TY - JOUR
T1 - Role of Etiology in Hepatocellular Carcinoma Patients Treated with Lenvatinib
T2 - A Counterfactual Event-Based Mediation Analysis
AU - on behalf of A.I.G.O. (Italian Association of Hospital Gastroenterologists)
AU - Sacco, Rodolfo
AU - Ramai, Daryl
AU - Tortora, Raffaella
AU - di Costanzo, Giovan Giuseppe
AU - Burlone, Michela Emma
AU - Pirisi, Mario
AU - Federico, Piera
AU - Daniele, Bruno
AU - Silletta, Marianna
AU - Gallo, Paolo
AU - Cocuzza, Caterina
AU - Russello, Maurizio
AU - Cabibbo, Giuseppe
AU - Rancatore, Gabriele
AU - Cesario, Silvia
AU - Masi, Gianluca
AU - Marzi, Luca
AU - Mega, Andrea
AU - Granito, Alessandro
AU - Pieri, Giulia
AU - Giannini, Edoardo G.
AU - Paolillo, Rosa
AU - Gadaleta-Caldarola, Gennaro
AU - Dadduzio, Vincenzo
AU - Giordano, Guido
AU - Giacomelli, Luca
AU - Papa, Simonetta
AU - Renzulli, Matteo
AU - Maida, Marcello
AU - Ghidini, Michele
AU - Borzio, Mauro
AU - Facciorusso, Antonio
N1 - Publisher Copyright:
© 2023 by the authors.
PY - 2023/1
Y1 - 2023/1
N2 - Background: Whether the etiology of underlying liver disease represents a prognostic factor in patients with hepatocellular carcinoma (HCC) treated with lenvatinib is still a matter of debate. This study investigates whether the viral etiology of HCC plays a prognostic role in overall survival (OS). Methods: Data derived from a multicenter series of 313 HCC patients treated with lenvatinib between 2019 and 2022 were analyzed. Actuarial survival estimates were computed using the Kaplan–Meier method and compared with the log-rank test. We performed an event-based counterfactual mediation analysis to estimate direct (chronic inflammation and immunosuppression), indirect (tobacco smoking, alcohol use, illicit drug abuse with injections), and the total effect of viral etiology on OS. Results were expressed as hazard ratio (HR) and 95% CI. Results: Median OS was 21 months (95% CI: 20–23) in the group with other etiologies and 15 months (14–16) in the group with viral etiology (p < 0.0001). The total effect of viral etiology was associated with OS (HR 2.76, 1.32–5.21), and it was mainly explained by the pure direct effect of viral etiology (HR 2.74, 1.15–4.45). By contrast, its total indirect effect was not associated with poorer survival (HR 1.05, 0.82–2.13). These results were confirmed when considering tobacco, alcohol consumption, or injection drug abuse as potential mediators. Median progression-free survival was 9 months (8–10) in patients with other etiologies and 6 months (5–7) in patients with viral etiology (p < 0.0001). No difference in terms of adverse event rate was observed between the two groups. Conclusions: Patients affected by HCC with nonviral etiology treated with lenvatinib exhibit longer survival than those with viral etiology. This finding may have relevance in the treatment decision-making process.
AB - Background: Whether the etiology of underlying liver disease represents a prognostic factor in patients with hepatocellular carcinoma (HCC) treated with lenvatinib is still a matter of debate. This study investigates whether the viral etiology of HCC plays a prognostic role in overall survival (OS). Methods: Data derived from a multicenter series of 313 HCC patients treated with lenvatinib between 2019 and 2022 were analyzed. Actuarial survival estimates were computed using the Kaplan–Meier method and compared with the log-rank test. We performed an event-based counterfactual mediation analysis to estimate direct (chronic inflammation and immunosuppression), indirect (tobacco smoking, alcohol use, illicit drug abuse with injections), and the total effect of viral etiology on OS. Results were expressed as hazard ratio (HR) and 95% CI. Results: Median OS was 21 months (95% CI: 20–23) in the group with other etiologies and 15 months (14–16) in the group with viral etiology (p < 0.0001). The total effect of viral etiology was associated with OS (HR 2.76, 1.32–5.21), and it was mainly explained by the pure direct effect of viral etiology (HR 2.74, 1.15–4.45). By contrast, its total indirect effect was not associated with poorer survival (HR 1.05, 0.82–2.13). These results were confirmed when considering tobacco, alcohol consumption, or injection drug abuse as potential mediators. Median progression-free survival was 9 months (8–10) in patients with other etiologies and 6 months (5–7) in patients with viral etiology (p < 0.0001). No difference in terms of adverse event rate was observed between the two groups. Conclusions: Patients affected by HCC with nonviral etiology treated with lenvatinib exhibit longer survival than those with viral etiology. This finding may have relevance in the treatment decision-making process.
KW - HBV
KW - HCC
KW - HCV
KW - liver cancer
KW - mediation analysis
KW - nonviral liver disease
KW - progression
KW - survival
KW - viral etiology
UR - https://www.scopus.com/pages/publications/85146797581
U2 - 10.3390/cancers15020381
DO - 10.3390/cancers15020381
M3 - Article
SN - 2072-6694
VL - 15
JO - Cancers
JF - Cancers
IS - 2
M1 - 381
ER -