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利用深度学习从乳腺癌间质组织学预测新辅助化疗获益

英文原题:Predicting neoadjuvant chemotherapy benefit using deep learning from stromal histology in breast cancer.

查看英文原题

Predicting neoadjuvant chemotherapy benefit using deep learning from stromal histology in breast cancer.

PubMed 2022/11/22(内容时间) NPJ Breast Cancer Q1 · IF 8.4(JCR 2025)

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中文摘要

新辅助化疗(NAC)是局部晚期乳腺癌的标准治疗选择。然而,并非所有患者都能从NAC中获益;部分患者甚至在治疗后获得更差的结局。因此,治疗获益的预测因素对于指导临床决策至关重要。在此,我们通过基于深度学习(DL)的方法研究了乳腺癌间质组织学的预测潜力,并提出了肿瘤相关间质评分(TS-score),用于在多中心数据集中预测NAC的病理完全缓解(pCR)。TS-score被证明是pCR的独立预测因素,它不仅优于基线变量和间质TIL(肿瘤浸润淋巴细胞)(sTILs),还显著提高了基于基线变量模型的预测性能。此外,我们发现与淋巴细胞不同,间质中的胶原蛋白和成纤维细胞可能与NAC的不良反应相关。TS-score有潜力在NAC背景下更好地对乳腺癌患者进行分层。

展开英文摘要原文

Neoadjuvant chemotherapy (NAC) is a standard treatment option for locally advanced breast cancer.

However, not all patients benefit from NAC; some even obtain worse outcomes after therapy. Hence, predictors of treatment benefit are crucial for guiding clinical decision-making.

Here, we investigated the predictive potential of breast cancer stromal histology via a deep learning (DL)-based approach and proposed the tumor-associated stroma score (TS-score) for predicting pathological complete response (pCR) to NAC with a multicenter dataset. The TS-score was demonstrated to be an independent predictor of pCR, and it not only outperformed the baseline variables and stromal tumor-infiltrating lymphocytes (sTILs) but also significantly improved the prediction performance of the baseline variable-based model.

Furthermore, we discovered that unlike lymphocytes, collagen and fibroblasts in the stroma were likely associated with a poor response to NAC. The TS-score has the potential to better stratify breast cancer patients in NAC settings.

论文信息

作者
Li F、Yang Y、Wei Y、Zhao Y、Fu J、Xiao X、Zheng Z、Bu H
第一作者单位
Department of Pathology, West China Hospital, Sichuan University, Chengdu, China.China
通讯作者单位
Department of Pathology, West China Hospital, Sichuan University, Chengdu, China. hongbu@scu.edu.cn.China
期刊
NPJ breast cancer2022 Nov 22
原文标识
PubMed 36418332 · DOI 10.1038/s41523-022-00491-1