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Poster Display session

213P - Duration of adjuvant immune checkpoint inhibitors in hepatocellular carcinoma with high-risk recurrence factors: A prospective, multicentric cohort study

Date

07 Dec 2024

Session

Poster Display session

Presenters

Jia-Yong Su

Citation

Annals of Oncology (2024) 35 (suppl_4): S1450-S1504. 10.1016/annonc/annonc1688

Authors

J. Su1, S. Liu2, X. Xu3, J. Ou4, L. Li5, Y. Ma6, L. Ma1, J. Zhong1

Author affiliations

  • 1 Hepatobiliary Surgery, Guangxi Medical University Cancer Hospital, 530021 - Nanning/CN
  • 2 Hepatobiliary Surgery, The Eighth Affiliated Hospital of Guangxi Medical University, 537100 - Guigang/CN
  • 3 Medical Records And Statistics Room, The People's Hospital of Wuzhou, 543100 - Wuzhou/CN
  • 4 Hepatobiliary Surgery, Wuzhou Peoples Hospital, 543001 - Wuzhou/CN
  • 5 Hepatobiliary Surgery, Guangxi Medical University Cancer Hospital, 530021 - nanning/CN
  • 6 Pathology, Guangxi Medical University Cancer Hospital, 530021 - nanning/CN

Resources

This content is available to ESMO members and event participants.

Abstract 213P

Background

Adjuvant immune checkpoint inhibitors (ICIs) in patients with hepatocellular carcinoma (HCC) may improve recurrence-free survival (RFS). This study aims to compare the effects of different treatment duration of ICIs on RFS and overall survival (OS).

Methods

Between January 1, 2019 and January 1, 2024, the RFS and OS of HCC patients from three centers who received adjuvant ICIs therapy were compared with those who received active surveillance after curative resection. Further analysis was performed according to the different treatment duration of ICIs.

Results

Of the 1271 patients in the final analysis, 1032 (81.2%) received active surveillance, 239 (18.8%) received adjuvant ICIs therapy. The median RFS in the adjuvant therapy cohort was 22.6 months (95% CI: 18.3-26.9), significantly longer than that of 19.1 months (95% CI: 16.4-21.4) in the active surveillance cohort (HR 0.79, 95%CI 0.66-0.95, p=0.019). The median OS was not reached for either group, but the adjuvant therapy cohort exhibited a substantial advantage (HR 0.72, 95%CI 0.54-0.94; p=0.010). Similar results were obtained after propensity score matching. Patients who received more than 6 months duration of adjuvant ICI therapy had slightly higher RFS (HR 0.66, 95%CI 0.42-1.04; p=0.071) or OS (HR 0.59, 95%CI 0.30-1.17; p=0.128) than those who received up to 6 months.

Conclusions

Adjuvant ICIs therapy significantly improve the prognoses of patients with HCC at high risk of recurrence after curative resection. A duration of six months of adjuvant ICIs treatment might be sufficient.

Clinical trial identification

NCT05221398.

Editorial acknowledgement

Legal entity responsible for the study

The Ethics Committee of Guangxi Medical University Cancer Hospital.

Funding

This work was supported by the Specific Research Project of Guangxi for Research Bases and Talents (GuiKe AD22035057), Guangxi Key Research and Development Plan Project (GuiKe AB24010082), First-class Discipline Innovation-Driven Talent Program of Guangxi Medical University.

Disclosure

All authors have declared no conflicts of interest.

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