CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:A real-world clinicopathological model for predicting pathological complete response to neoadjuvant chemotherapy in breast cancer.
A real-world clinicopathological model for predicting pathological complete response to neoadjuvant chemotherapy in breast cancer.
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所开发的预测模型在预测接受 NAC 治疗的乳腺癌患者 pCR 方面展现出稳健的性能,标志着向乳腺癌更个性化治疗策略迈出了一步。
本研究旨在开发并验证一个临床病理模型,用于预测乳腺癌患者对新辅助化疗(NAC)的病理完全缓解(pCR),并确定关键预后因素。
本回顾性研究分析了2011年至2021年在浙江省人民医院接受NAC的279例乳腺癌患者的数据。此外,还使用了外部验证数据集进行模型验证,该数据集包含2022年至2023年来自兰溪市人民医院和浙江大学医学院附属第二医院的50例患者。建立了一个多因素logistic回归模型,纳入基线和NAC后的临床、超声特征、循环肿瘤细胞(CTCs)和病理变量。评估了模型预测pCR的性能。通过生存分析确定了预后因素。
在入组的279例患者中,pCR率达到27.96%(279例中78例)。该预测模型纳入了间质TIL(肿瘤浸润淋巴细胞)(sTIL)水平、Ki-67表达、分子亚型及超声回声特征等独立预测因子。该模型对pCR表现出较强的预测准确性(C-statistics/AUC 0.874),尤其是在HER2富集型(C-statistics/AUC 0.878)和三阴性(C-statistics/AUC 0.870)亚型中,且该模型在外部验证数据集中表现良好(C-statistics/AUC 0.836)。在CTC检测亚组中,纳入NAC后循环肿瘤细胞(CTC)变化及肿瘤大小变化进一步提高了预测性能(C-statistics/AUC 0.945)。关键预后因素包括肿瘤大小>5cm、淋巴结转移、sTIL水平、ER状态及pCR。尽管pCR率存在差异,但各分子亚型在接受标准全身治疗后的总体预后一致。
This study aimed to develop and validate a clinicopathological model to predict pathological complete response (pCR) to neoadjuvant chemotherapy (NAC) in breast cancer patients and identify key prognostic factors.
This retrospective study analyzed data from 279 breast cancer patients who received NAC at Zhejiang Provincial People's Hospital from 2011 to 2021. Additionally, an external validation dataset, comprising 50 patients from Lanxi People's Hospital and Second Affiliated Hospital, Zhejiang University School of Medicine from 2022 to 2023 was utilized for model verification. A multivariate logistic regression model was established incorporating clinical, ultrasound features, circulating tumor cells (CTCs), and pathology variables at baseline and post-NAC. Model performance for predicting pCR was evaluated. Prognostic factors were identified using survival analysis.
In the 279 patients enrolled, a pathologic complete response (pCR) rate of 27.96% (78 out of 279) was achieved. The predictive model incorporated independent predictors such as stromal tumor-infiltrating lymphocyte (sTIL) levels, Ki-67 expression, molecular subtype, and ultrasound echo features. The model demonstrated strong predictive accuracy for pCR (C-statistics/AUC 0.874), especially in human epidermal growth factor receptor 2 (HER2)-enriched (C-statistics/AUC 0.878) and triple-negative (C-statistics/AUC 0.870) subtypes, and the model performed well in external validation data set (C-statistics/AUC 0.836). Incorporating circulating tumor cell (CTC) changes post-NAC and tumor size changes further improved predictive performance (C-statistics/AUC 0.945) in the CTC detection subgroup. Key prognostic factors included tumor size >5cm, lymph node metastasis, sTIL levels, estrogen receptor (ER) status and pCR. Despite varied pCR rates, overall prognosis after standard systemic therapy was consistent across molecular subtypes.
The developed predictive model showcases robust performance in forecasting pCR in NAC-treated breast cancer patients, marking a step toward more personalized therapeutic strategies in breast cancer.
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