4.7 Article

Total 18F-FDG PET/CT Metabolic Tumor Volume Is Associated With Postoperative Biochemical Response in Patients With Metastatic Pheochromocytomas and Paragangliomas

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ANNALS OF SURGERY
卷 263, 期 3, 页码 582-587

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/SLA.0000000000001018

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18F-FDG PET; CT; metabolic tumor volume; metastatic pheochromocytoma; paraganglioma; total lesion glycolysis

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  1. Center for Cancer Research, National Cancer Institute, National Institutes of Health

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Objective:The aim of this pilot study was to determine if metabolic tumor volume (MTV) and total lesion glycolysis (TLG) could serve as predictors of biochemical remission and pharmacotherapy-free interval in patients with metastatic pheochromocytomas (PCCs) and paragangliomas (PGLs).Background:Patients with metastatic PCCs/PGLs have a high rate of biochemical recurrence, which can be associated with increased cardiovascular morbidity. Predictors of biochemical response are needed to guide and select patients who may benefit from therapy.Methods:Whole body MTV and TLG was calculated from preoperative 18F-FDG PET/CT scans and analyzed as marker of biochemical response and pharmacotherapy-free interval.Results:Seventeen patients underwent a total of 19 procedures, with a median follow-up time of 26.4 months. Whole body MTV of patients with biochemical recurrence (n=13, mean 73.8mL) was higher than those who had a biochemical response (n=6, mean 14.7mL, P=0.05). Patients with low MTV (<37.2mL) had an improved durable partial biochemical response (P<0.05), and a statistical trend for complete biochemical remission (P=0.07) and pharmacotherapy-free interval (P=0.06). In 8 patients with metastatic disease outside the abdomen, 4 patients had less than 35% of their disease burden outside the abdomen and these patients had a more durable partial biochemical response compared to patients with greater than 35% of their disease burden outside the abdomen (P<0.05).Conclusions:Whole body MTV and TLG represents novel and valuable predictors of biochemical response for patients with metastatic PCCs and PGLs. A larger prospective study should be performed to validate these findings.

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