From the Department of Radiology (T.R., E.L., C.N., L.R., L.I., M.D., C.M., A.T.), Department of Diagnostic and Theranostic Medicine-Pathology (L.D.), and Department of Medical Oncology (L.C.), Institut Curie Paris, PSL Research University, 26 rue d'Ulm, Paris, France; Department of Radiology (G.J.) and Department of Diagnostic and Theranostic Medicine-Pathology (E.M.), Institut Curie St Cloud, PSL Research University, St Cloud, France.
Radiology. 2023 Aug;308(2):e222646. doi: 10.1148/radiol.222646.
Background Half of breast cancers exhibit low expression levels of human epidermal growth factor receptor 2 (HER2) and can be targeted by new antibody-drug conjugates. The imaging differences between HER2-zero (immunohistochemistry [IHC] score of 0), HER2-low (IHC score of 1+ or 2+ with negative findings at fluorescence in situ hybridization [FISH]), and HER2-positive (IHC score of 2+ with positive findings at FISH or IHC score of 3+) breast cancers were unknown. Purpose To assess whether multiparametric dynamic contrast-enhanced MRI-based radiomic features can help distinguish HER2 expressions in breast cancer. Materials and Methods This study included women with breast cancer who underwent MRI at two different centers between December 2020 and December 2022. Tumor segmentation and radiomic feature extraction were performed on T2-weighted and dynamic contrast-enhanced T1-weighted images. Unsupervised correlation analysis of reproducible features and least absolute shrinkage and selector operation were used for the selection of features to build a radiomics signature. The area under the receiver operating characteristic curve (AUC) was used to assess the performance of the radiomic signature. Multivariable logistic regression was used to identify independent predictors for distinguishing HER2 expressions in both the training and prospectively acquired external data set. Results The training set included 208 patients from center 1 (mean age, 53 years ± 14 [SD]), and the external test set included 131 patients from center 2 (mean age, 54 years ± 13). In the external test data set, the radiomic signature achieved an AUC of 0.80 (95% CI: 0.71, 0.89) for distinguishing HER2-low and -positive tumors versus HER2-zero tumors and was a significant predictive factor for distinguishing these two groups (odds ratio = 7.6; 95% CI: 2.9, 19.8; < .001). Among HER2-low or -positive breast cancers, histology type, associated nonmass enhancement, and multiple lesions at MRI had an AUC of 0.77 (95% CI: 0.68, 0.86) in the external test set for the prediction of HER2-positive versus HER2-low cancers. Conclusion The radiomic signature and tumor descriptors from multiparametric breast MRI may predict distinct HER2 expressions of breast cancers with therapeutic implications. © RSNA, 2023 See also the editorial by Kataoka and Honda in this issue.
背景 半数乳腺癌患者的人表皮生长因子受体 2(HER2)表达水平较低,可通过新型抗体药物偶联物进行靶向治疗。HER2-0(免疫组化 [IHC] 评分 0)、HER2-低(IHC 评分 1+或 2+,荧光原位杂交 [FISH] 阴性)和 HER2-阳性(FISH 阳性或 IHC 评分 3+)乳腺癌之间的影像学差异尚不清楚。目的 评估多参数动态对比增强 MRI 基于放射组学特征是否有助于区分乳腺癌的 HER2 表达。 材料与方法 本研究纳入了 2020 年 12 月至 2022 年 12 月在两个不同中心接受 MRI 检查的乳腺癌女性患者。在 T2 加权和动态对比增强 T1 加权图像上进行肿瘤分割和放射组学特征提取。使用重复特征的无监督相关性分析和最小绝对收缩和选择操作(least absolute shrinkage and selector operation,LASSO)选择特征,以构建放射组学特征。受试者工作特征曲线下面积(area under the receiver operating characteristic curve,AUC)用于评估放射组学特征的性能。多变量逻辑回归用于确定区分训练集和前瞻性外部数据集 HER2 表达的独立预测因素。 结果 训练集包括来自中心 1 的 208 名患者(平均年龄,53 岁±14[标准差]),外部测试集包括来自中心 2 的 131 名患者(平均年龄,54 岁±13)。在外部测试数据集,放射组学特征区分 HER2-低和阳性肿瘤与 HER2-0 肿瘤的 AUC 为 0.80(95%置信区间:0.71,0.89),是区分这两组的显著预测因素(比值比=7.6;95%置信区间:2.9,19.8;<0.001)。在 HER2-低或阳性乳腺癌中,组织学类型、伴发非肿块样强化和 MRI 上的多发病灶在外部测试集预测 HER2-阳性与 HER2-低癌症的 AUC 为 0.77(95%置信区间:0.68,0.86)。 结论 多参数乳腺 MRI 的放射组学特征和肿瘤描述符可能有助于预测具有治疗意义的不同 HER2 表达的乳腺癌。