Journal
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING
Volume 41, Issue 11, Pages 2008-2016Publisher
SPRINGER
DOI: 10.1007/s00259-014-2839-y
Keywords
Quantitative metabolic parameters-metabolic tumour volume Outcome; Oesophageal carcinoma; Chemoradiotherapy; PET/CT
Funding
- Ligue Contre le Cancer de Haute Normandie
- North West Canceropole (National Cancer Institute - INCa)
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Purpose It has been suggested that FDG PET has predictive value for the prognosis of treated oesophageal carcinoma. However, the studies reported in the literature have shown discordant results. The aim of this study was to determine whether pretherapy quantitative metabolic parameters correlate with patient outcomes. Methods Included in the study were 67 patients with a histological diagnosis of oesophageal squamous cell carcinoma. Each patient underwent F-18-FDG PET (4.5 MBq/kg) before chemoradiotherapy. Quantitative analysis was performed using the following parameters: age, weight loss, location, N stage, OMS performance status, MTVp and MTVp' (metabolic tumour volume determined by two different physicians), MTV40% (volume for a threshold of 40% of SUVmax), MTVa (volume automatically determined with a contrast-based adaptive threshold method), SUVmax, SUVmean and TLG (total lesion glycolysis). Results MTVp and MTV40% were highly correlated (Pearson's index 0.92). SUVmean(p) and SUVmean(40%) were also correlated (Pearson's index 0.86), as were TLG(p) and TLG(40%) (Pearson's index 0.98). Similarly, the parameters obtained with the adaptive threshold method (MTVa, SUVmean(a) and TLG(a)) were correlated with those obtained manually (MTVp, SUVmean(p) and TLG(p)). The manual metabolic tumour volume determination (MTVp and MTVp') was reproducible. Multivariate analysis for disease-free survival (DFS) showed that a larger MTVp was associated with a shorter DFS (p=0.004) and that a higher SUVmax was associated with a longer DFS (p=0.02). Multivariate analysis for overall survival (OS) showed that a larger MTVp was associated with a shorter OS (p=0.01) and that a tumour in the distal oesophagus was associated with a longer OS (p=0.005). The associations among the other parameters were not statistically significant. Conclusion Metabolic tumour volume is a major prognostic factor for DFS and OS in patients with oesophageal squamous cell carcinoma. Higher SUVmax values were paradoxically associated with longer survival. The location of the tumour also appeared to affect prognosis.
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