Mansur Ameer, McConathy Jonathan E, Stringer-Reasor Erica, Rocque Gabrielle, Khoury Katia, Eltoum Noon, Nikpanah Moozhan, Bartels Jennifer, Wright Brian, Jahan Nusrat, Jeffers Denise, Lapi Suzanne E, Sorace Anna G
Department of Biomedical Engineering, University of Alabama at Birmingham, Birmingham, Alabama.
O'Neal Comprehensive Cancer Center, University of Alabama, Birmingham, Alabama.
J Nucl Med. 2025 Jul 1;66(7):1018-1026. doi: 10.2967/jnumed.124.268931.
Current methods for evaluating HER2 expression in breast cancer are invasive and fail to capture spatial and temporal heterogeneity between primary tumors and metastases. Nuclear imaging allows for whole-body, noninvasive assessment of human epidermal growth factor receptor 2 (HER2) and can distinguish between HER2-positive and HER2-negative lesions. MRI offers superior soft-tissue contrast and quantitative metrics, such as the apparent diffusion coefficient (ADC) from diffusion-weighted (DW) imaging, providing prognostic value. The goal of this study was to present quantitative imaging metrics from [Zr]Zr-trastuzumab PET and simultaneous DW-MRI to characterize HER2-positive metastatic breast cancer lesions. The secondary aim was to explore the utility of combining [Zr]Zr-trastuzumab PET with DW-MRI for intratumoral habitat mapping using multiparametric [Zr]Zr-trastuzumab PET/MRI to enhance characterization of lesions and assess the response to HER2-targeted therapy. Fifteen patients with confirmed HER2-positive breast cancer underwent simultaneous PET/MRI 5-7 d after receiving 77 ± 1.9 MBq of [Zr]Zr-trastuzumab. Whole-body ADC maps were generated from DW-MRI, and regions of interest in normal and malignant tissues were delineated. Imaging metrics included SUV for PET and ADC for DW-MRI. Threshold- and clustering-based methods were applied for intratumoral characterization through multiparametric mapping. Malignant tissues exhibited significantly higher [Zr]Zr-trastuzumab uptake than did normal tissues. High uptake in the kidneys, liver, and blood pool complicated lesion identification near these tissues. ADC mapping improved lesion characterization in the brain, soft tissue, and bone. The diagnostic accuracy of [Zr]Zr-trastuzumab PET alone improved when combined with ADC mapping (area under the curve, 0.59 and 0.75, respectively). Multiparametric analysis revealed intratumoral heterogeneity, identifying distinct subregions with variable tracer uptake and diffusion characteristics. Combining [Zr]Zr-trastuzumab PET with DW-MRI offers a multiparametric imaging approach for characterizing HER2 expression and cellular density in HER2-positive metastatic breast cancer. Increased tracer uptake in malignant lesions and improved lesion characterization through ADC mapping highlight the potential of this combination for evaluating treatment response and tumor heterogeneity. Large-scale validation is needed to confirm these findings and support integrating [Zr]Zr-trastuzumab PET and DW-MRI into clinical management for better patient outcomes.
目前评估乳腺癌中HER2表达的方法具有侵入性,且无法捕捉原发性肿瘤与转移灶之间的空间和时间异质性。核成像可对人表皮生长因子受体2(HER2)进行全身无创评估,并能区分HER2阳性和HER2阴性病变。MRI具有出色的软组织对比度和定量指标,如扩散加权(DW)成像中的表观扩散系数(ADC),具有预后价值。本研究的目的是展示来自[Zr]Zr-曲妥珠单抗PET和同步DW-MRI的定量成像指标,以表征HER2阳性转移性乳腺癌病变。次要目的是探索将[Zr]Zr-曲妥珠单抗PET与DW-MRI相结合用于瘤内栖息地映射的效用,使用多参数[Zr]Zr-曲妥珠单抗PET/MRI来增强病变表征并评估对HER2靶向治疗的反应。15例确诊为HER2阳性乳腺癌的患者在接受77±1.9 MBq的[Zr]Zr-曲妥珠单抗后5 - 7天接受同步PET/MRI检查。从DW-MRI生成全身ADC图,并勾勒出正常和恶性组织中的感兴趣区域。成像指标包括PET的SUV和DW-MRI的ADC。通过多参数映射应用基于阈值和聚类的方法进行瘤内表征。恶性组织显示出比正常组织显著更高的[Zr]Zr-曲妥珠单抗摄取。肾脏、肝脏和血池中的高摄取使这些组织附近的病变识别变得复杂。ADC映射改善了脑、软组织和骨中的病变表征。[Zr]Zr-曲妥珠单抗PET单独使用时与ADC映射相结合,诊断准确性得到提高(曲线下面积分别为0.59和0.75)。多参数分析揭示了瘤内异质性,识别出具有不同示踪剂摄取和扩散特征的不同亚区域。将[Zr]Zr-曲妥珠单抗PET与DW-MRI相结合提供了一种多参数成像方法,用于表征HER2阳性转移性乳腺癌中的HER2表达和细胞密度。恶性病变中示踪剂摄取增加以及通过ADC映射改善病变表征突出了这种组合在评估治疗反应和肿瘤异质性方面的潜力。需要大规模验证来证实这些发现,并支持将[Zr]Zr-曲妥珠单抗PET和DW-MRI纳入临床管理以实现更好的患者预后。