CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Artificial intelligence in cancer immunotherapy: current trends in predicting response and personalizing treatment.
Artificial intelligence in cancer immunotherapy: current trends in predicting response and personalizing treatment.
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人工智能(AI)可通过更准确地预测治疗应答、发现特异性生物标志物和制定个体化治疗方案,改变癌症免疫治疗。传统单一标志物(PD-L1、TMB、MSI)在不同肿瘤类型中的表现不一致,也无法评估肿瘤异质性或动态肿瘤微环境(TME)。本综述总结多模态AI模型的进展:这些模型整合基因组学、转录组学、影像组学、数字病理学(病理组学)、循环生物标志物和临床证据,建立判别能力显著更强的综合预测特征。少数回顾性研究显示,基于全切片图像、CT/MRI/PET影像组学、空间和单细胞组学以及多组学融合的深度学习和集成模型AUC超过0.8;但前瞻性和多中心验证稀少,外部验证中模型表现常下降。
AI还用于改进过继细胞疗法(如CAR-T)的转化流程,包括患者选择、生产优化(如数字孪生)和早期毒性预测(如CRS、ICANS)。尽管前瞻性、多中心验证和可解释AI对于建立临床医生信任及监管认可至关重要,数据异质性、偏倚、纵向验证不足、可重复性有限以及多数模型缺乏透明度,仍妨碍临床实施。联邦学习、基础模型、空间组学、数字孪生和可穿戴设备监测等新系统,为构建可泛化、保护隐私且可在临床实践中采取行动的系统提供了路径。要实现AI潜力,必须标准化数据生成、确保报告透明、加强跨学科协作,并强化以AI实际应用和患者安全为重点的监管框架。通过这些措施,AI有望从回顾性研究工具转变为前瞻性临床决策支持工具,切实提升癌症免疫治疗的个体化水平和结局。
Artificial intelligence (AI) can transform cancer immunotherapy by enabling more accurate prediction of treatment responses, the discovery of specific biomarkers, and the development of personalised treatment plans. Traditional single-marker biomarkers (PD-L1, TMB, MSI) lack consistency across tumour types and cannot be used to assess tumour heterogeneity or the dynamic tumour microenvironment (TME). This review synthesises developments in multimodal AI models that combine genomics, transcriptomics, radiomics, digital pathology (pathomics), circulating biomarkers, and clinical evidence to create composite predictive signatures with significantly better discriminatory value. AUCs over 0. 8 have been seen in a few retrospective studies with deep learning and ensemble models on whole-slide images, CT/MRI/PET radiomics, spatial and single-cell omics, and multi-omics fusion models, but prospective and multicentre validation is scarce, and external validation often shows deterioration in performance. AI is also used to enhance the translational pipelines of adoptive cell therapies (e. g.
, CAR-T) by improving patient selection, manufacturing (e. g. , digital twins), and early toxicity prediction (e. g. , CRS, ICANS). Nevertheless, clinical implementation remains hindered by data heterogeneity, bias, poor longitudinal validation, limited reproducibility, and a lack of transparency in most models, even though prospective, multicenter validation and explainable AI are crucial for clinician trust and regulatory acceptance. New systems such as federated learning, foundation models, spatial omics, digital twins, and wearable monitoring represent paths to generalizable, privacy-preserving, and actionable systems in clinical practice.
To achieve the potential of AI, the generation of data will need to be standardized, reporting must be transparent, interdisciplinary, and regulatory frameworks must be strengthened focusing on the practical use of AI and patient safety. By taking these steps, AI could be shifted to prospective clinical decision support, which uses AI to meaningfully enhance personalization and outcomes in cancer immunotherapy based on a retrospective research tool.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
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