4.6 Article

Artificial intelligence-based immunoprofiling serves as a potentially predictive biomarker of nivolumab treatment for advanced hepatocellular carcinoma

Journal

FRONTIERS IN MEDICINE
Volume 9, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fmed.2022.1008855

Keywords

hepatocellular carcinoma (HCC); immunoprofiling; predictive biomarker; nivolumab (PubChem SID; 178103907); immunotherapy; artificial intelligence

Funding

  1. FullHope Biomedical Co. Ltd.

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This study aimed to evaluate whether analyzing peripheral immune cell subsets using Mann-Whitney U test and artificial intelligence (AI) algorithms can predict the response to nivolumab treatment in advanced hepatocellular carcinoma (aHCC) patients. The results showed that this method could successfully separate disease control group from disease progression group, and PD-L1(+) monocytes and PD-L1(+) CD8 T cells played a significant role in this discrimination.
Immune checkpoint inhibitors (ICI) have been applied in treating advanced hepatocellular carcinoma (aHCC) patients, but few patients exhibit stable and lasting responses. Moreover, identifying aHCC patients suitable for ICI treatment is still challenged. This study aimed to evaluate whether dissecting peripheral immune cell subsets by Mann-Whitney U test and artificial intelligence (AI) algorithms could serve as predictive biomarkers of nivolumab treatment for aHCC. Disease control group carried significantly increased percentages of PD-L1(+) monocytes, PD-L1(+) CD8 T cells, PD-L1(+) CD8 NKT cells, and decreased percentages of PD-L1(+) CD8 NKT cells via Mann-Whitney U test. By recursive feature elimination method, five featured subsets (CD4 NKTreg, PD-1(+) CD8 T cells, PD-1(+) CD8 NKT cells, PD-L1(+) CD8 T cells and PD-L1(+) monocytes) were selected for AI training. The featured subsets were highly overlapping with ones identified via Mann-Whitney U test. Trained AI algorithms committed valuable AUC from 0.8417 to 0.875 to significantly separate disease control group from disease progression group, and SHAP value ranking also revealed PD-L1(+) monocytes and PD-L1(+) CD8 T cells exclusively and significantly contributed to this discrimination. In summary, the current study demonstrated that integrally analyzing immune cell profiling with AI algorithms could serve as predictive biomarkers of ICI treatment.

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