基于多模态深度学习的非小细胞肺癌免疫治疗反应预测和生物标志物发现。

IF 4.6 2区 医学 Q1 COMPUTER SCIENCE, INFORMATION SYSTEMS
Zijun Wang, Xi Liu, Kaitai Han, Lixin Lei, Chaojing Shi, Wu Liu, Qianjin Guo
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引用次数: 0

摘要

免疫疗法已成为晚期非小细胞肺癌(NSCLC)的一种有希望的治疗方法,但准确预测哪些患者将从中受益仍然是一个主要的临床挑战。为了解决这个问题,我们的目标是开发一种新的多模式方法,DeepAFM,该方法集成了组织病理学,基因组特征和临床信息,以预测患者对抗pd -(L)1免疫治疗的反应。材料和方法:本研究共纳入93例晚期NSCLC患者。组织病理学全片图像使用自监督VQVAE2进行表征学习处理。然后应用主成分分析和K-means聚类进行降维和特征分组。通过排列重要性评价和颜色编码技术对感兴趣的关键区域进行可视化。提取的组织病理学特征以及基因组改变和临床变量被整合到DeepAFM多模态预测模型中。结果:DeepAFM获得了较高的预测性能,曲线下面积(AUC)为0.77(95%置信区间:0.69-1.00)。基于注意力的热图显示,该模型可以识别与患者免疫治疗反应相关的关键病理模式、基因组突变和临床指标。讨论:多模态数据的整合使该模型能够捕获病理、基因组学和临床特征之间复杂的相互作用,增强免疫治疗反应预测的可解释性和预测能力。可视化技术有助于识别生物学上有意义的特征和潜在的生物标志物。结论:本研究证明了DeepAFM在预测晚期非小细胞肺癌免疫治疗应答方面的有效性。该方法不仅提高了预测的准确性,而且为个性化治疗策略和生物标志物的发现提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multimodal deep learning for immunotherapy response prediction and biomarker discovery in non-small cell lung cancer.

Objective: Immunotherapy has emerged as a promising treatment for advanced non-small cell lung cancer (NSCLC), but accurately predicting which patients will benefit from it remains a major clinical challenge. To address this, we aim to develop a novel multimodal method, DeepAFM, that integrates histopathology, genomic features, and clinical information to predict patient responses to anti-PD-(L)1 immunotherapy.

Materials and methods: A total of 93 patients with advanced NSCLC were included in this study. Histopathological whole-slide images were processed using a self-supervised VQVAE2 for representation learning. PCA and K-means clustering were then applied for dimensionality reduction and feature grouping. Key regions of interest were visualized through permutation importance evaluation and color-coding techniques. The extracted histopathological features, along with genomic alterations and clinical variables, were integrated into the DeepAFM multimodal prediction model.

Results: The DeepAFM achieved a high predictive performance with an area under the curve (AUC) of 0.77 (95% confidence interval: 0.69-1.00). Attention-based heatmaps revealed that the model could identify critical pathological patterns, genomic mutations, and clinical indicators associated with patient responses to immunotherapy.

Discussion: The integration of multimodal data enabled the model to capture complex interactions among pathology, genomics, and clinical characteristics, enhancing the interpretability and predictive power of immunotherapy response prediction. The visualization techniques facilitated the identification of biologically meaningful features and potential biomarkers.

Conclusion: This study demonstrates the effectiveness of the DeepAFM in predicting responses to immunotherapy in advanced NSCLC. The approach not only improves prediction accuracy but also provides valuable insights for personalized treatment strategies and biomarker discovery.

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来源期刊
Journal of the American Medical Informatics Association
Journal of the American Medical Informatics Association 医学-计算机:跨学科应用
CiteScore
14.50
自引率
7.80%
发文量
230
审稿时长
3-8 weeks
期刊介绍: JAMIA is AMIA''s premier peer-reviewed journal for biomedical and health informatics. Covering the full spectrum of activities in the field, JAMIA includes informatics articles in the areas of clinical care, clinical research, translational science, implementation science, imaging, education, consumer health, public health, and policy. JAMIA''s articles describe innovative informatics research and systems that help to advance biomedical science and to promote health. Case reports, perspectives and reviews also help readers stay connected with the most important informatics developments in implementation, policy and education.
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