Department of Radiology, Boston Medical Center and Boston University School of Medicine, Boston, MA 02118, USA.
AJR Am J Roentgenol. 2011 Oct;197(4):976-80. doi: 10.2214/AJR.10.4884.
The purpose of this article is to establish whether pretreatment (18)F-FDG uptake predicts disease-free survival (DFS) and overall survival in patients with head-and-neck non-squamous cell carcinoma (SCC).
Eighteen patients (six women and 12 men; mean [± SD] age at diagnosis, 57.89 ± 13.54 years) with head-and-neck non-SCC were included. Tumor FDG uptake was measured by the maximum standardized uptake value (SUV(max)) and was corrected for background liver FDG uptake to derive the corrected SUV(max). Receiver operating characteristic analyses were used to predict the optimal corrected SUV(max) cutoffs for respective outcomes of DFS (i.e., absence of recurrence) and death.
The mean corrected SUV(max) of the 18 head-and-neck tumors was 5.63 ± 3.94 (range, 1.14-14.29). The optimal corrected SUV(max) cutoff for predicting DFS and overall survival was 5.79. DFS and overall survival were significantly higher among patients with corrected SUV(max) < 6 than among patients with corrected SUV(max) ≥ 6. The mean DFS for patients with corrected SUV(max) < 6 was 25.7 ± 11.14 months, and the mean DFS for patients with corrected SUV(max) ≥ 6 was 7.88 ± 7.1 months (p < 0.018). Among patients with corrected SUV(max) < 6, none died, and the mean length of follow-up for this group was 35.2 ± 9.96 months. All of the patients who died had corrected SUV(max) ≥ 6, and the overall survival for this group was 13.28 ± 12.89 months (p < 0.001).
FDG uptake, as measured by corrected SUV(max), may be a predictive imaging biomarker for DFS and overall survival in patients with head-and-neck non-SCC.
本文旨在确定头颈部非鳞状细胞癌(SCC)患者的预处理 18F-FDG 摄取是否可预测无病生存(DFS)和总生存。
纳入 18 例头颈部非 SCC 患者(6 例女性,12 例男性;诊断时的平均[±标准差]年龄为 57.89 ± 13.54 岁)。肿瘤 FDG 摄取通过最大标准化摄取值(SUV(max))来测量,并通过校正背景肝 FDG 摄取来校正 SUV(max),从而得出校正 SUV(max)。使用受试者工作特征分析来预测各自的 DFS(即无复发)和死亡结果的最佳校正 SUV(max)截断值。
18 个头颈部肿瘤的平均校正 SUV(max)为 5.63 ± 3.94(范围为 1.14-14.29)。预测 DFS 和总生存的最佳校正 SUV(max)截断值为 5.79。校正 SUV(max) < 6 的患者的 DFS 和总生存显著高于校正 SUV(max)≥6 的患者。校正 SUV(max) < 6 的患者的平均 DFS 为 25.7 ± 11.14 个月,校正 SUV(max)≥6 的患者的平均 DFS 为 7.88 ± 7.1 个月(p < 0.018)。校正 SUV(max) < 6 的患者中无人死亡,该组的平均随访时间为 35.2 ± 9.96 个月。所有死亡患者的校正 SUV(max)≥6,该组的总生存率为 13.28 ± 12.89 个月(p < 0.001)。
校正 SUV(max)测量的 FDG 摄取可能是头颈部非 SCC 患者 DFS 和总生存的预测性成像生物标志物。