KMeansGraphMIL:用于预测结直肠癌肿瘤突变负担的弱监督多实例学习模型。

IF 4.7 2区 医学 Q1 PATHOLOGY
Linghao Chen, Huiling Xiao, Jiale Jiang, Bing Li, Weixiang Liu, Wensheng Huang
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引用次数: 0

摘要

结直肠癌(CRC)是全球三大最致命的恶性肿瘤之一,对人类健康构成重大威胁。最近提出的免疫治疗检查点阻断治疗已被证明对结直肠癌有效,但其使用取决于对患者特异性生物标志物的测量。在这些生物标志物中,肿瘤突变负荷(Tumor Mutational Burden, TMB)已成为一种新的指标,传统上需要新一代测序(NGS)来测量,这是耗时、劳动密集型和昂贵的。为了提供一种经济、快速的预测患者TMB的方法,我们提出了基于弱监督多实例学习(WSMIL)的KMeansGraphMIL模型。与以前的WSMIL模型相比,KMeansGraphMIL既利用了图像patch特征向量的相似性,又利用了patch之间的空间关系。该方法将模型的AUC提高到0.8334,并将召回率显著提高到0.7556。因此,我们提出了一个经济快速的预测CRC TMB的框架,为医生提供了快速制定治疗计划的潜力,为患者节省了大量的时间和金钱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
KMeansGraphMIL: A Weakly Supervised Multiple Instance Learning Model for Predicting Colorectal Cancer Tumor Mutational Burden.

Colorectal cancer (CRC) is one of the top three most lethal malignancies worldwide, posing a significant threat to human health. Recently proposed immunotherapy checkpoint blockade treatments have proven effective for CRC, but their use depends on measuring specific biomarkers in patients. Among these biomarkers, tumor mutational burden (TMB) has emerged as a novel indicator, traditionally requiring next-generation sequencing for measurement, which is time-consuming, labor intensive, and costly. To provide an economical and rapid way to predict patients' TMB, we propose the KMeansGraphMIL model based on weakly supervised multiple-instance learning. Compared with previous weakly supervised multiple-instance learning models, KMeansGraphMIL leverages both the similarity of image patch feature vectors and the spatial relationships between patches. This approach improves the model's area under the receiver operating characteristic curve to 0.8334 and significantly increases the recall to 0.7556. Thus, we present an economical and rapid framework for predicting CRC TMB, offering the potential for physicians to quickly develop treatment plans and saving patients substantial time and money.

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来源期刊
CiteScore
11.40
自引率
0.00%
发文量
178
审稿时长
30 days
期刊介绍: The American Journal of Pathology, official journal of the American Society for Investigative Pathology, published by Elsevier, Inc., seeks high-quality original research reports, reviews, and commentaries related to the molecular and cellular basis of disease. The editors will consider basic, translational, and clinical investigations that directly address mechanisms of pathogenesis or provide a foundation for future mechanistic inquiries. Examples of such foundational investigations include data mining, identification of biomarkers, molecular pathology, and discovery research. Foundational studies that incorporate deep learning and artificial intelligence are also welcome. High priority is given to studies of human disease and relevant experimental models using molecular, cellular, and organismal approaches.
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