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一种利用冰冻切片分析预测保乳手术中切缘阳性的术中列线图。

An intraoperative nomogram for predicting secondary margin positivity in breast conserving surgery utilizing frozen section analysis.

作者信息

Li Cheng, Jiang Yan, Wu Xumiao, Luo Yong, Li Qi

机构信息

Department of Breast and Thyroid Surgery, Ningbo Medical Center Lihuili Hospital, Ningbo, Zhejiang, China.

Department of Ultrasound, Ningbo Medical Center Lihuili Hospital, Ningbo, Zhejiang, China.

出版信息

Front Oncol. 2025 Jan 7;14:1366467. doi: 10.3389/fonc.2024.1366467. eCollection 2024.

DOI:10.3389/fonc.2024.1366467
PMID:39839802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11746899/
Abstract

BACKGROUND

Breast conserving surgery (BCS) is a standard treatment for breast cancer. Intraoperative frozen section analysis (FSA) is widely used for margin assessment in BCS. In addition, FSA-assisted excisional biopsy is still commonly practiced in many developing countries. The aim of this study is to develop a predictive model applicable to BCS with FSA-assisted excisional biopsy and margin assessment, with a focus on predicting the risk of secondary margin positivity in re-excision procedures following positive initial margins. This may reduce surgical complications and healthcare costs associated with multiple re-excisions and FSAs for recurrent positive margins.

METHODS

Patients were selected, divided into training and testing sets, and their data were collected. The Least Absolute Shrinkage and Selection Operator (LASSO) was used to identify significant variables from the training set for model building. Model performance was evaluated using Receiver Operating Characteristic (ROC) curves, calibration curves, and Decision Curve Analyses (DCAs). An optimal threshold identified by the Youden index was validated using sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV).

RESULTS

The study included 348 patients (256 in the training set, 92 in the testing set). No significant statistical differences were found between the sets. LASSO identified six variables to construct the model and corresponding nomogram. The model showed good discrimination (mean area under the curve (AUC) values of 0.79 in the training set and 0.83 in the testing set), calibration (Hosmer-Lemeshow test results (-values 0.214 in the training set, 0.167 in testing set)) and clinical utility. The optimal threshold was set at 97 points in the nomogram, yielding a sensitivity of 0.66 (0.54-0.77), specificity of 0.80 (0.74-0.85), PPV of 0.56 (0.47-0.64) and NPV of 0.86 (0.82-0. 90) for the training set, and a sensitivity of 0.65 (0.46-0.84), specificity of 0.88 (0.79-0.95), PPV of 0.68 (0.53-0.85) and NPV of 0.87 (0.81-0.93) for the testing set, demonstrating the model's effectiveness in both sets.

CONCLUSIONS

This study successfully developed a novel predictive model for secondary margin positivity applicable to BCS with FSA-assisted excisional biopsy and margin assessment. It demonstrates good discriminative ability, calibration, and clinical utility.

摘要

背景

保乳手术(BCS)是乳腺癌的标准治疗方法。术中冰冻切片分析(FSA)广泛用于保乳手术中的切缘评估。此外,FSA辅助切除活检在许多发展中国家仍普遍应用。本研究的目的是开发一种适用于FSA辅助切除活检和切缘评估的保乳手术预测模型,重点是预测初次切缘阳性后再次切除手术中二次切缘阳性的风险。这可能会减少与多次再次切除和因复发性阳性切缘进行的FSA相关的手术并发症和医疗费用。

方法

选择患者,分为训练集和测试集,并收集其数据。使用最小绝对收缩和选择算子(LASSO)从训练集中识别用于模型构建的显著变量。使用受试者工作特征(ROC)曲线、校准曲线和决策曲线分析(DCA)评估模型性能。使用约登指数确定的最佳阈值通过灵敏度、特异度、阳性预测值(PPV)和阴性预测值(NPV)进行验证。

结果

该研究纳入了348例患者(训练集256例,测试集92例)。两组之间未发现显著统计学差异。LASSO识别出六个变量来构建模型和相应的列线图。该模型显示出良好的区分度(训练集曲线下面积(AUC)平均值为0.79,测试集为0.83)、校准度(Hosmer-Lemeshow检验结果,训练集P值为0.214,测试集为0.167)和临床实用性。列线图中的最佳阈值设定为97分,训练集的灵敏度为0.66(0.54 - 0.77),特异度为0.80(0.74 - 0.85),PPV为0.56(0.47 - 0.64),NPV为0.86(0.82 - 0.90);测试集的灵敏度为0.65(0.46 - 0.84),特异度为0.88(0.79 - 0.95),PPV为0.68(0.53 - 0.85),NPV为0.87(0.81 - 0.93),证明了该模型在两组中的有效性。

结论

本研究成功开发了一种适用于FSA辅助切除活检和切缘评估的保乳手术二次切缘阳性的新型预测模型。它显示出良好的区分能力、校准度和临床实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dbe/11746899/1db2a3cf57de/fonc-14-1366467-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dbe/11746899/3305a655c48f/fonc-14-1366467-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dbe/11746899/bc6fddc62359/fonc-14-1366467-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dbe/11746899/444cce9e042d/fonc-14-1366467-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dbe/11746899/6ef649b5e7f5/fonc-14-1366467-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dbe/11746899/e6db4c885513/fonc-14-1366467-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dbe/11746899/1db2a3cf57de/fonc-14-1366467-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dbe/11746899/3305a655c48f/fonc-14-1366467-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dbe/11746899/bc6fddc62359/fonc-14-1366467-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dbe/11746899/444cce9e042d/fonc-14-1366467-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dbe/11746899/6ef649b5e7f5/fonc-14-1366467-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dbe/11746899/e6db4c885513/fonc-14-1366467-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dbe/11746899/1db2a3cf57de/fonc-14-1366467-g006.jpg

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