Home > Oncology > ASCO GI 2023 > Hepatobiliary Cancer > Improved survival following postoperative sorafenib plus TACE in HCC

Improved survival following postoperative sorafenib plus TACE in HCC

Presented by
Prof. Ming Kuang, The First Affiliated Hospital, China
Conference
ASCO GI 2023
Doi
https://doi.org/10.55788/30fb3fda

The postoperative adjuvant combination therapy of sorafenib plus transarterial chemoembolisation (TACE) proved to be superior to sorafenib alone in patients with hepatocellular carcinoma (HCC) and portal vein tumour thrombus (PVTT) after surgery in a phase 3 study.

Prof. Ming Kuang (The First Affiliated Hospital, China) and colleagues designed a phase 3 trial to assess the efficacy and safety of sorafenib plus TACE as a post-operative adjuvant treatment in patients with HCC and PVTT after surgery (n=158) [1]. The included patients were randomised 1:1 to sorafenib only or to sorafenib plus TACE. Recurrence-free survival (RFS) was the primary endpoint of the trial.

The RFS was significantly improved in patients receiving the combination therapy compared with those receiving sorafenib only (median RFS 16.8 months vs 12.6 months; HR 0.57; 95% CI 0.39–0.83; Log-rank P=0.0024). The median overall survival (OS) was longer in patients in the sorafenib plus TACE arm than in patients in the sorafenib-only arm (30.4 months vs 22.5 months; HR 0.57; 95% CI 0.36–0.91; Log-rank P=0.0174). Prof. Kuang added that sorafenib plus TACE was well tolerated and that the safety profiles of the 2 treatment regimens were similar.

The improved RFS and OS in patients receiving sorafenib and TACE indicate that this combination therapy may provide an effective strategy to control advanced HCC after surgery. Of note, this data concerns a niche of patients with PVTT and currently adjuvant treatment even with sorafenib is not recommended by NCCN guidelines (NCCN version 5.2002).

  1. Peng Z, et al. Adjuvant Transarterial Chemoembolization with Sorafenib for Hepatocellular Carcinoma Patients with Portal Vein Tumor Thrombus after Surgery: A Phase III, Multicenter, Randomized, Controlled Trial. Abstract 493, ASCO GI 2023, 19–21 January, San Francisco, CA, USA.

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