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.

Real-Life Clinical Data of Lenvatinib versus Sorafenib for Unresectable Hepatocellular Carcinoma in Italy / Burgio V.; Iavarone M.; Di Costanzo G.G.; Marra F.; Lonardi S.; Tamburini E.; Piscaglia F.; Masi G.; Celsa C.; Foschi F.G.; Silletta M.; Amoruso D.C.; Rimini M.; Bruccoleri M.; Tortora R.; Campani C.; Solda C.; Viola M.G.; Forgione A.; Conti F.; Salani F.; Catanese S.; Giacchetto C.M.; Fulgenzi C.; Coppola C.; Lampertico P.; Pellino A.; Rancatore G.; Cabibbo G.; Ratti F.; Pedica F.; Della Corte A.; Colombo M.; De Cobelli F.; Aldrighetti L.; Cascinu S.; Casadei-Gardini A.. - In: CANCER MANAGEMENT AND RESEARCH. - ISSN 1179-1322. - STAMPA. - 13:(2021), pp. 9379-9389. [10.2147/CMAR.S330195]

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

Marra F.;Campani C.;
2021

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.
2021
13
9379
9389
Burgio V.; Iavarone M.; Di Costanzo G.G.; Marra F.; Lonardi S.; Tamburini E.; Piscaglia F.; Masi G.; Celsa C.; Foschi F.G.; Silletta M.; Amoruso D.C.; Rimini M.; Bruccoleri M.; Tortora R.; Campani C.; Solda C.; Viola M.G.; Forgione A.; Conti F.; Salani F.; Catanese S.; Giacchetto C.M.; Fulgenzi C.; Coppola C.; Lampertico P.; Pellino A.; Rancatore G.; Cabibbo G.; Ratti F.; Pedica F.; Della Corte A.; Colombo M.; De Cobelli F.; Aldrighetti L.; Cascinu S.; Casadei-Gardini A.
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1261551
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