Detection of HER2 expression using (99m)Tc-NM-02 nanobody in patients with breast cancer: a non-randomized, non-blinded clinical trial

使用 (99m)Tc-NM-02 纳米抗体检测乳腺癌患者 HER2 表达:一项非随机、非盲临床试验

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Abstract

BACKGROUND: (99m)Tc radiolabeled nanobody NM-02 ((99m)Tc-NM-02) is a novel single photon emission computed tomography (SPECT) probe with a high affinity and specificity for human epidermal growth factor receptor 2 (HER2). In this study, a clinical imaging trial was conducted to investigate the relationship between (99m)Tc-NM-02 uptake and HER2 expression in patients with breast cancer. METHODS: Thirty patients with pathologically confirmed breast cancer were recruited and imaged with both (99m)Tc-NM-02 SPECT/computed tomography (CT) and (18)F-fluorodeoxyglucose ((18)F-FDG) positron emission tomography (PET)/CT. According to the treatment conditions before recruitment, patients were divided into two groups, the newly diagnosed group (n = 24) and the treated group (n = 6). The maximal standard uptake value (SUV(max)) of (18)F-FDG and SUV(max) and mean SUV (SUV(mean)) of (99m)Tc-NM-02 in the lesions were determined to analyze the relationship with HER2 expression. RESULTS: No meaningful relationship was observed between (18)F-FDG uptake and HER2 expression in 30 patients with breast cancer. (99m)Tc-NM-02 uptake was positively correlated with HER2 expression in the newly diagnosed group, but no correlation was observed in the treated group. (99m)Tc-NM-02 uptake in HER2-positive lesions was lower in those with effective HER2-targeted therapy compared with the newly diagnosed group. (99m)Tc-NM-02 SPECT/CT detected brain and bone metastases of breast cancer with a different imaging pattern from (18)F-FDG PET/CT. (99m)Tc-NM-02 showed no non-specific uptake in inflamed tissues and revealed intra- and intertumoral HER2 heterogeneity by SPECT/CT imaging in 9 of the 30 patients with breast cancer. CONCLUSIONS: (99m)Tc-NM-02 SPECT/CT has the potential for visualizing whole-body HER2 overexpression in untreated patients, making it a promising method for HER2 assessment in patients with breast cancer. TRIAL REGISTRATION: NCT04674722, Date of registration: December 19, 2020.

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