Kim Sanghee
College of Nursing, Keimyung University, Daegu, Republic of Korea.
Research (Wash D C). 2025 Aug 5;8:0795. doi: 10.34133/research.0795. eCollection 2025.
Chemotherapy-induced peripheral neuropathy (CIPN) is a common and debilitating adverse effect of cancer treatment that substantially impairs patients' quality of life and may lead to dose reduction or treatment discontinuation. Traditional prediction models based on single-modal data have shown limited accuracy in clinical settings. This study aimed to develop and evaluate a deep learning-based predictive model for CIPN by integrating multimodal data, including clinical, genomic, biosignal, wearable device, and imaging information. A retrospective and prospective cohort of cancer patients receiving chemotherapy between 2020 and 2025 was analyzed using data collected from multicenter electronic health records (EHRs) and public databases. An intermediate fusion framework was implemented using a Transformer-based architecture, which was compared with LSTM, CNN, and XGBoost models. SHAP (Shapley additive explanations) and Grad-CAM were used to improve model interpretability, while performance was assessed using AUC-ROC (area under the receiver operating characteristic curve), accuracy, sensitivity, specificity, and F1-score. The Transformer-based model achieved the highest performance (AUC = 0.93; accuracy = 88.5%; sensitivity = 85.3%; specificity = 90.1%), outperforming conventional models. SHAP analysis identified chemotherapy dosage, nerve magnetic resonance imaging abnormalities, electrocardiogram changes, CYP2C8 mutations, and diabetes as the most influential predictors. Patients with a high predicted risk of CIPN also demonstrated significantly lower overall survival, indicating a broader systemic impact of CIPN beyond neurological symptoms. This study provides evidence that deep learning models incorporating multimodal data significantly enhance CIPN prediction and have the potential for clinical implementation. The use of explainable artificial intelligence techniques further supports their integration into precision oncology. Future research should focus on multicenter validation, real-time EHR integration, and the development of neuroprotective strategies for high-risk patients.
化疗引起的周围神经病变(CIPN)是癌症治疗中一种常见且使人衰弱的副作用,会严重损害患者的生活质量,并可能导致剂量减少或治疗中断。基于单模态数据的传统预测模型在临床环境中的准确性有限。本研究旨在通过整合多模态数据(包括临床、基因组、生物信号、可穿戴设备和影像信息)来开发和评估一种基于深度学习的CIPN预测模型。使用从多中心电子健康记录(EHR)和公共数据库收集的数据,对2020年至2025年间接受化疗的癌症患者的回顾性和前瞻性队列进行了分析。使用基于Transformer的架构实现了一个中间融合框架,并将其与长短期记忆网络(LSTM)、卷积神经网络(CNN)和极端梯度提升(XGBoost)模型进行比较。使用SHAP(Shapley值加法解释)和梯度加权类激活映射(Grad-CAM)来提高模型的可解释性,同时使用受试者操作特征曲线下面积(AUC-ROC)、准确率、灵敏度、特异性和F1分数来评估性能。基于Transformer的模型表现出最高的性能(AUC = 0.93;准确率 = 88.5%;灵敏度 = 85.3%;特异性 = 90.1%),优于传统模型。SHAP分析确定化疗剂量、神经磁共振成像异常、心电图变化、细胞色素P450 2C8(CYP2C8)突变和糖尿病是最具影响力的预测因素。CIPN预测风险高的患者总体生存率也显著较低,这表明CIPN除了神经症状外还具有更广泛的全身影响。本研究提供了证据,表明整合多模态数据的深度学习模型显著增强了CIPN预测能力,并具有临床应用潜力。可解释人工智能技术的使用进一步支持了它们融入精准肿瘤学。未来的研究应侧重于多中心验证、实时EHR整合以及为高危患者开发神经保护策略。