CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Performance of Machine Learning Models Based on Medical Imaging in Predicting the expression of PD-L1 and CD8+TILs in Thoracic cancer: A Systematic Review and Meta-Analysis.
Performance of Machine Learning Models Based on Medical Imaging in Predicting the expression of PD-L1 and CD8+TILs in Thoracic cancer: A Systematic Review and Meta-Analysis.
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AI 驱动的医学影像对胸部肿瘤 TIME 展现出较强的预测能力,尤其是在 PD-L1 表达和 CD8+ TIL 预测方面。然而,显著的硏究间异质性限制了当前模型的普适性。未来研究应优先开展多中心、大规模研究,标准化影像特征提取,并整合生物学机制,以提高 AI 模型的临床适用性。
遵循PRISMA指南,我们系统检索了PubMed、Cochrane、Embase和Web of Science,检索截至2025年7月1日发表的研究。纳入评估AI驱动的医学影像用于预测胸部肿瘤TIME的研究。提取诊断准确性数据,并采用随机效应模型进行meta分析,以评估AI模型对PD-L1表达和CD8+ TILs的预测性能。同时进行了异质性分析和发表偏倚评估。
共纳入68项研究,其中25项符合meta分析条件。AI驱动的医学影像预测PD-L1表达的合并AUC为0.81(95% CI:0.78-0.85),敏感性为0.77(95% CI:0.74-0.80),特异性为0.73(95% CI:0.71-0.76)。对于CD8+ TIL预测,合并AUC为0.86(95% CI:0.82-0.89),敏感性为0.81(95% CI:0.72-0.87),特异性为0.81(95% CI:0.76-0.84)。亚组分析表明,整合多模态成像和深度学习模型可提高预测性能。然而,研究间存在显著异质性(I > 75%)。
Following PRISMA guidelines, we systematically searched PubMed, Cochrane, Embase, and Web of Science for studies published up to July 01, 2025. Studies evaluating AI-driven medical imaging for predicting thoracic tumor TIME were included. Diagnostic accuracy data were extracted, and a meta-analysis was conducted using a random-effects model to assess the predictive performance of AI models for PD-L1 expression and CD8+ TILs. Heterogeneity analysis and publication bias assessment were also performed.
A total of 68 studies were included, of which 25 were eligible for meta-analysis. The pooled area under the curve (AUC) for AI-driven medical imaging prediction of PD-L1 expression was 0.81 (95% CI: 0.78-0.85), with a sensitivity of 0.77 (95% CI: 0.74-0.80) and a specificity of 0.73 (95% CI: 0.71-0.76). For CD8+ TIL prediction, the pooled AUC was 0.86 (95% CI: 0.82-0.89), with a sensitivity of 0.81 (95% CI: 0.72-0.87) and a specificity of 0.81 (95% CI: 0.76-0.84). Subgroup analysis indicated that integrating multimodal imaging and deep learning models improved predictive performance. Nevertheless, considerable heterogeneity was observed among studies (I > 75%).
AI-driven medical imaging exhibits strong predictive capability for thoracic tumor TIME, particularly in PD-L1 expression and CD8+ TIL prediction. However, significant interstudy heterogeneity limits the generalizability of current models. Future studies should prioritize multicenter, large-scale research, standardization of imaging feature extraction, and integration of biological mechanisms to improve the clinical applicability of AI models.
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