基于深度学习的弥漫性大b细胞淋巴瘤复发可解释性预测。

Hussein Naji, Paul Hahn, Juan I Pisula, Stefano Ugliano, Adrian Simon, Reinhard Büttner, Katarzyna Bozek
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引用次数: 0

摘要

背景:弥漫性大b细胞淋巴瘤(DLBCL)的异质性和侵袭性给治疗带来了重大挑战,高达50%的患者在化疗后复发。对复发患者的预先检测可以提供替代治疗。深度学习在预测各种癌症复发方面显示出潜力,但缺乏可解释性。特别是在预测复发方面,理解模型的决定可能最终导致新的治疗方法。方法:我们开发了一个基于深度学习的管道来预测DLBCL的复发,该管道基于一个公开的队列的组织学图像。我们利用基于注意力的分类来突出显示图像中与模型分类高度相关的区域。随后,我们对这些区域内的细胞核进行分割,计算形态学特征,并进行统计分析,发现复发和非复发患者之间的差异。结果:我们的f1得分为0.88,表明我们的模型可以区分非复发和复发患者。此外,我们发现最能预测复发的特征包括大且形状不规则的肿瘤细胞核。讨论:我们的工作强调了组织学图像在预测治疗结果方面的价值,并增强了我们对侵袭性异质癌症(如DLBCL)复杂生物学过程的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Deep learning-based interpretable prediction of recurrence of diffuse large B-cell lymphoma.

Background: The heterogeneous and aggressive nature of diffuse large B-cell lymphoma (DLBCL) presents significant treatment challenges as up to 50% of patients experience recurrence of disease after chemotherapy. Upfront detection of recurring patients could offer alternative treatments. Deep learning has shown potential in predicting recurrence of various cancer types but suffers from lack of interpretability. Particularly in prediction of recurrence, an understanding of the model's decision could eventually result in novel treatments.

Methods: We developed a deep learning-based pipeline to predict recurrence of DLBCL based on histological images of a publicly available cohort. We utilized attention-based classification to highlight areas within the images that were of high relevance for the model's classification. Subsequently, we segmented the nuclei within these areas, calculated morphological features, and statistically analyzed them to find differences between recurred and non-recurred patients.

Results: We achieved an f1 score of 0.88 indicating that our model can distinguish non-recurred from recurred patients. Additionally, we found that features that are the most predictive of recurrence include large and irregularly shaped tumor cell nuclei.

Discussion: Our work underlines the value of histological images in predicting treatment outcomes and enhances our understanding of complex biological processes in aggressive, heterogeneous cancers like DLBCL.

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