Usefulness of 18F-α-Methyltyrosine PET for Therapeutic Monitoring of Patients with Advanced Lung Cancer

L-[3- F]-α-methyl tyrosine ( F-FAMT) positron emission tomography (PET) has a high specificity for detecting malignant lesions. However, the usefulness of therapeutic monitoring of F-FAMT PET against advanced human neoplasms remains unclear. Here, we evaluated F-FAMT PET clinical significance regard...

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Published inAnticancer research Vol. 36; no. 12; pp. 6481 - 6490
Main Authors Kaira, Kyoichi, Higuchi, Tetsuya, Sunaga, Noriaki, Arisaka, Yukiko, Hisada, Takeshi, Tominaga, Hideyuki, Oriuchi, Noboru, Asao, Takayuki, Tsushima, Yoshihito, Yamada, Masanobu
Format Journal Article
LanguageEnglish
Published Greece 01.12.2016
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Summary:L-[3- F]-α-methyl tyrosine ( F-FAMT) positron emission tomography (PET) has a high specificity for detecting malignant lesions. However, the usefulness of therapeutic monitoring of F-FAMT PET against advanced human neoplasms remains unclear. Here, we evaluated F-FAMT PET clinical significance regarding therapy response and outcome after systemic chemotherapy in patients with advanced lung cancer, compared to F-FDG PET. All patients with untreated advanced lung cancer received F-FAMT PET and F-FDG PET before and 4 weeks after one cycle of chemotherapy. Metabolic response (MR) was defined according to the PERCIST guideline. Ninety-five patients were eligible for analysis on both PET scans. The histological type included 87 non-small cell lung cancers and 8 small-cell lung cancers. Post-treatment maximal standardized uptake values (SUV ) and MR on F-FAMT PET were correlated with tumor response. In all patients, post-treatment SUV of F-FDG and F-FAMT PET and MR of F-FAMT PET were statistically significant prognostic markers for predicting poor outcome by univariate analysis. Multivariate analysis confirmed that MR on F-FAMT PET was a significant independent prognostic factor. MR on F-FAMT PET may be a potential parameter to predict the prognosis after first-line chemotherapy in patients with advanced lung cancer.
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ISSN:0250-7005
1791-7530
DOI:10.21873/anticanres.11247