PO.BCS02.04 · 生物信息与计算

使用普遍可及、跨平台、AI驱动的应用程序进行肺癌智能检测(LUCID)

Lung cancer intelligent detection (LUCID) using a universally accessible, cross-platform, AI-powered application

海报缩略图:使用普遍可及、跨平台、AI驱动的应用程序进行肺癌智能检测(LUCID)
编号 2783 展板 14 时间 4/20 02:00–05:00 区域 Section 4 主讲 Gowrishankar Palaniswamy, MBBS
分会场 Radiomics and AI in Medical Imaging
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作者与单位 Authors & Affiliations

Gowrishankar Palaniswamy 1, Elangovan Krishnan2, Jansi R. Sethuraj3, Muhammad Waqas Khan4, Aravind Raghavan1

1MUSC Health Lancaster Medical Center, Medical University of South Carolina, Lancaster, SC,2AIM DOCTOR, Chennai, India,3The University of Texas Health Science Center at Houston, Houston, TX,4Medical University of South Carolina ( MUSC ), Lancaster, SC

摘要 Abstract

中文摘要
引言:肺癌是全球癌症相关死亡的首要原因。仅29%的患者实现5年生存,主要是由于诊断较晚。此外,其经济负担在国际上超过3.9万亿美元。所有肺癌患者中仅有三分之一被足够早地诊断,从而能够实施有效治疗。深度学习架构已彻底改变了诊断影像,能够提取超越人类能力的复杂影像模式。EfficientNetB0是一种最先进的卷积神经网络,实现了卓越的准确性和计算效率。其应用于计算机断层扫描(CT)影像为肺癌早期检测和降低死亡率提供了前所未有的潜力。 方法:将正常、良性和恶性肺(n = 1190)的匿名CT图像按比例分为训练集(60%)、验证集(20%)和测试集(20%)。预处理和增强提高了数据质量和模型泛化能力。对EfficientNetB0进行了训练和优化,在验证集和测试集上通过准确性、精确率-召回率、F1分数、F2分数和受试者工作特征曲线下面积(AUROC)评估性能。将训练好的模型部署在一个普遍可及、跨平台的应用程序中,供全球专家进行独立验证。 结果:EfficientNetB0在区分正常、良性和恶性肺病灶方面表现出卓越性能。该模型对两个类别均实现了完美的准确性、精确率和召回率,F1分数为1.00(训练和验证)。AUROC值为1.00,展示了出色的判别能力。混淆矩阵证实在137个病灶(24个良性、113个恶性)中零误分类。该模型的卓越性能表明其在增强临床决策和推进公平癌症护理方面具有巨大潜力。 结论:EfficientNetB0代表了CT影像上肺癌分层的范式转变诊断工具,展示了增强放射科专家解读的临床级准确性。该模型卓越的判别能力实现了高敏感性和特异性,使其成为常规诊断工作流程的变革性辅助工具。通过可及的跨平台应用程序进行部署有助于在资源受限环境中传播,使精准诊断民主化。这种深度学习架构大幅增强了早期检测能力,有可能通过及时的临床干预降低死亡率。这些发现为前瞻性验证研究和临床整合奠定了坚实基础,以优化全球肺癌结局。
查看英文原文 English abstract
Introduction: Lung cancer represents the leading cause of cancer-related mortality globally. Only 29% achieve 5-year survival, primarily due to late diagnoses. In addition, the economic burden exceeds $3.9 trillion internationally. Only one-third of all lung cancer patients are diagnosed early enough so that effective treatment can be implemented. Deep learning architectures have revolutionized diagnostic imaging, extracting complex imaging patterns beyond human capability. EfficientNetB0, a state-of-the-art convolutional neural network achieves remarkable accuracy and computational efficiency. Its application to computed tomography (CT) imaging offers unprecedented potential for early lung cancer detection and mortality reduction. Methods: Anonymized CT images of normal, benign, and malignant lung (n = 1190) were proportioned into training (60%), validation (20%), and testing (20%) sets. Preprocessing and augmentation improved data quality and model generalizability. EfficientNetB0 was trained and optimized, with performance evaluated by accuracy, precision-recall, F1-score, F2-score, and area under the receiver operating characteristic curve (AUROC) on validation and test sets. The trained model was deployed in a universally accessible, cross-platform application for independent validation by experts globally. Results: EfficientNetB0 demonstrated exceptional performance in distinguishing normal, benign, and malignant lung lesions. The model achieved perfect accuracy, precision, and recall for both classes, with F1-scores of 1.00 (training and validation). AUROC values of 1.00 demonstrate outstanding discriminative capacity. The confusion matrix confirmed zero misclassifications across 137 lesions (24 benign, 113 malignant). The model's exemplary performance suggests substantial potential to augment clinical decision-making and advance equitable cancer care. Conclusion: EfficientNetB0 represents a paradigm-shifting diagnostic tool for lung cancer stratification on CT imaging, demonstrating clinical-grade accuracy that augments expert radiologist interpretation. The model's exceptional discriminative capacity, achieving high sensitivity and specificity, positions it as a transformative adjunct to conventional diagnostic workflows. Deployment via an accessible cross-platform application facilitates dissemination across resource-constrained environments, democratizing precision diagnostics. This deep learning architecture substantially augments early detection capabilities, potentially reducing mortality through timely clinical intervention. These findings establish a robust foundation for prospective validation studies and clinical integration to optimize lung cancer outcomes globally.
利益披露 Disclosure
G. Palaniswamy , None.. J. R. Sethuraj, None.. A. Raghavan, None.

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