Sandberg Dan, Tolmachev Vladimir, Velikyan Irina, Olofsson Helena, Wennborg Anders, Feldwisch Joachim, Carlsson Jörgen, Lindman Henrik, Sörensen Jens
Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Section of Nuclear Medicine and PET, Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.
Eur J Nucl Med Mol Imaging. 2017 Aug;44(8):1337-1346. doi: 10.1007/s00259-017-3650-3. Epub 2017 Mar 6.
PURPOSE: In phase I/II-studies radiolabelled ABY-025 Affibody molecules identified human epidermal growth factor receptor 2 (HER2) expression in breast cancer metastases using PET and SPECT imaging. Here, we wanted to investigate the utility of a simple intra-image normalization using tumour-to-reference tissue-ratio (T/R) as a HER2 status discrimination strategy to overcome potential issues related to cross-calibration of scanning devices. METHODS: Twenty-three women with pre-diagnosed HER2-positive/negative metastasized breast cancer were scanned with [In]-ABY-025 SPECT/CT (n = 7) or [Ga]-ABY-025 PET/CT (n = 16). Uptake was measured in all metastases and in normal spleen, lung, liver, muscle, and blood pool. Normal tissue uptake variation and T/R-ratios were established for various time points and for two different doses of injected peptide from a total of 94 whole-body image acquisitions. Immunohistochemistry (IHC) was used to verify HER2 expression in 28 biopsied metastases. T/R-ratios were compared to IHC findings to establish the best reference tissue for each modality and each imaging time-point. The impact of shed HER2 in serum was investigated. RESULTS: Spleen was the best reference tissue across modalities, followed by blood pool and lung. Spleen-T/R was highly correlated to PET SUV in metastases after 2 h (r = 0.96, P < 0.001) and reached an accuracy of 100% for discriminating IHC HER2-positive and negative metastases at 4 h (PET) and 24 h (SPECT) after injection. In a single case, shed HER2 resulted in intense tracer retention in blood. In the remaining patients shed HER2 was elevated, but without significant impact on ABY-025 biodistribution. CONCLUSION: T/R-ratios using spleen as reference tissue accurately quantify HER2 expression with radiolabelled ABY-025 imaging in breast cancer metastases with SPECT and PET. Tracer binding to shed HER2 in serum might affect quantification in the extreme case.
目的:在I/II期研究中,放射性标记的ABY - 025亲和体分子通过PET和SPECT成像确定了乳腺癌转移灶中人表皮生长因子受体2(HER2)的表达。在此,我们想研究使用肿瘤与参考组织比值(T/R)进行简单的图像内归一化作为HER2状态判别策略的实用性,以克服与扫描设备交叉校准相关的潜在问题。 方法:对23例预先诊断为HER2阳性/阴性转移性乳腺癌的女性进行了[铟]-ABY - 025 SPECT/CT(n = 7)或[镓]-ABY - 025 PET/CT(n = 16)扫描。在所有转移灶以及正常脾脏、肺、肝脏、肌肉和血池中测量摄取情况。从总共94次全身图像采集数据中,针对不同时间点以及两种不同剂量的注射肽,确定正常组织摄取变化和T/R比值。采用免疫组织化学(IHC)方法在28个活检转移灶中验证HER2表达。将T/R比值与IHC结果进行比较,以确定每种成像方式和每个成像时间点的最佳参考组织。研究了血清中脱落的HER2的影响。 结果:脾脏是所有成像方式中最佳的参考组织,其次是血池和肺。脾脏T/R与转移灶中PET的标准化摄取值(SUV)在注射后2小时高度相关(r = 0.96,P < 0.001),并且在注射后4小时(PET)和24小时(SPECT)时,区分IHC HER2阳性和阴性转移灶的准确率达到100%。在1例患者中,脱落的HER2导致示踪剂在血液中大量滞留。在其余患者中,脱落的HER2升高,但对ABY - 025的生物分布没有显著影响。 结论:以脾脏作为参考组织的T/R比值通过SPECT和PET的放射性标记ABY - 025成像准确量化了乳腺癌转移灶中的HER2表达。在极端情况下,示踪剂与血清中脱落的HER2结合可能会影响定量分析。
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