RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Characterizing immune profiles in hepatocellular carcinoma patients benefiting from pembrolizumab and lenvatinib using machine learning.
Characterizing immune profiles in hepatocellular carcinoma patients benefiting from pembrolizumab and lenvatinib using machine learning.
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本研究识别了接受 PL 治疗的 uHCC 患者中,有和无肿瘤缓解者之间不同的 ICPs,并确定了关键的免疫亚群。这些发现为在开始联合免疫治疗前开发临床结局预测工具提供了基础。
联合免疫疗法,如pembrolizumab联合lenvatinib(PL),常用于不可切除肝细胞癌(uHCC)的治疗。然而,预测哪些患者将从该疗法中获益仍具挑战性。本研究旨在通过比较PL治疗后达到客观缓解的uHCC患者(缓解者,R)与肿瘤进展患者(非缓解者,NR)之间的免疫细胞谱(ICP),并确定ICP的关键贡献因素,以解决这一问题。
我们在2019年7月至2023年7月期间前瞻性入组了51例uHCC患者。在开始PL治疗前采集外周血样本,并根据RECIST 1.1标准按肿瘤缓解情况分析ICPs。利用基线ICP数据开发了一个机器学习(ML)模型,以区分R与NR。
16例患者实现了客观肿瘤缓解,而11例在PL治疗后出现疾病进展。缓解者表现出更高水平的总T细胞、CD8 T细胞,以及CD4 T细胞、CD8 T细胞和NK细胞中PD-1+亚群。相比之下,NR具有更高比例的PD-L1+单核细胞。基于ICP训练的ML模型准确区分了两组,达到100%灵敏度和66.7%特异度,其中CD8 T细胞、PD-1+ CD8 NK细胞和PD-L1+单核细胞对分类贡献显著。
Combination immunotherapies, such as pembrolizumab plus lenvatinib (PL), are commonly used in treatment for unresectable hepatocellular carcinoma (uHCC). However, it remains challenging to predict which patients will benefit from this therapy. This study aimed to address this issue by comparing immune cell profiles (ICPs) between uHCC patients with objective response (responders, R) and those with tumor progression (non-responders, NR) following PL therapy, and to identify the key contributors to ICPs.
We prospectively enrolled 51 uHCC patients between July 2019 and July 2023. Peripheral blood samples were collected prior to initiating PL therapy, and ICPs were analyzed according to tumor response according to RECIST 1.1 criteria. A machine learning (ML) model was developed to differentiate R from NR using baseline ICP data.
16 patients achieved objective tumor responses, while 11 experienced disease progression following PL therapy. Responders exhibited higher levels of total T cells, CD8 T cells, and PD-1 + subpopulations of CD4 T cells, CD8 T cells, and NK cells. In contrast, NR had higher proportions of PD-L1 + monocytes. The trained ICP-based ML model accurately discriminated between the two groups, achieving 100% sensitivity and 66.7% specificity, with CD8 T cells, PD-1 + CD8 NK cells, and PD-L1 + monocytes contributing significantly to the classification.
This study recognized distinct ICPs between uHCC patients with and without tumor response to PL therapy and identified key contributing immune subpopulations. These findings provide a foundation for developing predictive tools for clinical outcomes before initiating combination immunotherapy.
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