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Genomic biomarkers to predict response to atezolizumab plus bevacizumab immunotherapy in hepatocellular carcinoma: Insights from the IMbrave150 trial

Authors
 Sun Young Yim  ;  Sung Hwan Lee  ;  Seung-Woo Baek  ;  Bohwa Sohn  ;  Yun Seong Jeong  ;  Sang-Hee Kang 5, Kena Park  ;  Hyewon Park  ;  Sunyoung S Lee  ;  Ahmed O Kaseb  ;  Young Nyun Park  ;  Sun-Hee Leem  ;  Michael A Curran  ;  Ji Hoon Kim  ;  Ju-Seog Lee 
Citation
 CLINICAL AND MOLECULAR HEPATOLOGY, Vol.30(4) : 807-823, 2024-10 
Journal Title
CLINICAL AND MOLECULAR HEPATOLOGY
ISSN
 2287-2728 
Issue Date
2024-10
MeSH
Aged ; Antibodies, Monoclonal, Humanized* / therapeutic use ; Antineoplastic Combined Chemotherapy Protocols* / therapeutic use ; Bevacizumab* / therapeutic use ; Biomarkers, Tumor* / genetics ; Biomarkers, Tumor* / metabolism ; Carcinoma, Hepatocellular* / drug therapy ; Carcinoma, Hepatocellular* / genetics ; Carcinoma, Hepatocellular* / pathology ; Carcinoma, Hepatocellular* / therapy ; Female ; Humans ; Immunotherapy ; Liver Neoplasms* / drug therapy ; Liver Neoplasms* / pathology ; Liver Neoplasms* / therapy ; Male ; Middle Aged ; Nivolumab / therapeutic use ; Sorafenib / therapeutic use
Keywords
Atezolizumab ; Bevacizumab ; Hepatocellular carcinoma ; Immunotherapy ; Transcriptome
Abstract
Background/aims: Combination immunotherapy, exemplified by atezolizumab plus bevacizumab, has become the standard of care for inoperable hepatocellular carcinoma (HCC). However, the lack of predictive biomarkers and limited understanding of response mechanisms remain a challenge.

Methods: Using data from the IMbrave150plus cohort, we applied an immune signature score (ISS) predictor to stratify HCC patients treated with atezolizumab plus bevacizumab or with sorafenib alone into potential high and low response groups. By applying multiple statistical approaches including a Bayesian covariate prediction algorithm, we refined the signature to 10 key genes (ISS10) for clinical use while maintaining similar predictive power to the full model. We further validated ISS10 in an independent HCC cohort treated with nivolumab plus ipilimumab.

Results: The study identified a significant association between the ISS and treatment response. Among patients classified as high responders, those treated with the atezolizumab plus bevacizumab combination exhibited improved overall and progression-free survival as well as better objective response rate compared to those treated with sorafenib. We also observed a significant correlation between ISS10 and response to nivolumab plus ipilimumab treatment. Analysis of immune cell subpopulations revealed distinct characteristics associated with ISS subtypes. In particular, the ISS10 high subtype displayed a more favorable immune environment with higher proportions of antitumor macrophages and activated T-cells, potentially explaining its better response.

Conclusion: Our study suggests that ISS and ISS10 are promising predictive biomarkers for enhanced therapeutic outcomes in HCC patients undergoing combination immunotherapy. These markers are crucial for refining patient stratification and personalized treatment approaches to advance the effectiveness of standard-of-care regimens.
Files in This Item:
T992024700.pdf Download
DOI
10.3350/CMH.2024.0333
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
Yonsei Authors
Park, Young Nyun(박영년) ORCID logo https://orcid.org/0000-0003-0357-7967
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/202320
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