Shen Yiyuan, Zhang Xu, Zheng Jinlong, Wang Simin, Ding Jie, Sun Shiyun, Bai Qianming, Fu Caixia, Wang Junlong, Gong Jing, You Chao, Gu Yajia
Department of Radiology, Fudan University Shanghai Cancer Center, 270 Dongan Road, Shanghai 200032, China.
Department of Oncology, Shanghai Medical College, Fudan University, 270 Dongan Road, Shanghai 200032, China.
Tomography. 2025 Mar 10;11(3):31. doi: 10.3390/tomography11030031.
The discovery of novel antibody-drug conjugates for low-expression human epidermal growth factor receptor 2 (HER2-low) breast cancer highlights the inadequacy of the conventional binary classification of HER2 status as either negative or positive. Identification of HER2-low breast cancer is crucial for selecting patients who may benefit from targeted therapies. This study aims to determine whether qualitative and quantitative magnetic resonance imaging (MRI) features can effectively reflect low-HER2-expression breast cancer.
Pre-treatment breast MRI images from 232 patients with pathologically confirmed breast cancer were retrospectively analyzed. Both clinicopathologic and MRI features were recorded. Qualitative MRI features included Breast Imaging Reporting and Data System (BI-RADS) descriptors from dynamic contrast-enhanced MRI (DCE-MRI), as well as intratumoral T2 hyperintensity and peritumoral edema observed in T2-weighted imaging (T2WI). Quantitative features were derived from diffusion kurtosis imaging (DKI) using multiple b-values and included statistics such as mean, median, 5th and 95th percentiles, skewness, kurtosis, and entropy from apparent diffusion coefficient (ADC), D, and K histograms. Differences in clinicopathologic, qualitative, and quantitative MRI features were compared across groups, with multivariable logistic regression used to identify significant independent predictors of HER2-low breast cancer. The discriminative power of MRI features was assessed using receiver operating characteristic (ROC) curves.
HER2 status was categorized as HER2-zero (n = 60), HER2-low (n = 91), and HER2-overexpressed (n = 81). Clinically, estrogen receptor (ER), progesterone receptor (PR), hormone receptor (HR), and Ki-67 levels significantly differed between the HER2-low group and others (all < 0.001). In MRI analyses, intratumoral T2 hyperintensity was more prevalent in HER2-low cases ( = 0.009, = 0.008). Mass lesions were more common in the HER2-zero group than in the HER2-low group ( = 0.038), and mass shape ( < 0.001) and margin ( < 0.001) significantly varied between the HER2 groups, with mass shape emerging as an independent predictive factor (HER2-low vs. HER2-zero: = 0.010, HER2-low vs. HER2-over: = 0.012). Qualitative MRI features demonstrated an area under the curve (AUC) of 0.763 (95% confidence interval [CI]: 0.667-0.859) for distinguishing HER2-low from HER2-zero status. Quantitative features showed distinct differences between HER2-low and HER2-overexpression groups, particularly in non-mass enhancement (NME) lesions. Combined variables achieved the highest predictive accuracy for HER2-low status, with an AUC of 0.802 (95% CI: 0.701-0.903).
Qualitative and quantitative MRI features offer valuable insights into low-HER2-expression breast cancer. While qualitative features are more effective for mass lesions, quantitative features are more suitable for NME lesions. These findings provide a more accessible and cost-effective approach to noninvasively identifying patients who may benefit from targeted therapy.
新型抗体药物偶联物用于低表达人表皮生长因子受体2(HER2低表达)乳腺癌的发现凸显了将HER2状态传统二分法分类为阴性或阳性的不足。识别HER2低表达乳腺癌对于选择可能从靶向治疗中获益的患者至关重要。本研究旨在确定定性和定量磁共振成像(MRI)特征是否能有效反映低HER2表达乳腺癌。
回顾性分析232例经病理证实的乳腺癌患者的治疗前乳腺MRI图像。记录临床病理特征和MRI特征。定性MRI特征包括动态对比增强MRI(DCE-MRI)的乳腺影像报告和数据系统(BI-RADS)描述符,以及在T2加权成像(T2WI)中观察到的瘤内T2高信号和瘤周水肿。定量特征来自使用多个b值的扩散峰度成像(DKI),包括表观扩散系数(ADC)、扩散系数(D)和峰度系数(K)直方图的均值、中位数、第5和第95百分位数、偏度、峰度和熵等统计量。比较各组间临床病理、定性和定量MRI特征的差异,采用多变量逻辑回归确定HER2低表达乳腺癌的显著独立预测因子。使用受试者操作特征(ROC)曲线评估MRI特征的鉴别能力。
HER2状态分为HER2零表达(n = 60)、HER2低表达(n = 91)和HER2过表达(n = 81)。临床上,HER2低表达组与其他组之间的雌激素受体(ER)、孕激素受体(PR)、激素受体(HR)和Ki-67水平存在显著差异(均P < 0.001)。在MRI分析中,瘤内T2高信号在HER2低表达病例中更常见(P = 0.009,P = 0.008)。HER2零表达组的肿块病变比HER2低表达组更常见(P = 0.038),HER2组之间的肿块形状(P < 0.001)和边缘(P < 0.001)有显著差异,肿块形状成为独立预测因子(HER2低表达与HER2零表达:P = 0.010,HER2低表达与HER2过表达:P = 0.012)。定性MRI特征在区分HER2低表达与HER2零表达状态时曲线下面积(AUC)为0.763(95%置信区间[CI]:0.667 - 0.859)。定量特征在HER2低表达和HER2过表达组之间显示出明显差异,特别是在非肿块强化(NME)病变中。联合变量对HER2低表达状态的预测准确性最高。AUC为0.802(95%CI:0.701 - 0.903)。
定性和定量MRI特征为低HER2表达乳腺癌提供了有价值的见解。虽然定性特征对肿块病变更有效,但定量特征更适合NME病变。这些发现为非侵入性识别可能从靶向治疗中获益的患者提供了一种更易获得且具有成本效益的方法。