Xie T, Huang A L, Xiang L Y, Xue H C, Chen Z Z, Ma A L, Yan H L, Yuan J P
Department of Pathology, Renmin Hospital of Wuhan University, Wuhan430060, China.
Zhonghua Bing Li Xue Za Zhi. 2025 Jan 8;54(1):59-65. doi: 10.3760/cma.j.cn112151-20240712-00455.
To investigate the prognostic value of deep learning-based automated quantification of tumor-stroma ratio (TSR) in patients undergoing neoadjuvant therapy (NAT) for breast cancer. Specimens were collected from 209 breast cancer patients who received NAT at Renmin Hospital of Wuhan University from October 2019 to June 2023. TSR levels in pre-NAT biopsy specimens were automatically computed using a deep learning algorithm and categorized into low stroma (TSR≤30%), intermediate stroma (TSR 30% to ≤60%), and high stroma (TSR>60%) groups. Residual cancer burden (RCB) grading of post-NAT surgical specimens was determined to compare the relationship between TSR expression levels and RCB grades. The correlation of TSR with NAT efficacy was analyzed, and the association between TSR expression and patient prognosis was further investigated. There were 85 cases with low stroma (TSR≤30%), 93 cases with intermediate stroma (TSR 30% to ≤60%), and 31 cases with high stroma (TSR>60%). Different TSR expression levels showed significant differences between various RCB grades (<0.05). Logistic univariate and multivariate analyses showed that TSR was a risk factor for obtaining a complete pathological remission from neoadjuvant therapy for breast cancer when it was used as a continuous variable (<0.05); COX regression and survival analyses showed that the lower the percentage of tumorigenic mesenchyme was, the better the prognosis of the patient was (<0.05). The deep learning-based model enables automatic and accurate quantification of TSR. A lower pre-treatment tumoral stroma is associated with a lower RCB score and a higher rate of pathologic complete response, indicating that TSR can predict the efficacy of neoadjuvant therapy in breast cancer and thus holds prognostic significance. Therefore, TSR may serve as a biomarker for predicting therapeutic outcomes in breast cancer neoadjuvant therapy.
为研究基于深度学习的肿瘤-基质比(TSR)自动定量分析在接受乳腺癌新辅助治疗(NAT)患者中的预后价值。收集了2019年10月至2023年6月在武汉大学人民医院接受NAT的209例乳腺癌患者的标本。使用深度学习算法自动计算NAT前活检标本中的TSR水平,并将其分为低基质(TSR≤30%)、中基质(TSR 30%至≤60%)和高基质(TSR>60%)组。确定NAT后手术标本的残余癌负担(RCB)分级,以比较TSR表达水平与RCB分级之间的关系。分析TSR与NAT疗效的相关性,并进一步研究TSR表达与患者预后的关联。低基质(TSR≤30%)组85例,中基质(TSR 30%至≤60%)组93例,高基质(TSR>60%)组31例。不同TSR表达水平在各RCB分级之间存在显著差异(<0.05)。Logistic单因素和多因素分析显示,当TSR作为连续变量时,它是乳腺癌新辅助治疗获得完全病理缓解的危险因素(<0.05);COX回归和生存分析显示,致瘤间充质百分比越低,患者预后越好(<0.05)。基于深度学习的模型能够自动、准确地定量TSR。治疗前肿瘤基质较低与较低的RCB评分和较高的病理完全缓解率相关,表明TSR可预测乳腺癌新辅助治疗的疗效,因此具有预后意义。因此,TSR可能作为预测乳腺癌新辅助治疗疗效的生物标志物。