Ye Bicheng, Fan Jun, Xue Lei, Zhuang Yu, Luo Peng, Jiang Aimin, Xie Jiaheng, Li Qifan, Liang Xiaoqing, Tan Jiaxiong, Zhao Songyun, Zhou Wenhang, Ren Chuanli, Lin Haoran, Zhang Pengpeng
Liver Disease Center of Integrated Traditional Chinese and Western Medicine, Department of Radiology, Zhongda Hospital, Medical School Southeast University, Nurturing Center of Jiangsu Province for State Laboratory of AI Imaging & Interventional Radiology (Southeast University) Nanjing China.
Department of Thoracic Surgery The First Affiliated Hospital of Nanjing Medical University Nanjing China.
Imeta. 2025 Mar 8;4(2):e70011. doi: 10.1002/imt2.70011. eCollection 2025 Apr.
To address the substantial variability in immune checkpoint blockade (ICB) therapy effectiveness, we developed an innovative R package called integrated Machine Learning and Genetic Algorithm-driven Multiomics analysis (iMLGAM), which establishes a comprehensive scoring system for predicting treatment outcomes through advanced multi-omics data integration. Our research demonstrates that iMLGAM scores exhibit superior predictive performance across independent cohorts, with lower scores correlating significantly with enhanced therapeutic responses and outperforming existing clinical biomarkers. Detailed analysis revealed that tumors with low iMLGAM scores display distinctive immune microenvironment characteristics, including increased immune cell infiltration and amplified antitumor immune responses. Critically, through clustered regularly interspaced short palindromic repeats screening, we identified Centrosomal Protein 55 () as a key molecule modulating tumor immune evasion, mechanistically confirming its role in regulating T cell-mediated antitumor immune responses. These findings not only validate iMLGAM as a powerful prognostic tool but also propose as a promising therapeutic target, offering novel strategies to enhance ICB treatment efficacy. The iMLGAM package is freely available on GitHub (https://github.com/Yelab1994/iMLGAM), providing researchers with an innovative approach to personalized cancer immunotherapy prediction.
为了解决免疫检查点阻断(ICB)治疗效果的巨大差异,我们开发了一种名为集成机器学习和遗传算法驱动的多组学分析(iMLGAM)的创新R包,它通过先进的多组学数据整合建立了一个用于预测治疗结果的综合评分系统。我们的研究表明,iMLGAM评分在独立队列中表现出卓越的预测性能,较低的分数与增强的治疗反应显著相关,并且优于现有的临床生物标志物。详细分析显示,iMLGAM评分低的肿瘤表现出独特的免疫微环境特征,包括免疫细胞浸润增加和抗肿瘤免疫反应增强。至关重要的是,通过成簇规律间隔短回文重复序列筛选,我们确定中心体蛋白55()是调节肿瘤免疫逃逸的关键分子,从机制上证实了其在调节T细胞介导的抗肿瘤免疫反应中的作用。这些发现不仅验证了iMLGAM作为一种强大的预后工具,还提出作为一个有前景的治疗靶点,为提高ICB治疗疗效提供了新策略。iMLGAM包可在GitHub(https://github.com/Yelab1994/iMLGAM)上免费获取,为研究人员提供了一种创新的个性化癌症免疫治疗预测方法。