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昆明医科大学第一附属医院医学影像科,云南 650032
付凡欣(ROCID: 0009-0002-1258-2274),硕士研究生。
李 俊(ROCID: 0000-0002-6029-6451),硕士,副主任医师,E-mail: 6644814243@qq.com。
收稿:2025-04-14,
修回:2025-06-28,
纸质出版:2026-02-28
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付凡欣, 卢艳会, 王婉婷, 等. 基于Kaiser评分的乳腺癌多参数诊断预测模型的构建及效果评价[J]. 肿瘤影像学, 2026, 35(1): 72-83.
FU F X, LU Y H, WANG W TCitation:, et al. Construction and effectiveness evaluation of a multiparametric diagnosis prediction model for breast cancer based on Kaiser score[J]. Oncoradiology, 2026, 35(1): 72-83.
付凡欣, 卢艳会, 王婉婷, 等. 基于Kaiser评分的乳腺癌多参数诊断预测模型的构建及效果评价[J]. 肿瘤影像学, 2026, 35(1): 72-83. DOI: 10.19732/j.cnki.2096-6210.2026.01.010.
FU F X, LU Y H, WANG W TCitation:, et al. Construction and effectiveness evaluation of a multiparametric diagnosis prediction model for breast cancer based on Kaiser score[J]. Oncoradiology, 2026, 35(1): 72-83. DOI: 10.19732/j.cnki.2096-6210.2026.01.010.
目的
2
构建基于Kaiser评分的临床-影像多参数Kaiser诊断预测优化模型(简称“Kaiser
+
模型”)并进行验证,旨在提高对乳腺病灶恶性风险的诊断效能。
方法
2
收集2020年9月—2023年11月于昆明医科大学第一附属医院行乳腺X线摄影和磁共振成像(magnetic resonance imaging,MRI)检查的患者的临床及影像学资料,所有病灶均经病理学检查证实。将病灶按照7∶3的比例随机分成训练集和验证集。收集以下参数,临床因素包括患者年龄、初潮年龄、绝经情况、乳腺癌家族史、体重指数(body mass index,BMI);乳腺X线摄影影像参数包括纤维腺体类型、微钙化;乳腺MRI影像参数包括背景实质强化、病灶类型(肿块/非肿块)、形状、边缘、瘤周水肿、病灶内部强化模式、肿瘤周围血管征、时间-信号强度曲线(time-signal intensity curve,TIC)类型、弥散加权成像(diffusion-weighted imaging,DWI)边缘征、表观弥散系数(apparent diffusion coefficient,ADC)值、乳头凹陷、皮肤增厚或回缩。依据Kaiser评分流程图对每个病灶进行评分。采用
t
检验和
χ²
检验单因素分析筛选预测变量,采用多因素logistic回归构建诊断预测模型,绘制列线图。采用受试者工作特征(receiver operating characteristic,ROC)曲线的曲线下面积(area under curve,AUC)比较Kaiser
+
模型和Kaiser评分的诊断效能;绘制校准曲线评估模型的校准能力;采用决策曲线分析(decision curve analysis,DCA)评估模型在临床决策中的效用。
结果
2
本研究纳入347例患者,共347个病灶,其中恶性217个,良性130个。单因素分析显示,年龄、绝经情况、乳头凹陷、皮肤回缩/增厚、微钙化、病灶类型(肿块/非肿块)、形状、周围血管征、DWI边缘征、ADC是Kaiser评分所用指标之外的有效预测因素。Kaiser
+
模型及Kaiser评分在训练集中的AUC分别为0.962、0.914,差异有统计学意义(
Z
=3.363,
P
<
0.01),两者在验证集中的AUC分别为0.976、0.913,差异有统计学意义(
Z
=2.862,
P
<
0.01)。校准曲线显示Kaiser
+
模型的校准度良好;DCA显示Kaiser
+
模型具有较高的临床应用价值。
结论
2
本研究设计的Kaiser
+
模型能在术前用于预测乳腺病变性质,其诊断效能优于经典的Kaiser评分。
Objective
2
To construct and validate a clinical-imaging multiparametric Kaiser diagnostic prediction optimization model based on the Kaiser score (referred to as the Kaiser
+
model) for improving the efficacy of diagnosis of malignant risk in breast lesions.
Methods
2
Clinical and imaging data of patients who underwent mammography and breast magnetic resonance imaging (MRI) at the First Affiliated Hospital of Kunming Medical University from September 2020 to November 2023 were collected
and all lesions were confirmed pa
thologically. The lesions were randomly divided into a training set and a validation set in the ratio of 7∶3. The following parameters were collected
clinical factors: patient's age
age at menarche
menopausal status
family history of breast cancer status
body mass index (BMI); Mammography parameters: the amount of fibroglandular tissue (FGT)
microcalcification; Breast MRI parameters: background parenchymal enhancement (BPE)
lesion type (mass or non-mass)
shape
margins
peritumoral edema
internal enhancement pattern
adjacent vessel sign (AVS)
time-signal intensity curve (TIC)
diffusion-weighted imaging (DWI) rim sign
apparent diffusion coefficient (ADC) value
nipple invasion
skin thickening or retraction. Each lesion was scored according to the Kaiser score flow chart. The
t
test and
χ
2
test were used for univariate analysis to screen predictive variables
and multivariate logistic regression was used to construct the prediction model and draw the nomogram. Area under the receiver operating characteristic curve (AUC) were used to compare the diagnostic efficacy of Kaiser
+
model and Kaiser score. Calibration curves were plotted to assess the calibration of the model. Decision curve analysis (DCA) was used to evaluate the clinical validity of the model.
Results
2
A total of 347 patients were included in this study
with 347 lesions in total
among which 217 were malignant and 130 were benign. Univariate analysis showed that age
menopausal status
nipple invasion
skin thickening or retraction
microcalcification
lesion type (mass or non-mass)
shape
AVS
DWI edge sign
and ADC value were effective predictors other than those used in Kaiser score. In the training set
the AUCs of Kaiser
+
model and Kaiser score were 0.962 and 0.914
with statistically significant differences (
Z
=3.363
P
<
0.01). In the validation set
the AUCs of Kaiser
+
model and Kaiser score
were 0.976 and 0.913
with statistically significant differences (
Z
=2.862
P
<
0.01). The calibration curve showed that the Kaiser
+
model was well calibrated. DCA indicated that the Kaiser
+
model had high clinical application value.
Conclusion
2
The Kaiser
+
model designed in this study can be used to predict and diagnose the nature of breast lesions before operation
and its diagnostic performance is better than the classical Kaiser score.
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