Lenvatinib versus sorafenib in first-line treatment of patients with unresectable hepatocellular carcinoma: a randomised phase 3 non-inferiority trial

In a phase 2 trial, lenvatinib, an inhibitor of VEGF receptors 1–3, FGF receptors 1–4, PDGF receptor α, RET, and KIT, showed activity in hepatocellular carcinoma. We aimed to compare overall survival in patients treated with lenvatinib versus sorafenib as a first-line treatment for unresectable hepa...

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Veröffentlicht in:The Lancet (British edition) 2018-03, Vol.391 (10126), p.1163-1173
Hauptverfasser: Kudo, Masatoshi, Finn, Richard S, Qin, Shukui, Han, Kwang-Hyub, Ikeda, Kenji, Piscaglia, Fabio, Baron, Ari, Park, Joong-Won, Han, Guohong, Jassem, Jacek, Blanc, Jean Frederic, Vogel, Arndt, Komov, Dmitry, Evans, T R Jeffry, Lopez, Carlos, Dutcus, Corina, Guo, Matthew, Saito, Kenichi, Kraljevic, Silvija, Tamai, Toshiyuki, Ren, Min, Cheng, Ann-Lii
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Sprache:eng
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Zusammenfassung:In a phase 2 trial, lenvatinib, an inhibitor of VEGF receptors 1–3, FGF receptors 1–4, PDGF receptor α, RET, and KIT, showed activity in hepatocellular carcinoma. We aimed to compare overall survival in patients treated with lenvatinib versus sorafenib as a first-line treatment for unresectable hepatocellular carcinoma. This was an open-label, phase 3, multicentre, non-inferiority trial that recruited patients with unresectable hepatocellular carcinoma, who had not received treatment for advanced disease, at 154 sites in 20 countries throughout the Asia-Pacific, European, and North American regions. Patients were randomly assigned (1:1) via an interactive voice–web response system—with region; macroscopic portal vein invasion, extrahepatic spread, or both; Eastern Cooperative Oncology Group performance status; and bodyweight as stratification factors—to receive oral lenvatinib (12 mg/day for bodyweight ≥60 kg or 8 mg/day for bodyweight
ISSN:0140-6736
1474-547X
DOI:10.1016/S0140-6736(18)30207-1