4.4 Article

[18F]FDG-PET/CT and long-term responses to everolimus in advanced neuroendocrine neoplasia

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JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
卷 44, 期 4, 页码 811-818

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SPRINGER
DOI: 10.1007/s40618-020-01378-3

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Neuroendocrine neoplasia; Everolimus; F-18-fluorodeoxyglucose PET; CT; Ki67; Tumor progression; Long-term response

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This study aimed to investigate the correlation between FDG-PET findings and responses to everolimus therapy in patients with neuroendocrine neoplasia, and identify predictors of long-term efficacy. The results showed that everolimus is a valid therapeutic option for well-differentiated NEN, even in patients with positive FDG-PET findings.
Purpose This study aims to identify in patients with neuroendocrine neoplasia (NEN) the potential correlation between FDG-PET findings and responses to everolimus therapy to identify predictors of long-term efficacy. Methods Retrospective analysis of patients with sporadic, advanced, progressive NEN treated with everolimus was performed based on the available data on FDG-PET patients obtained before commencing therapy. Data are expressed as the median (25-75th IQR). Risk factor analysis and survival analysis were performed by logistic regression and Cox proportional hazard regression and the determination of Kaplan-Meier curves, as appropriate. Results Sixty-six patients were evaluated (NET G1 19.7%, NET G2 75.7%, and NET G3 4.6%), including 45.4% with positive FDG-PET findings. Overall, disease stabilization and a partial response were achieved for 71.2% and 6% of patients, respectively. A long-term response (> 24 months) was observed in 33% of patients. Ki67 was the only predictor of tumor progression (p = 0.03). No significant difference in clinical outcomes was observed between patients with positive or negative FDG-PET findings (median PFS was 24 months and 18 months, respectively,p = 0.337; the disease control rate was 83.3% and 70%, respectively,p = 0.245). Conclusions Everolimus is a valid therapeutic option for advanced, progressive, well-differentiated NEN, even in patients with positive FDG-PET findings.

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