RT Journal Article SR Electronic T1 Evaluation of LAT1 tracer 18F-FAMT in the inflammatory lesions -comparison study with 18F-FDG PET JF Journal of Nuclear Medicine JO J Nucl Med FD Society of Nuclear Medicine SP 1108 OP 1108 VO 59 IS supplement 1 A1 Sakai, Tatsuya A1 Watabe, Tadashi A1 Hirai, Nobuto A1 Tani, Naoki A1 Ikeda, Hayato A1 Naka, Sadahiro A1 Kanai, Yasukazu A1 Tatsumi, Mitsuaki A1 Shimosegawa, Eku A1 Hatazawa, Jun YR 2018 UL http://jnm.snmjournals.org/content/59/supplement_1/1108.abstract AB 1108Objectives: 18F-FDG is mainly used as an oncology PET-tracer. However, 18F-FDG can show false positive findings because it also accumulates in the inflammatory lesion. L-[3-18F]-α-methyl tyrosine (18F-FAMT) is reported as a tumor specific tracer as a substrate of L-type amino acid transporter 1 (LAT1), which is expressed in major cancer cells but not in normal tissue. The purpose of this study was to evaluate 18F-FAMT as a next oncology PET tracer by comparing with 18F-FDG. [Method] Four mice with inflammation (NOD mouse, body weight = 22.3 ± 0.3 g, 8 weeks old) were investigated in this study. Mouse model of inflammation was established by subcutaneous injection of turpentine oil (0.05 ml) in the bilateral flank regions. Static PET scans were performed 50min after the intravenous injection of 18F-FDG at day 4 (20.8 ± 2.4 MBq), and 18F-FAMT at day 5 (20.1 ± 1.2 MBq) under isoflurane anesthesia. Volumes of interest were placed on the inflammatory lesion to measure SUV using Pmod software (ver 3.6). Uptakes of the lesions were compared between 18F-FAMT and 18F-FDG by paired t-test. [Result] Visual analysis showed that uptakes of 18F-FAMT in the inflammatory lesions were almost as low as the background level. To the contrary, moderate uptakes were observed on 18F-FDG PET. The SUVmax of the inflammatory lesions were 1.37 ± 0.11 in the 18F-FDG PET and 0.37 ± 0.05 in the 18F-FAMT PET. The SUVmax of 18F-FAMT was significantly lower than that of 18F-FDG (p<0.01 by paired t-test). [Conclusion] 18F-FDG showed high uptakes on inflammatory lesions as previously reported. 18F-FAMT showed lower accumulation in inflammation compared to 18F-FDG and it is expected to be a tumor specific PET tracer to reduce false positive findings in the clinical oncology.