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组织病理学图像的深度学习分析可预测非小细胞肺癌的免疫治疗预后并揭示肿瘤微环境特征

英文原题:Deep learning analysis of histopathological images predicts immunotherapy prognosis and reveals tumour microenvironment features in non-small cell lung cancer.

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Deep learning analysis of histopathological images predicts immunotherapy prognosis and reveals tumour microenvironment features in non-small cell lung cancer.

PubMed 2024/10/25(内容时间) Br J Cancer Q1 · IF 7.8(JCR 2025)

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研究概要

基于深度学习的 ir-PPS 特征可从 H&E 图像中预测 NSCLC 患者的 ICIs 预后。ir-PPS 提供了一种新的影像学生物标志物,可能有助于在 NSCLC 中选择 ICIs 治疗的最佳候选者。

研究思路结论见上方概要

非小细胞肺癌(NSCLC)是全球癌症死亡的主要原因之一。免疫检查点抑制剂(ICIs)已成为晚期NSCLC患者的重要治疗选择。然而,只有一部分患者能从ICIs中获得临床获益。因此,识别能够预测ICIs反应的生物标志物对于优化患者选择至关重要。

NSCLC患者的苏木精-伊红(H&E)图像来自本地队列(n = 106)和癌症基因组图谱(TCGA)(n = 899)。我们基于H&E染色组织病理学图像开发了一种ICI相关病理预后特征(ir-PPS),利用深度学习预测接受ICIs治疗的NSCLC患者的预后。为实现这一目标,我们采用了改进的ResNet模型(ResNet18-PG),这是一种广泛使用的深度学习架构,以其在处理复杂图像识别任务方面的有效性而闻名。我们的改进包括采用渐进增长策略以提高模型训练的稳定性,以及使用AdamW优化器,该优化器通过根据训练动态调整学习率来增强优化过程。

深度学习模型ResNet18-PG在本地队列中实现了0.918的受试者工作特征曲线下面积(AUC)和0.995的召回率。ir-PPS有效对NSCLC患者进行了风险分层。低风险组(n = 40)患者在接受ICI治疗后的无进展生存期(PFS)显著优于高风险组(n = 66,log-rank P = 0.004,风险比(HR)= 3.65,95%CI:1.75-7.60)。ir-PPS在预测6个月PFS(AUC = 0.750)、12个月PFS(AUC = 0.677)和18个月PFS(AUC = 0.662)方面表现出良好的区分能力。低风险组表现出免疫检查点分子、细胞毒性相关基因表达增加,TIL(肿瘤浸润淋巴细胞)丰度升高,以及免疫刺激通路活性增强。

展开英文摘要原文

Non-small cell lung cancer (NSCLC) is one of the leading causes of cancer mortality worldwide. Immune checkpoint inhibitors (ICIs) have emerged as a crucial treatment option for patients with advanced NSCLC. However, only a subset of patients experience clinical benefit from ICIs. Therefore, identifying biomarkers that can predict response to ICIs is imperative for optimising patient selection.

Hematoxylin and eosin (H&E) images of NSCLC patients were obtained from the local cohort (n = 106) and The Cancer Genome Atlas (TCGA) (n = 899). We developed an ICI-related pathological prognostic signature (ir-PPS) based on H&E stained histopathology images to predict prognosis in NSCLC patients treated with ICIs using deep learning. To accomplish this, we employed a modified ResNet model (ResNet18-PG), a widely-used deep learning architecture well-known for its effectiveness in handling complex image recognition tasks. Our modifications include a progressive growing strategy to improve the stability of model training and the use of the AdamW optimiser, which enhances the optimisation process by adjusting the learning rate based on training dynamics.

The deep learning model, ResNet18-PG, achieved an area under the receiver operating characteristic curve (AUC) of 0.918 and a recall of 0.995 on the local cohort. The ir-PPS effectively risk-stratified NSCLC patients. Patients in the low-risk group (n = 40) had significantly improved progression-free survival (PFS) after ICI treatment compared to those in the high-risk group (n = 66, log-rank P = 0.004, hazard ratio (HR) = 3.65, 95%CI: 1.75-7.60). The ir-PPS demonstrated good discriminatory power for predicting 6-month PFS (AUC = 0.750), 12-month PFS (AUC = 0.677), and 18-month PFS (AUC = 0.662). The low-risk group exhibited increased expression of immune checkpoint molecules, cytotoxicity-related genes, an elevated abundance of tumour-infiltrating lymphocytes, and enhanced activity in immune stimulatory pathways.

The ir-PPS signature derived from H&E images using deep learning could predict ICIs prognosis in NSCLC patients. The ir-PPS provides a novel imaging biomarker that may help select optimal candidates for ICIs therapy in NSCLC.

论文信息

作者
Wang Y、Ju X、Hua R、Chen J、Dai X、Liu L、Wang G、Bai Y
第一作者单位
Department of Thoracic Surgery, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, China.China
通讯作者单位
Department of Respiratory and Critical Care Medicine, Sixth People's Hospital of Chengdu, Chengdu, Sichuan, China. 383152721@qq.com.China
期刊
British journal of cancer2024 Dec
原文标识
PubMed 39455880 · DOI 10.1038/s41416-024-02856-8