Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster Display & Cocktail

56P - Comparative analysis of HAIC combined with targeted therapy versus immunotherapy combination in advanced HCC patients with lenvatinib failure

Date

03 Mar 2025

Session

Poster Display & Cocktail

Presenters

Jinpeng Li

Citation

Annals of Oncology (2025) 10 (suppl_2): 1-8. 10.1016/esmoop/esmoop104198

Authors

J. Li1, J. song2

Author affiliations

  • 1 Surgical Oncology Department, Shandong Cancer Hospital and Institute, 250117 - Jinan/CN
  • 2 Oncology Department, Shandong Cancer Hospital and Institute, 250117 - Jinan/CN

Resources

This content is available to ESMO members and event participants.

Abstract 56P

Background

The optimal treatment strategy for advanced hepatocellular carcinoma (HCC) after lenvatinib failure remains unclear. This study aimed to compare the efficacy and safety of hepatic arterial infusion chemotherapy (HAIC) combined with either targeted therapy or immunotherapy combination in these patients.

Methods

We conducted a retrospective study of 49 patients with advanced HCC who experienced disease progression after lenvatinib treatment between February 2023 and February 2024. Patients were divided into two groups: HAIC plus lenvatinib (H+T group, n=18) and HAIC plus sintilimab and bevacizumab (H+I group, n=31). The primary endpoints were objective response rate (ORR) and progression-free survival (PFS). Secondary endpoints included disease control rate (DCR), overall survival (OS), and safety.

Results

The ORR was 22.2% in the H+T group versus 35.5% in the H+I group (p=0.534). The DCR was 88.9% versus 83.8% respectively (p=0.889). Median PFS was 10.1 months (95% CI: 8.3-11.9) in the H+T group versus 12.0 months (95% CI: 9.4-14.6) in the H+I group. Median OS was 15.9 months (95% CI: 11.5-20.3) versus 18.1 months (95% CI: 13.3-22.9) respectively. Both groups showed significant decreases in CEA, VEGF, and CA125 levels after treatment (p<0.05), with the H+I group showing more pronounced reductions. The incidence of adverse events was comparable between groups, with no significant differences in the safety profile.

Conclusions

HAIC combined with sintilimab and bevacizumab showed a trend toward improved ORR and survival outcomes compared to HAIC plus lenvatinib in advanced HCC patients after lenvatinib failure, with manageable safety profiles in both groups. These findings warrant further investigation in larger prospective studies.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.