Abstract 6874: A transcriptome-based AI meta-model for immunotherapy response classification in hepatocellular carcinoma.

Abstract Immune checkpoint inhibitor (ICI) is frequently selected as first-line therapy in advanced hepatocellular carcinoma (HCC), yet current biomarkers that predict therapeutic response show limited accuracy. Robust and clinically applicable predictors of ICI response in HCC need to be established. We performed tissue RNA-seq on ICI-treated HCC patients (Atezolizumab plus Bevacizumab, Nivolumab, or Ipilimumab plus Nivolumab) and developed an AI stacking-based meta-model to classify responders (R, n=32) and non-responders (NR, n=57). To address class imbalance, 80% of samples were distributed into three balanced training sets, and the remaining 20% were used as an internal test set. Gene-feature selection performed with six tree-based algorithms (AB, ERT, GB, LGB, RF, and XGB) improved mean AUC from 0.58 to 0.73 and mean MCC from 0.25 to 0.43. The stacking meta-model, incorporating 14 algorithms (AB, CB, ERT, GB, LGB, RF, XGB, four SVM kernels, LR, NB, and MLP), further increased mean AUC to 0.95 and MCC to 0.79. The meta-model achieved an AUC of 0.92 and MCC of 0.62 in the internal test set, and an AUC of 0.84 and MCC of 0.82 in an external ICI-treated HCC cohort (Table 1). Meta-scores derived from the model clearly stratified clinical outcomes. Patients with high scores showed improved PFS (HR 0.27, 95% CI 0.17-0.45; p<0.0001) and OS (HR 0.37, 95% CI 0.22-0.62; p<0.0001). Feature selection identified 11 AI-important gene (AIG) sets (10-173 genes each), and each set overlapped with at least two others through shared AIGs, reflecting convergent biological signals. Analysis of AIG sets in immune-cell populations from an external single-cell RNA-seq cohort revealed enrichment patterns consistent with known mechanisms of immune activation and resistance. These findings demonstrate that the AI meta-model can help to classify immunotherapy response in HCC and stratify survival outcomes, while revealing biologically relevant AIG signatures. Citation Format: Jimin Seo, Na Young Kwon, Ki Wook Lee, Han-En Lo, Young-Jun Jeon, . A transcriptome-based AI meta-model for immunotherapy response classification in hepatocellular carcinoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6874.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-6874
Primary Topic
Ferroptosis and cancer prognosis
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article
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article

Abstract 6874: A transcriptome-based AI meta-model for immunotherapy response classification in hepatocellular carcinoma.

Young-Jun Jeon, H.‐Y. Lo, Ki Wook Lee, Na Young Kwon et al.
Cancer Research
Ferroptosis and cancer prognosis
article

Abstract 6874: A transcriptome-based AI meta-model for immunotherapy response classification in hepatocellular carcinoma.

Young-Jun Jeon, H.‐Y. Lo, Ki Wook Lee, Na Young Kwon, Jimin Seo
article en

Abstract

Abstract Immune checkpoint inhibitor (ICI) is frequently selected as first-line therapy in advanced hepatocellular carcinoma (HCC), yet current biomarkers that predict therapeutic response show limited accuracy. Robust and clinically applicable predictors of ICI response in HCC need to be established. We performed tissue RNA-seq on ICI-treated HCC patients (Atezolizumab plus Bevacizumab, Nivolumab, or Ipilimumab plus Nivolumab) and developed an AI stacking-based meta-model to classify responders (R, n=32) and non-responders (NR, n=57). To address class imbalance, 80% of samples were distributed into three balanced training sets, and the remaining 20% were used as an internal test set. Gene-feature selection performed with six tree-based algorithms (AB, ERT, GB, LGB, RF, and XGB) improved mean AUC from 0.58 to 0.73 and mean MCC from 0.25 to 0.43. The stacking meta-model, incorporating 14 algorithms (AB, CB, ERT, GB, LGB, RF, XGB, four SVM kernels, LR, NB, and MLP), further increased mean AUC to 0.95 and MCC to 0.79. The meta-model achieved an AUC of 0.92 and MCC of 0.62 in the internal test set, and an AUC of 0.84 and MCC of 0.82 in an external ICI-treated HCC cohort (Table 1). Meta-scores derived from the model clearly stratified clinical outcomes. Patients with high scores showed improved PFS (HR 0.27, 95% CI 0.17-0.45; p<0.0001) and OS (HR 0.37, 95% CI 0.22-0.62; p<0.0001). Feature selection identified 11 AI-important gene (AIG) sets (10-173 genes each), and each set overlapped with at least two others through shared AIGs, reflecting convergent biological signals. Analysis of AIG sets in immune-cell populations from an external single-cell RNA-seq cohort revealed enrichment patterns consistent with known mechanisms of immune activation and resistance. These findings demonstrate that the AI meta-model can help to classify immunotherapy response in HCC and stratify survival outcomes, while revealing biologically relevant AIG signatures. Citation Format: Jimin Seo, Na Young Kwon, Ki Wook Lee, Han-En Lo, Young-Jun Jeon, . A transcriptome-based AI meta-model for immunotherapy response classification in hepatocellular carcinoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6874.

Cancer ResearchVol. 86(7_Supplement)
Sungkyunkwan University (KR)
Good health and well-being
Openalex Percentile: Top 5%
Ferroptosis and cancer prognosis
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