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Real-Life Clinical Data of Lenvatinib versus Sorafenib for Unresectable Hepatocellular Carcinoma in Italy

  • Autori: Burgio, Valentina; Iavarone, Massimo; Di Costanzo, Giovanni Giuseppe; Marra, Fabio; Lonardi, Sara; Tamburini, Emiliano; Piscaglia, Fabio; Masi, Gianluca; Celsa, Ciro; Foschi, Francesco Giuseppe; Silletta, Marianna; Amoruso, Daniela Caterina; Rimini, Margherita; Bruccoleri, Mariangela; Tortora, Raffaella; Campani, Claudia; Soldà, Caterina; Viola, Massimo Giuseppe; Forgione, Antonella; Conti, Fabio; Salani, Francesca; Catanese, Silvia; Giacchetto, Carmelo Marco; Fulgenzi, Claudia; Coppola, Carmine; Lampertico, Pietro; Pellino, Antonio; Rancatore, Gabriele; Cabibbo, Giuseppe; Ratti, Francesca; Pedica, Federica; Della Corte, Angelo; Colombo, Massimo; De Cobelli, Francesco; Aldrighetti, Luca; Cascinu, Stefano; Casadei-Gardini, Andrea
  • Anno di pubblicazione: 2021
  • Tipologia: Articolo in rivista
  • OA Link: http://hdl.handle.net/10447/533382

Abstract

Background: Lenvatinib has been approved in Italy since October 2019 as a first-line therapy for advanced hepatocellular carcinoma (HCC) and to date data on effectiveness and safety of lenvatinib are not available in our region. To fill this gap, we performed a multicentric analysis of the real-world treatment outcomes with the propensity score matching in a cohort of Italian patients with unresectable HCC who were treated with either sorafenib or lenvatinib. Aims and Methods: To evaluate the effectiveness of sorafenib and lenvatinib as primary treatment of advanced HCC in clinical practice we performed a multicentric analysis of the treatment outcomes of 288 such patients recruited in 11 centers in Italy. A propensity score was used to mitigate confounding due to referral biases in the assessment of mortality and progression-free survival. Results: Over a follow-up period of 11 months the Cox regression model showed 48% reduction of death risk for patients treated with lenvatinib (95% CI: 0.34-0.81; p = 0.0034), compared with those treated with sorafenib. The median PFS was 9.0 and 4.9 months for lenvatinib and sorafenib arm, respectively. Patients treated with lenvatinib showed a higher percentage of response rate (29.4% vs 2.8%; p < 0.00001) compared with patients treated with sorafenib. Sorafenib was shown to be correlated with more HFSR, diarrhea and fatigue, while lenvatinib with more hypertension and fatigue. Conclusion: Our study highlighted for the first time the efficacy and safety of lenvatinib in an Italian cohort of patients.