Abstract 948P
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 ICIs drugs and treatment duration on RFS and overall survival (OS).
Methods
Between January 1, 2019 and December 1, 2023, the RFS and OS of patients from three centers who received adjuvant ICIs with or without molecular targeted therapy were compared with those who did not receive any antineoplastic therapy after curative resection. Subgroup analysis was further performed according to the type and treatment duration of ICIs. Propensity score matching (PSM) was used to reduce the bias caused by the imbalance of baseline variables.
Results
Of the 1171 patients in the final analysis, 932 (79.6%) received no adjuvant therapy, 126 (10.8%) received ICIs alone, and 113 (9.6%) received both adjuvant ICIs and molecular targeted agents. Patients with adjuvant ICIs treatment were with statistically significant RFS (HR 0.735, 95%CI 0.597-0.904) and OS (HR 0.472, 95%CI 0.334-0.668) than those with no adjuvant therapy. Similar results were obtained after PSM. Adjuvant tislelizumab, sintilimab, camrelizumab, and toripalimab were associated with similar RFS or OS. Moreover, patients who received less than six months duration of ICIs treatment had similar RFS or OS with those who received more than six months duration of ICIs treatment.
Conclusions
Adjuvant ICIs with or without TKIs can improve the prognosis of patients with HCC at high risk of recurrence after curative resection. There was no significant difference in efficacy among drugs. A duration of six months of adjuvant treatment may be sufficient.
Clinical trial identification
NCT05221398.
Editorial acknowledgement
Legal entity responsible for the study
Guangxi Medical University Cancer Hospital.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1407P - Pan-immune-inflammation value predicts the survival of patients with esophageal squamous cell carcinoma receiving immunotherapy and chemoradiotherapy: A pooled-analysis of two phase II trials
Presenter: Xingyuan Cheng
Session: Poster session 17
1408P - DVDMS (Sinoporphyrin sodium)-mediated photodynamic therapy (PDT) vs treatment of physician’s choice in patients with advanced esophageal cancer (EC): Preliminary results of DYNA-Esophagus03, a randomized, open-labeled, multicenter phase IIIb study
Presenter: Jun Zhou
Session: Poster session 17
1409P - Advancing esophageal cancer radiotherapy: AS-NeSt's 3D predictive proficiency for personalized dose distribution
Presenter: Yanhua Duan
Session: Poster session 17
Resources:
Abstract
1410P - Efficacy of fruquintinib plus paclitaxel (F+PTX) in patients (pts) with prior immunotherapy (prior-IO): Subgroup analysis from FRUTIGA study
Presenter: Lin Shen
Session: Poster session 17
1411P - AI-powered immune phenotype predicts favorable outcomes of nivolumab (niv) plus chemotherapy (chemo) in advanced fgastric cancer (AGC): A multi-center real-world data analysis
Presenter: Hyung-don Kim
Session: Poster session 17
1412P - Intestinal microbiota as a biological marker for pre-neoplastic lesion in gastric cancer in Amazonas, Brazil
Presenter: ÁBNER PAZ
Session: Poster session 17
Resources:
Abstract
1413P - Multi-modal deep-learning model for real-time prediction of recurrence in early-stage esophageal cancer: A multi-modal approach
Presenter: Hyun Ae Jung
Session: Poster session 17
1414P - Iparomlimab and tuvonralimab (QL1706) with definitive chemoradiotherapy for locally advanced esophageal squamous cell carcinoma: An open-label phase II study
Presenter: Wencheng Zhang
Session: Poster session 17
1415P - Real-world data on the use of nivolumab plus chemotherapy for patients with metastatic GC/GEJC/EAC: A Canadian perspective
Presenter: Mustapha Tehfe
Session: Poster session 17
1416P - First-line tislelizumab combined with bevacizumab and CAPOX for metastatic gastroesophageal adenocarcinoma (mGEA) with PD-L1 CPS<5: Updated results of a phase II, prospective, single-arm study
Presenter: guanghai dai
Session: Poster session 17