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基于全切片图像的直肠癌无监督人工智能预后预测

Whole slide image based prognosis prediction in rectal cancer using unsupervised artificial intelligence.

作者信息

Zhou Xuezhi, Dai Jing, Lu Yizhan, Zhao Qingqing, Liu Yong, Wang Chang, Zhao Zongya, Wang Chong, Gao Zhixian, Yu Yi, Zhao Yandong, Cao Wuteng

机构信息

College of Medical Engineering, Xinxiang Medical University, No. 601, Jinsui Road, Xinxiang, Henan, 453003, China.

Engineering Technology Research Center of Neurosense and Control of Henan Province, Xinxiang, China.

出版信息

BMC Cancer. 2024 Dec 18;24(1):1523. doi: 10.1186/s12885-024-13292-5.

Abstract

BACKGROUND

Rectal cancer is a common cancer worldwide and lacks effective prognostic markers. The development of prognostic markers by computational pathology methods has attracted increasing attention. This paper aims to construct a prognostic signature from whole slide images for predicting progression-free survival (PFS) of rectal cancer through an unsupervised artificial intelligence algorithm.

METHODS

A total of 238 patients with rectal cancer from two datasets were collected for the development and validation of the prognostic signature. A tumor detection model was built by transfer learning. Then, on the basis of the tumor patches recognized by the tumor detection model, a convolutional autoencoder model was built for decoding the tumor patches into deep latent features. Next, on the basis of the deep latent features, the tumor patches were divided into different clusters. The cluster number and other hyperparameters were optimized by a nested cross-validation method. The percentage of each cluster from the patient's tumor patches, which is hereafter called PCF, was calculated for prognostic signature construction. The prognostic signature was constructed by Cox proportional hazard regression with L2 regularization. Finally, bioinformatic analysis was performed to explore the underlying biological mechanisms of the PCFs.

RESULTS

The accuracy of the tumor detection model in distinguishing tumor patches from non-tumor patches achieved 99.3%. The optimal cluster number was determined to be 9. Therfore, 9 PCFs were calculated to construct the prognostic signature. The prognostic signature achieved a concordance index of 0.701 in the validation cohort. The Kaplan-Meier survival curves showed the prognostic signature had good risk stratification ability. Through the bioinformatic analysis, several PCF-associated genes were identified. These genes were enriched in various gene ontology terms.

CONCLUSION

The developed prognostic signature can effectively predict PFS in patients with rectal cancer and exploration of the underlying biological mechanisms may help to promote its clinical translation.

摘要

背景

直肠癌是全球常见的癌症,缺乏有效的预后标志物。通过计算病理学方法开发预后标志物已引起越来越多的关注。本文旨在通过无监督人工智能算法从全切片图像构建预后特征,以预测直肠癌的无进展生存期(PFS)。

方法

收集来自两个数据集的238例直肠癌患者用于预后特征的开发和验证。通过迁移学习建立肿瘤检测模型。然后,基于肿瘤检测模型识别出的肿瘤切片,构建卷积自动编码器模型,将肿瘤切片解码为深度潜在特征。接下来,基于深度潜在特征,将肿瘤切片分为不同的簇。通过嵌套交叉验证方法优化簇数和其他超参数。计算患者肿瘤切片中每个簇的百分比(以下简称PCF)用于构建预后特征。通过带有L2正则化的Cox比例风险回归构建预后特征。最后,进行生物信息学分析以探索PCF的潜在生物学机制。

结果

肿瘤检测模型区分肿瘤切片和非肿瘤切片的准确率达到99.3%。确定最佳簇数为9。因此,计算9个PCF以构建预后特征。预后特征在验证队列中的一致性指数为0.701。Kaplan-Meier生存曲线显示预后特征具有良好的风险分层能力。通过生物信息学分析,鉴定了几个与PCF相关的基因。这些基因在各种基因本体术语中富集。

结论

所开发的预后特征可以有效预测直肠癌患者的PFS,对潜在生物学机制的探索可能有助于促进其临床转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c77/11658449/3bc7b7234367/12885_2024_13292_Fig1_HTML.jpg

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