23
Participants
Start Date
June 1, 2018
Primary Completion Date
March 31, 2020
Study Completion Date
March 31, 2020
Lenvatinib
The patients in lenvatinib group received oral lenvatinib (Eisai, Japan) 12 mg/day (for bodyweight (BW) ≥60 kg) or 8 mg/day (for BW \<60 kg) in 28-day cycles until HCC recurrence or serious adverse events (SAEs) or voluntary withdrawal. Dose interruptions followed by reductions for lenvatinib-related toxicities (to 8 mg and 4 mg/day, or 4 mg every other day) were permitted. All 14 patients took lenvatinib for more than 3 cycles.
Xinhua Hospital Affiliated to Shanghai Jiao Tong University Medical School, Shanghai
Jinyang Gu
OTHER