Prognostic significance of collagen signatures at breast tumor boundary obtained by combining multiphoton imaging and imaging analysis.

IF 4.9 2区 医学 Q2 CELL BIOLOGY Cellular Oncology Pub Date : 2024-02-01 Epub Date: 2023-08-22 DOI:10.1007/s13402-023-00851-4
Xingxin Huang, Fangmeng Fu, Wenhui Guo, Deyong Kang, Xiahui Han, Liqin Zheng, Zhenlin Zhan, Chuan Wang, Qingyuan Zhang, Shu Wang, Shunwu Xu, Jianli Ma, Lida Qiu, Jianxin Chen, Lianhuang Li
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Abstract

Purpose: Collagen features in breast tumor microenvironment is closely associated with the prognosis of patients. We aim to explore the prognostic significance of collagen features at breast tumor border by combining multiphoton imaging and imaging analysis.

Methods: We used multiphoton microscopy (MPM) to label-freely image human breast tumor samples and then constructed an automatic classification model based on deep learning to identify collagen signatures from multiphoton images. We recognized three kinds of collagen signatures at tumor boundary (CSTB I-III) in a small-scale, and furthermore obtained a CSTB score for each patient based on the combined CSTB I-III by using the ridge regression analysis. The prognostic performance of CSTB score is assessed by the area under the receiver operating characteristic curve (AUC), Cox proportional hazard regression analysis, as well as Kaplan-Meier survival analysis.

Results: As an independent prognostic factor, statistical results reveal that the prognostic performance of CSTB score is better than that of the clinical model combining three independent prognostic indicators, molecular subtype, tumor size, and lymph nodal metastasis (AUC, Training dataset: 0.773 vs. 0.749; External validation: 0.753 vs. 0.724; HR, Training dataset: 4.18 vs. 3.92; External validation: 4.98 vs. 4.16), and as an auxiliary indicator, it can greatly improve the accuracy of prognostic prediction. And furthermore, a nomogram combining the CSTB score with the clinical model is established for prognosis prediction and clinical decision making.

Conclusion: This standardized and automated imaging prognosticator may convince pathologists to adopt it as a prognostic factor, thereby customizing more effective treatment plans for patients.

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结合多光子成像和成像分析获得的乳腺肿瘤边界胶原特征的预后意义。
目的:乳腺肿瘤微环境中的胶原蛋白特征与患者的预后密切相关。我们旨在结合多光子成像和成像分析,探讨乳腺肿瘤边界胶原蛋白特征的预后意义:方法:我们使用多光子显微镜(MPM)对人类乳腺肿瘤样本进行无标记成像,然后构建了一个基于深度学习的自动分类模型,从多光子图像中识别胶原蛋白特征。我们在小范围内识别了肿瘤边界的三种胶原蛋白特征(CSTB I-III),并根据CSTB I-III的组合,通过脊回归分析得出了每位患者的CSTB评分。通过接收者操作特征曲线下面积(AUC)、Cox比例危险回归分析以及Kaplan-Meier生存分析评估CSTB评分的预后效果:统计结果显示,作为一个独立的预后因素,CSTB评分的预后效果优于结合分子亚型、肿瘤大小和淋巴结转移三个独立预后指标的临床模型(AUC,训练数据集:0.773 vs. 0.749; External validation:外部验证:0.753 vs. 0.724;HR,训练数据集:4.18 vs. 3.92):4.18 vs. 3.92; External validation:4.98 vs. 4.16),作为辅助指标,可以大大提高预后预测的准确性。此外,还建立了一个将CSTB评分与临床模型相结合的提名图,用于预后预测和临床决策:结论:这一标准化和自动化的影像预后指标可能会说服病理学家将其作为预后因素,从而为患者定制更有效的治疗方案。
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来源期刊
Cellular Oncology
Cellular Oncology ONCOLOGY-CELL BIOLOGY
CiteScore
10.30
自引率
1.50%
发文量
86
审稿时长
12 months
期刊介绍: The Official Journal of the International Society for Cellular Oncology Focuses on translational research Addresses the conversion of cell biology to clinical applications Cellular Oncology publishes scientific contributions from various biomedical and clinical disciplines involved in basic and translational cancer research on the cell and tissue level, technical and bioinformatics developments in this area, and clinical applications. This includes a variety of fields like genome technology, micro-arrays and other high-throughput techniques, genomic instability, SNP, DNA methylation, signaling pathways, DNA organization, (sub)microscopic imaging, proteomics, bioinformatics, functional effects of genomics, drug design and development, molecular diagnostics and targeted cancer therapies, genotype-phenotype interactions. A major goal is to translate the latest developments in these fields from the research laboratory into routine patient management. To this end Cellular Oncology forms a platform of scientific information exchange between molecular biologists and geneticists, technical developers, pathologists, (medical) oncologists and other clinicians involved in the management of cancer patients. In vitro studies are preferentially supported by validations in tumor tissue with clinicopathological associations.
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