通过深度学习探索结直肠癌患者病理图像中的预后生物标记。

IF 3.4 2区 医学 Q1 PATHOLOGY
Binshen Wei, Linqing Li, Yenan Feng, Sihan Liu, Peng Fu, Lin Tian
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引用次数: 0

摘要

血色素和伊红(H&E)全切片图像为预测结直肠癌(CRC)患者的预后结果提供了宝贵的信息。然而,由于表型信息的微妙复杂性,从病理图像中提取预后指标具有挑战性。我们在前列腺癌、肺癌、结直肠癌和卵巢癌(PLCO)筛查试验数据集中 640 名结直肠癌患者的数据上训练了一个弱监督深度学习模型,并使用癌症基因组图谱(TCGA)数据集中 522 名结直肠癌患者的数据对其进行了验证。我们创建了结直肠癌风险评分(CRCRS)来评估患者的预后,使用 Grad-CAM 将风险评分的病理表型可视化,并利用 TCGA CRC 队列中的多组学数据来研究风险评分的潜在生物机制。总生存分析表明,CRCRS是PLCO队列的独立预后指标(p
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Exploring prognostic biomarkers in pathological images of colorectal cancer patients via deep learning

Exploring prognostic biomarkers in pathological images of colorectal cancer patients via deep learning

Hematoxylin and eosin (H&E) whole slide images provide valuable information for predicting prognostic outcomes in colorectal cancer (CRC) patients. However, extracting prognostic indicators from pathological images is challenging due to the subtle complexities of phenotypic information. We trained a weakly supervised deep learning model on data from 640 CRC patients in the prostate, lung, colorectal, and ovarian (PLCO) cancer screening trial dataset and validated it using data from 522 CRC patients in the cancer genome atlas (TCGA) dataset. We created the colorectal cancer risk score (CRCRS) to assess patient prognosis, visualized the pathological phenotype of the risk score using Grad-CAM, and employed multiomics data from the TCGA CRC cohort to investigate the potential biological mechanisms underlying the risk score. The overall survival analysis revealed that the CRCRS served as an independent prognostic indicator for both the PLCO cohort (p < 0.001) and the TCGA cohort (p < 0.001), with its predictive efficacy remaining unaffected by the clinical staging system. Additionally, satisfactory chemotherapeutic benefits were observed in stage II/III CRC patients with high CRCRS but not in those with low CRCRS. A pathomics nomogram constructed by integrating the CRCRS with the tumor-node-metastasis (TNM) staging system enhanced prognostic prediction accuracy compared with using the TNM staging system alone. Noteworthy features of the risk score were identified, such as immature tumor mesenchyme, disorganized gland structures, small clusters of cancer cells associated with unfavorable prognosis, and infiltrating inflammatory cells associated with favorable prognosis. The TCGA multiomics data revealed potential correlations between the CRCRS and the activation of energy production and metabolic pathways, the tumor immune microenvironment, and genetic mutations in APC, SMAD2, EEF1AKMT4, EPG5, and TANC1. In summary, our deep learning algorithm identified the CRCRS as a prognostic indicator in CRC, providing a significant approach for prognostic risk stratification and tailoring precise treatment strategies for individual patients.

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来源期刊
Journal of Pathology Clinical Research
Journal of Pathology Clinical Research Medicine-Pathology and Forensic Medicine
CiteScore
7.40
自引率
2.40%
发文量
47
审稿时长
20 weeks
期刊介绍: The Journal of Pathology: Clinical Research and The Journal of Pathology serve as translational bridges between basic biomedical science and clinical medicine with particular emphasis on, but not restricted to, tissue based studies. The focus of The Journal of Pathology: Clinical Research is the publication of studies that illuminate the clinical relevance of research in the broad area of the study of disease. Appropriately powered and validated studies with novel diagnostic, prognostic and predictive significance, and biomarker discover and validation, will be welcomed. Studies with a predominantly mechanistic basis will be more appropriate for the companion Journal of Pathology.
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