Prognostic role of metabolic parameters of 18F-FDG PET-CT scan performed during radiation therapy in locally advanced head and neck squamous cell carcinoma

Purpose To evaluate the prognostic value of 18 F-FDG PET-CT performed in the third week (iPET) of definitive radiation therapy (RT) in patients with newly diagnosed locally advanced mucosal primary head and neck squamous-cell-carcinoma (MPHNSCC). Methodology Seventy-two patients with MPHNSCC treated...

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Published inEuropean journal of nuclear medicine and molecular imaging Vol. 42; no. 13; pp. 1984 - 1994
Main Authors Min, Myo, Lin, Peter, Lee, Mark T., Shon, Ivan Ho, Lin, Michael, Forstner, Dion, Bray, Victoria, Chicco, Andrew, Tieu, Minh Thi, Fowler, Allan
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer Berlin Heidelberg 2015
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Summary:Purpose To evaluate the prognostic value of 18 F-FDG PET-CT performed in the third week (iPET) of definitive radiation therapy (RT) in patients with newly diagnosed locally advanced mucosal primary head and neck squamous-cell-carcinoma (MPHNSCC). Methodology Seventy-two patients with MPHNSCC treated with radical RT underwent staging PET-CT and iPET. The maximum standardised uptake value (SUV max ), metabolic tumour volume (MTV) and total lesional glycolysis (TLG) of primary tumour (PT) and index node (IN) [defined as lymph node(s) with highest TLG] were analysed, and results were correlated with loco-regional recurrence-free survival (LRFS), disease-free survival (DFS), metastatic failure-free survival(MFFS) and overall survival (OS), using Kaplan-Meier analysis. Results Optimal cutoffs (OC) were derived from receiver operating characteristic curves: SUV max-PT  = 4.25 g/mL, MTV PT  = 3.3 cm 3 , TLG PT  = 9.4 g, for PT, and SUV max-IN  = 4.05 g/mL, MTV IN  = 1.85 cm 3 and TLG IN  = 7.95 g for IN. Low metabolic values in iPET for PT below OC were associated with statistically significant better LRFS and DFS. TLG was the best predictor of outcome with 2-year LRFS of 92.7 % vs. 71.1 % [ p  = 0.005, compared with SUV max ( p  = 0.03) and MTV ( p  = 0.022)], DFS of 85.9 % vs. 60.8 % [ p  = 0.005, compared with SUV max ( p  = 0.025) and MTV ( p  = 0.018)], MFFS of 85.9 % vs. 83.7 % [ p  = 0.488, compared with SUV max ( p  = 0.52) and MTV ( p  = 0.436)], and OS of 81.1 % vs. 75.0 % [ p  = 0.279, compared with SUV max ( p  = 0.345) and MTV ( p  = 0.512)]. There were no significant associations between the percentage reduction of primary tumour metabolic parameters and outcomes. In patients with nodal disease, metabolic parameters below OC (for both PT and IN) were significantly associated with all oncological outcomes, while TLG was again the best predictor: LRFS of 84.0 % vs. 55.3 % ( p  = 0.017), DFS of 79.4 % vs. 38.6 % ( p  = 0.001), MFFS 86.4 % vs. 68.2 % ( p  = 0.034) and OS 80.4 % vs. 55.7 % ( p  = 0.045). Conclusion The metabolic parameters of iPET can be useful predictors of patient outcome and potentially have a role in adaptive therapy for MPHNSCC. Among the three parameters, TLG was found to be the best prognostic indicator of oncological outcomes.
ISSN:1619-7070
1619-7089
DOI:10.1007/s00259-015-3104-8