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深度形态学学习增强基于药物表型分析的体外精准医疗。

Deep Morphology Learning Enhances Ex Vivo Drug Profiling-Based Precision Medicine.

机构信息

Department of Biology, Institute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland.

Department of Pathology, Medical University of Vienna, Vienna, Austria.

出版信息

Blood Cancer Discov. 2022 Nov 2;3(6):502-515. doi: 10.1158/2643-3230.BCD-21-0219.

Abstract

UNLABELLED

Drug testing in patient biopsy-derived cells can identify potent treatments for patients suffering from relapsed or refractory hematologic cancers. Here we investigate the use of weakly supervised deep learning on cell morphologies (DML) to complement diagnostic marker-based identification of malignant and nonmalignant cells in drug testing. Across 390 biopsies from 289 patients with diverse blood cancers, DML-based drug responses show improved reproducibility and clustering of drugs with the same mode of action. DML does so by adapting to batch effects and by autonomously recognizing disease-associated cell morphologies. In a post hoc analysis of 66 patients, DML-recommended treatments led to improved progression-free survival compared with marker-based recommendations and physician's choice-based treatments. Treatments recommended by both immunofluorescence and DML doubled the fraction of patients achieving exceptional clinical responses. Thus, DML-enhanced ex vivo drug screening is a promising tool in the identification of effective personalized treatments.

SIGNIFICANCE

We have recently demonstrated that image-based drug screening in patient samples identifies effective treatment options for patients with advanced blood cancers. Here we show that using deep learning to identify malignant and nonmalignant cells by morphology improves such screens. The presented workflow is robust, automatable, and compatible with clinical routine. This article is highlighted in the In This Issue feature, p. 476.

摘要

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在患者活检衍生细胞中进行药物检测可以鉴定出复发或难治性血液系统癌症患者的有效治疗方法。在这里,我们研究了在药物检测中使用基于弱监督深度学习的细胞形态学(DML)来补充基于诊断标志物的恶性和非恶性细胞鉴定。在 289 名患有各种血液癌症的 390 名患者的活检样本中,基于 DML 的药物反应显示出改善的重现性和具有相同作用模式的药物聚类。DML 通过适应批次效应并自主识别与疾病相关的细胞形态来实现这一点。在对 66 名患者的事后分析中,与基于标志物的建议和医生选择的治疗相比,DML 推荐的治疗方法导致无进展生存期的改善。免疫荧光和 DML 推荐的治疗方法使达到卓越临床反应的患者比例增加了一倍。因此,基于 DML 的增强型体外药物筛选是鉴定有效个性化治疗方法的有前途的工具。

意义

我们最近证明,基于图像的患者样本药物筛选可鉴定出晚期血液癌患者的有效治疗选择。在这里,我们表明通过形态学使用深度学习来鉴定恶性和非恶性细胞可改善此类筛选。所提出的工作流程具有稳健性、可自动化并且与临床常规兼容。本文在本期的特色文章中进行了重点介绍,第 476 页。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/454a/9894727/1000a40d8594/502fig1.jpg

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