Sörensen Jens, Velikyan Irina, Sandberg Dan, Wennborg Anders, Feldwisch Joachim, Tolmachev Vladimir, Orlova Anna, Sandström Mattias, Lubberink Mark, Olofsson Helena, Carlsson Jörgen, Lindman Henrik
1. Section of Nuclear Medicine and PET, Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.
2. Affibody AB, Solna, Sweden.
Theranostics. 2016 Jan 1;6(2):262-71. doi: 10.7150/thno.13502. eCollection 2016.
Positron Emission Tomography (PET) imaging of HER2 expression could potentially be used to select patients for HER2-targed therapy, predict response based on uptake and be used for monitoring. In this phase I/II study the HER2-binding Affibody molecule ABY-025 was labeled with (68)Ga-gallium ([(68)Ga]ABY-025) for PET to study effect of peptide mass, test-retest variability and correlation of quantified uptake in tumors to histopathology.
Sixteen women with known metastatic breast cancer and on-going treatment were included and underwent FDG PET/CT to identify viable metastases. After iv injection of 212±46 MBq [(68)Ga]ABY-025 whole-body PET was performed at 1, 2 and 4 h. In the first 10 patients (6 with HER2-positive and 4 with HER2-negative primary tumors), [(68)Ga]ABY-025 PET/CT with two different doses of injected peptide was performed one week apart. In the last six patients (5 HER2-positive and 1 HER2-negative primary tumors), repeated [(68)Ga]ABY-025 PET were performed one week apart as a test-retest of uptake in individual lesions. Biopsies from 16 metastases in 12 patients were collected for verification of HER2 expression by immunohistochemistry and in-situ hybridization.
Imaging 4h after injection with high peptide content discriminated HER2-positive metastases best (p<0.01). PET SUV correlated with biopsy HER2-scores (r=0.91, p<0.001). Uptake was five times higher in HER2-positive than in HER2-negative lesions with no overlap (p=0.005). The test-retest intra-class correlation was r=0.996. [(68)Ga]ABY-025 PET correctly identified conversion and mixed expression of HER2 and targeted treatment was changed in 3 of the 16 patients.
[(68)Ga]ABY-025 PET accurately quantifies whole-body HER2-receptor status in metastatic breast cancer.
对HER2表达进行正电子发射断层扫描(PET)成像可能有助于选择接受HER2靶向治疗的患者,根据摄取情况预测疗效并用于监测。在这项I/II期研究中,将HER2结合亲合体分子ABY-025用(68)Ga-镓标记([(68)Ga]ABY-025)用于PET,以研究肽质量的影响、重测变异性以及肿瘤中定量摄取与组织病理学的相关性。
纳入16名已知转移性乳腺癌且正在接受治疗的女性,进行氟代脱氧葡萄糖(FDG)PET/CT以识别存活的转移灶。静脉注射212±46 MBq的[(68)Ga]ABY-025后,在1、2和4小时进行全身PET检查。在最初的10名患者(6名HER2阳性原发性肿瘤患者和4名HER2阴性原发性肿瘤患者)中,相隔一周进行两次不同剂量注射肽的[(68)Ga]ABY-025 PET/CT检查。在最后6名患者(5名HER2阳性原发性肿瘤患者和1名HER2阴性原发性肿瘤患者)中,相隔一周重复进行[(68)Ga]ABY-025 PET检查,作为对单个病灶摄取情况的重测。收集12名患者16个转移灶的活检样本,通过免疫组织化学和原位杂交验证HER2表达。
注射高肽含量后4小时成像对HER2阳性转移灶的鉴别效果最佳(p<0.01)。PET标准化摄取值(SUV)与活检HER2评分相关(r=0.91,p<0.001)。HER2阳性病灶的摄取量比HER2阴性病灶高5倍,且无重叠(p=0.005)。重测组内相关性为r=0.996。[(68)Ga]ABY-025 PET正确识别了16名患者中3名患者HER2的转化和混合表达,并改变了靶向治疗方案。
[(68)Ga]ABY-025 PET可准确量化转移性乳腺癌患者全身HER2受体状态。