Development of an Artificial Intelligence System for Distinguishing Malignant from Benign Soft Tissue Tumors Using Contrast-Enhanced MR Images.

IF 2.5 3区 医学 Q3 ONCOLOGY Oncology Pub Date : 2024-10-23 DOI:10.1159/000542228
Toru Hirozane, Masahiro Hashimoto, Hasnine Haque, Yuki Arita, Tomoaki Mori, Naofumi Asano, Robert Nakayama, Takeshi Morii, Naobumi Hosogane, Morio Matsumoto, Masaya Nakamura, Masahiro Jinzaki
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Abstract

Introduction: The integration of artificial intelligence (AI) into orthopedics has enhanced the diagnosis of various conditions; however, its use in diagnosing soft-tissue tumors remains limited owing to its complexity. This study aimed to develop and assess an AI-driven diagnostic support system for magnetic resonance imaging (MRI)-based soft-tissue tumor diagnosis, potentially improving accuracy and aiding radiologists and orthopedic surgeons.

Methods: Experienced orthopedic oncologists and radiologists annotated 720 images from 77 cases (41 benign and 36 malignant soft-tissue tumors). Eleven tumor subtypes were identified and classified into benign and malignant groups based on histological diagnosis. Utilizing the standard machine learning classifier pipeline, we examined and down-selected imaging protocols and their predominant radiomic features within the tumor's three-dimensional region to differentiate between benign and malignant tumors. Among the scan protocols, contrast-enhanced T1 weighted fat-suppressed images showed the most accurate classification based on radiomics features. We focused on the two-dimensional features from the largest tumor boundary surface and its neighboring slices, leveraging texture-based radiomic and deep convolutional neural network features from a pretrained VGG19 model.

Results: The test data comprised 44 contrast-enhanced images (22 benign and 22 malignant soft-tissue tumors) containing six malignant and five benign subtypes distinct from the training data. We compared expert and non-expert human performances against AI by assessing malignancy detection and the time required for classification. The AI model showed comparable accuracy (AUC 0.91) to that of radiologists (AUC 0.83) and orthopedic surgeons (AUC 0.73). Notably, the AI model processed data approximately 400 times faster than its human counterparts, showcasing its capacity to significantly boost diagnostic efficiency.

Conclusion: We developed an AI-driven diagnostic support system for MRI-based soft-tissue tumor diagnosis. While additional refinement is necessary for clinical applications, our system has exhibited promising potential in differentiating between benign and malignant soft-tissue tumors based on MRI.

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开发人工智能系统,利用对比增强磁共振图像区分恶性和良性软组织肿瘤。
简介:人工智能(AI)与骨科的结合增强了对各种疾病的诊断能力:人工智能(AI)与骨科的结合提高了对各种疾病的诊断水平;然而,由于软组织肿瘤的复杂性,人工智能在诊断软组织肿瘤方面的应用仍然有限。本研究旨在开发和评估一种人工智能驱动的诊断支持系统,用于基于磁共振成像(MRI)的软组织肿瘤诊断,从而提高准确性,为放射科医生和骨科医生提供帮助:经验丰富的骨科肿瘤专家和放射科专家对 77 例病例(41 例良性软组织肿瘤和 36 例恶性软组织肿瘤)的 720 张图像进行了注释。根据组织学诊断确定了 11 种肿瘤亚型,并将其分为良性和恶性两组。利用标准的机器学习分类器管道,我们检查并向下选择了成像方案及其在肿瘤三维区域内的主要放射学特征,以区分良性和恶性肿瘤。在这些扫描方案中,对比增强 T1 加权脂肪抑制图像显示出最准确的放射学特征分类。我们重点研究了来自最大肿瘤边界表面及其邻近切片的二维特征,利用基于纹理的放射组学特征和来自预训练 VGG19 模型的深度卷积神经网络特征:测试数据包括 44 张对比度增强图像(22 张良性和 22 张恶性软组织肿瘤),其中包含与训练数据不同的 6 个恶性亚型和 5 个良性亚型。我们通过评估恶性肿瘤检测和分类所需时间,比较了专家和非专家人类与人工智能的表现。人工智能模型的准确率(AUC 0.91)与放射科医生(AUC 0.83)和骨科医生(AUC 0.73)相当。值得注意的是,人工智能模型处理数据的速度比人类同行快约 400 倍,这表明它有能力显著提高诊断效率:我们开发了一种人工智能驱动的诊断支持系统,用于基于核磁共振成像的软组织肿瘤诊断。虽然在临床应用中还需要进一步改进,但我们的系统在根据核磁共振成像区分良性和恶性软组织肿瘤方面表现出了巨大的潜力。
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来源期刊
Oncology
Oncology 医学-肿瘤学
CiteScore
6.00
自引率
2.90%
发文量
76
审稿时长
6-12 weeks
期刊介绍: Although laboratory and clinical cancer research need to be closely linked, observations at the basic level often remain removed from medical applications. This journal works to accelerate the translation of experimental results into the clinic, and back again into the laboratory for further investigation. The fundamental purpose of this effort is to advance clinically-relevant knowledge of cancer, and improve the outcome of prevention, diagnosis and treatment of malignant disease. The journal publishes significant clinical studies from cancer programs around the world, along with important translational laboratory findings, mini-reviews (invited and submitted) and in-depth discussions of evolving and controversial topics in the oncology arena. A unique feature of the journal is a new section which focuses on rapid peer-review and subsequent publication of short reports of phase 1 and phase 2 clinical cancer trials, with a goal of insuring that high-quality clinical cancer research quickly enters the public domain, regardless of the trial’s ultimate conclusions regarding efficacy or toxicity.
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