TY - JOUR
T1 - PET of HER2-positive pulmonary metastases with 18F-Z HER2:342 affibody in a murine model of breast cancer
T2 - Comparison with 18F-FDG
AU - Kramer-Marek, Gabriela
AU - Bernardo, Marcelino
AU - Kiesewetter, Dale O.
AU - Bagci, Ulas
AU - Kuban, Monika
AU - Omer, Aras
AU - Zielinski, Rafal
AU - Seidel, Jurgen
AU - Choyke, Peter
AU - Capala, Jacek
PY - 2012/6
Y1 - 2012/6
N2 - Targeted therapies often depend on the expression of the target present in the tumor. This expression can be difficult to ascertain in widespread metastases. 18F-FDG PET/CT, although sensitive, is nonspecific for particular tumor markers. Here, we compare the use of a human epidermal growth factor receptor 2 (HER2)-specific 18F-Z HER2:342-Affibody and 18F-FDG in HER2-expressing pulmonary metastases in a murine model of breast cancer. Methods: The lung metastasis model was established by intravenous injection of MDA-MB-231 HER2-Luc human breast cancer cells into the tail vein. Bioluminescence imaging was used to evaluate metastasis progression. Uptake of 18F-Z HER2:342-Affibody and 18F-FDG was confirmed by coregistration of the PET images with MR and CT images. At the end of the study, the presence of neoplastic cells and HER2 expression in lung tissues, and distribution of the tracer, were assessed ex vivo by immunohistochemistry and autoradiography. Results: 18F-Z HER2:342-Affibody successfully targeted HER2-positive lesions in the lung and allowed detection of metastases as early as 9 wk after injection of cells. In contrast, 18F-FDG uptake was often masked by surrounding inflammatory changes and was nonspecific for HER2 expression. HER2 expression at a cellular level correlated well with tracer uptake on autoradiography. Conclusion: 18F-Z HER2:342-Affibody is a promising tracer for evaluation of HER2 status of breast cancer metastases and is more specific for detecting HER2-positive lesions than 18F-FDG.
AB - Targeted therapies often depend on the expression of the target present in the tumor. This expression can be difficult to ascertain in widespread metastases. 18F-FDG PET/CT, although sensitive, is nonspecific for particular tumor markers. Here, we compare the use of a human epidermal growth factor receptor 2 (HER2)-specific 18F-Z HER2:342-Affibody and 18F-FDG in HER2-expressing pulmonary metastases in a murine model of breast cancer. Methods: The lung metastasis model was established by intravenous injection of MDA-MB-231 HER2-Luc human breast cancer cells into the tail vein. Bioluminescence imaging was used to evaluate metastasis progression. Uptake of 18F-Z HER2:342-Affibody and 18F-FDG was confirmed by coregistration of the PET images with MR and CT images. At the end of the study, the presence of neoplastic cells and HER2 expression in lung tissues, and distribution of the tracer, were assessed ex vivo by immunohistochemistry and autoradiography. Results: 18F-Z HER2:342-Affibody successfully targeted HER2-positive lesions in the lung and allowed detection of metastases as early as 9 wk after injection of cells. In contrast, 18F-FDG uptake was often masked by surrounding inflammatory changes and was nonspecific for HER2 expression. HER2 expression at a cellular level correlated well with tracer uptake on autoradiography. Conclusion: 18F-Z HER2:342-Affibody is a promising tracer for evaluation of HER2 status of breast cancer metastases and is more specific for detecting HER2-positive lesions than 18F-FDG.
KW - Affibody molecules
KW - F-FDG
KW - HER2
KW - PET imaging
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U2 - 10.2967/jnumed.111.100354
DO - 10.2967/jnumed.111.100354
M3 - Article
C2 - 22582046
AN - SCOPUS:84861851113
SN - 0161-5505
VL - 53
SP - 939
EP - 946
JO - Journal of Nuclear Medicine
JF - Journal of Nuclear Medicine
IS - 6
ER -