Department of Otolaryngology, Head and Neck Surgery, University Hospital Zurich, Frauenklinikstrasse 24, 8091, Zurich, Switzerland.
Eur Arch Otorhinolaryngol. 2010 Oct;267(10):1635-40. doi: 10.1007/s00405-010-1348-2. Epub 2010 Aug 3.
(18)F-fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET)/CT imaging of squamous cell carcinoma of the head and neck (HNSCC) renders the possibility to study metabolic tumor activity by measuring FDG-uptake expressed as maximum standardized uptake value (SUV(max)). A correlation between SUV(max) and several factors including T-classification, histological tumor differentiation or different anatomic subsites is of potential interest in HNSCC. The aim of this study was to evaluate how metabolic tumor activity derived from FDG-PET correlates with prognostic clinical and pathological parameters including these factors. 262 patients with HNSCC undergoing PET/CT for initial staging were assessed separately for a potential correlation between SUV(max) and T-classification, histological grading, and anatomical subsites of the primary tumor. Nonparametric testing showed a significant correlation between SUV(max) and T-classification (P < 0.001). On the contrary, no statistically significant correlation was found between SUV(max) and histological tumor grading. Furthermore, no statistical significant correlation between the different anatomical subsites and SUV(max) were found. There was no significant correlation of SUV(max) and tumor grading after adjustment for T-stage and anatomical localization of the tumor, neither.
Metabolic tumor activity correlates with T-stage of HNSCC. However, histological tumor grading does not correlate with SUV(max). The role of primary tumor SUV(max) as a predictor of outcome or survival remains unclear. Clinicians should therefore exercise caution in attributing any clinical importance to SUV(max) obtained from a single PET/CT exam.
评估头颈部鳞状细胞癌(HNSCC)中来源于 FDG-PET 的代谢肿瘤活性与包括这些因素在内的预后临床和病理参数之间的相关性。
对 262 例接受初始分期 PET/CT 的 HNSCC 患者分别评估 SUV(max)与 T 分类、组织学分级和原发肿瘤解剖部位之间的潜在相关性。非参数检验显示 SUV(max)与 T 分类之间存在显著相关性(P<0.001)。相反,SUV(max)与组织学肿瘤分级之间无统计学显著相关性。此外,不同解剖部位与 SUV(max)之间也无统计学显著相关性。对 T 分期和肿瘤解剖定位进行调整后,SUV(max)与肿瘤分级之间也没有显著相关性。
代谢肿瘤活性与 HNSCC 的 T 分期相关。然而,组织学肿瘤分级与 SUV(max)不相关。原发肿瘤 SUV(max)作为预后或生存的预测因子的作用仍不清楚。因此,临床医生在从单次 PET/CT 检查中获得的 SUV(max)中赋予任何临床重要性时应谨慎。