用深度学习方法评估口腔潜在恶性疾病的可检测性:一项回顾性试点研究。

Gaye Keser, Hakan Yülek, İbrahim Şevki Bayrakdar, Filiz Namdar Pekiner, Özer Çelik
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引用次数: 0

摘要

口腔潜在恶性疾病(OPMD)可能出现在口腔黏膜的恶性转化过程中,与正常组织相比,这些病变的细胞变化增加了癌症发展的可能性。本研究旨在评估一种基于深度学习的诊断软件的性能,该软件旨在检测OPMD。共使用358张经组织病理学诊断为口腔扁平苔藓、口腔白斑或口腔癌的患者的匿名回顾性口内图像。使用CranioCatch软件(CranioCatch, eski ehir, Turkey)中的多边形标记方法对图像进行注释,并由口腔、牙科和颌面放射科医师进行审查。数据集被分为训练集(n = 288)、验证集(n = 35)和测试集(n = 35)。开发了基于YOLOv8架构的深度学习模型,并使用混淆矩阵对其性能进行了评估。该模型的F1得分为0.693,灵敏度为0.666,精度为0.723。这些发现表明,深度学习和人工智能在OPMD的诊断中显示出希望,并且常规口腔检查和早期发现这些病变-特别是在高危人群中-是牙科专业人员的基本责任。临床翻译需要更大的、多中心的数据集、校准和外部验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of the Detectability of Oral Potentially Malignant Diseases with a Deep Learning Approach: A Retrospective Pilot Study.

Oral potentially malignant diseases (OPMD) may arise during the malignant transformation of the oral mucosa, with cellular changes in these lesions increasing the likelihood of cancer development compared to normal tissues. This study aims to evaluate the performance of a deep learning-based diagnostic software designed to detect OPMD. A total of 358 anonymized retrospective intraoral images from patients histopathologically diagnosed with oral lichen planus, oral leukoplakia, or oral cancer via incisional biopsy were used. The images were annotated using the polygonal labeling method in CranioCatch software (CranioCatch, Eskişehir, Turkey) and reviewed by Oral, Dental, and Maxillofacial Radiologists. The dataset was divided into training (n = 288), validation (n = 35), and test (n = 35) sets. A deep learning model based on the YOLOv8 architecture was developed, and its performance was assessed using a confusion matrix. The model achieved an F1 score of 0.693, a sensitivity of 0.666, and a precision of 0.723. These findings suggest that deep learning and artificial intelligence show promise in the diagnosis of OPMD and that routine oral examinations and early detection of these lesions-especially in high-risk individuals-are essential responsibilities for dental professionals. Larger, multi-center datasets, calibration, and external validation are needed for clinical translation.

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