alberto %A Shalaby, Sarah %A Russo, Francesco Paolo %A Bielen, Rob %A Trevisani, Franco %A Cammà, Calogero %A Bruix, Jordi %A Cabibbo, Giuseppe %A Reig, Maria %T Hepatocellular carcinoma recurrence after direct-acting antiviral therapy: an individual patient data meta-analysis. %D 2021 %U http://hdl.handle.net/10668/20154 %X The benefit of direct-acting antivirals (DAAs) against HCV following successful treatment of hepatocellular carcinoma (HCC) remains controversial. This meta-analysis of individual patient data assessed HCC recurrence risk following DAA administration. We pooled the data of 977 consecutive patients from 21 studies of HCV-related cirrhosis and HCC, who achieved complete radiological response after surgical/locoregional treatments and received DAAs (DAA group). Recurrence or death risk was expressed as HCC recurrence or death per 100 person-years (100PY). Propensity score-matched patients from the ITA.LI.CA. cohort (n=328) served as DAA-unexposed controls (no-DAA group). Risk factors for HCC recurrence were identified using random-effects Poisson. Recurrence rate and death risk per 100PY in DAA-treated patients were 20 (95% CI 13.9 to 29.8, I2=74.6%) and 5.7 (2.5 to 15.3, I2=54.3), respectively. Predictive factors for recurrence were alpha-fetoprotein logarithm (relative risk (RR)=1.11, 95% CI 1.03 to 1.19; p=0.01, per 1 log of ng/mL), HCC recurrence history pre-DAA initiation (RR=1.11, 95% CI 1.07 to 1.16; p Effects of DAA exposure on HCC recurrence risk remain inconclusive. Active clinical and radiological follow-up of patients with HCC after HCV eradication with DAA is justified. %K antiviral therapy %K hepatocellular carcinoma %K meta-analysis %~