TY - JOUR T1 - Phase I Trial of the Positron-Emitting Arg-Gly-Asp (RGD) Peptide Radioligand <sup>18</sup>F-AH111585 in Breast Cancer Patients JF - Journal of Nuclear Medicine JO - J Nucl Med SP - 879 LP - 886 DO - 10.2967/jnumed.107.049452 VL - 49 IS - 6 AU - Laura M. Kenny AU - R. Charles Coombes AU - Inger Oulie AU - Kaiyumars B. Contractor AU - Matthew Miller AU - Terence J. Spinks AU - Brian McParland AU - Pamela S. Cohen AU - Ai-Min Hui AU - Carlo Palmieri AU - Safiye Osman AU - Matthias Glaser AU - David Turton AU - Adil Al-Nahhas AU - Eric O. Aboagye Y1 - 2008/06/01 UR - http://jnm.snmjournals.org/content/49/6/879.abstract N2 - The integrin αvβ3 receptor is upregulated on tumor cells and endothelium and plays important roles in angiogenesis and metastasis. Arg-Gly-Asp (RGD) peptide ligands have high affinity for these integrins and can be radiolabeled for PET imaging of angiogenesis or tumor development. We have assessed the safety, stability, and tumor distribution kinetics of a novel radiolabeled RGD-based integrin peptide-polymer conjugate, 18F-AH111585, and its feasibility to detect tumors in metastatic breast cancer patients using PET. Methods: The biodistribution of 18F-AH111585 was assessed in 18 tumor lesions from 7 patients with metastatic breast cancer by PET, and the PET data were compared with CT results. The metabolic stability of 18F-AH111585 was assessed by chromatography of plasma samples. Regions of interest (ROIs) defined over tumor and normal tissues of the PET images were used to determine the kinetics of radioligand binding in tissues. Results: The radiopharmaceutical and PET procedures were well tolerated in all patients. All 18 tumors detected by CT were visible on the 18F-AH111585 PET images, either as distinct increases in uptake compared with the surrounding normal tissue or, in the case of liver metastases, as regions of deficit uptake because of the high background activity in normal liver tissue. 18F-AH111585 was either homogeneously distributed in the tumors or appeared within the tumor rim, consistent with the pattern of viable peripheral tumor and central necrosis often seen in association with angiogenesis. Increased uptake compared with background (P = 0.002) was demonstrated in metastases in lung, pleura, bone, lymph node, and primary tumor. Conclusion: 18F-AH111585 designed to bind the αvβ3 integrin is safe, metabolically stable, and retained in tumor tissues and detects breast cancer lesions by PET in most anatomic sites. ER -