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

IF 14 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Clinical and Molecular Hepatology Pub Date : 2024-10-01 Epub Date: 2024-07-23 DOI:10.3350/cmh.2024.0333
Sun Young Yim, Sung Hwan Lee, Seung-Woo Baek, Bohwa Sohn, Yun Seong Jeong, Sang-Hee Kang, 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
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引用次数: 0

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.

预测肝细胞癌患者对Atezolizumab加贝伐单抗免疫疗法反应的基因组生物标志物:IMbrave150试验的启示。
简介以阿特珠单抗加贝伐单抗为代表的联合免疫疗法已成为治疗无法手术的肝细胞癌(HCC)的标准疗法。然而,缺乏预测性生物标志物和对反应机制的了解有限仍然是一个挑战:利用 IMbrave150plus 队列的数据,我们应用免疫特征评分(ISS)预测因子将接受阿特珠单抗加贝伐单抗治疗或单用索拉非尼治疗的 HCC 患者分为潜在的高反应组和低反应组。通过应用包括贝叶斯协变量预测算法在内的多种统计方法,我们将特征细化为 10 个关键基因(ISS10),供临床使用,同时保持了与完整模型相似的预测能力。我们在使用尼妥珠单抗加伊匹单抗治疗的独立HCC队列中进一步验证了ISS10:结果:研究发现 ISS 与治疗反应之间存在显著关联。在被归类为高反应者的患者中,与索拉非尼治疗的患者相比,阿特珠单抗加贝伐单抗联合治疗的患者总生存期和无进展生存期得到改善,客观反应率也更高。我们还观察到ISS10与nivolumab加伊匹单抗治疗反应之间存在明显的相关性。对免疫细胞亚群的分析显示了与ISS亚型相关的不同特征。特别是,ISS10高亚型显示出更有利的免疫环境,抗肿瘤巨噬细胞和活化T细胞比例更高,这可能是其反应更好的原因:我们的研究表明,ISS和ISS10是有希望提高接受联合免疫疗法的HCC患者治疗效果的预测性生物标志物。这些标志物对于完善患者分层和个性化治疗方法以提高标准治疗方案的有效性至关重要。
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来源期刊
Clinical and Molecular Hepatology
Clinical and Molecular Hepatology Medicine-Hepatology
CiteScore
15.60
自引率
9.00%
发文量
89
审稿时长
10 weeks
期刊介绍: Clinical and Molecular Hepatology is an internationally recognized, peer-reviewed, open-access journal published quarterly in English. Its mission is to disseminate cutting-edge knowledge, trends, and insights into hepatobiliary diseases, fostering an inclusive academic platform for robust debate and discussion among clinical practitioners, translational researchers, and basic scientists. With a multidisciplinary approach, the journal strives to enhance public health, particularly in the resource-limited Asia-Pacific region, which faces significant challenges such as high prevalence of B viral infection and hepatocellular carcinoma. Furthermore, Clinical and Molecular Hepatology prioritizes epidemiological studies of hepatobiliary diseases across diverse regions including East Asia, North Asia, Southeast Asia, Central Asia, South Asia, Southwest Asia, Pacific, Africa, Central Europe, Eastern Europe, Central America, and South America. The journal publishes a wide range of content, including original research papers, meta-analyses, letters to the editor, case reports, reviews, guidelines, editorials, and liver images and pathology, encompassing all facets of hepatology.
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