Department of Radiation Oncology, Duke University Medical Center, Durham, NC 27710, USA.
Int J Radiat Oncol Biol Phys. 2012 Feb 1;82(2):548-53. doi: 10.1016/j.ijrobp.2010.11.050. Epub 2011 Jan 27.
To evaluate the prognostic significance of different descriptive parameters in head-and-neck cancer patients undergoing pretreatment [F-18] fluoro-D-glucose-positron emission tomography (FDG-PET) imaging.
Head-and-neck cancer patients who underwent FDG-PET before a course of curative intent radiotherapy were retrospectively analyzed. FDG-PET imaging parameters included maximum (SUV(max)), and mean (SUV(mean)) standard uptake values, and total lesion glycolysis (TLG). Tumors and lymph nodes were defined on co-registered axial computed tomography (CT) slices. SUV(max) and SUV(mean) were measured within these anatomic regions. The relationships between pretreatment SUV(max), SUV(mean), and TLG for the primary site and lymph nodes were assessed using a univariate analysis for disease-free survival (DFS), locoregional control (LRC), and distant metastasis-free survival (DMFS). Kaplan-Meier survival curves were generated and compared via the log-rank method. SUV data were analyzed as continuous variables.
A total of 88 patients was assessed. Two-year OS, LRC, DMFS, and DFS for the entire cohort were 85%, 78%, 81%, and 70%, respectively. Median SUV(max) for the primary tumor and lymph nodes was 15.4 and 12.2, respectively. Median SUV(mean) for the primary tumor and lymph nodes was 7 and 5.2, respectively. Median TLG was 770. Increasing pretreatment SUV(mean) of the primary tumor was associated with decreased disease-free survival (p = 0.01). Neither SUV(max) in the primary tumor or lymph nodes nor TLG was prognostic for any of the clinical endpoints. Patients with pretreatment tumor SUV(mean) that exceeded the median value (7) of the cohort demonstrated inferior 2-year DFS relative to patients with SUV(mean) ≤ the median value of the cohort, 58% vs. 82%, respectively, p = 0.03.
Increasing SUV(mean) in the primary tumor was associated with inferior DFS. Although not routinely reported, pretreatment SUV(mean) may be a useful prognostic FDG-PET parameter and should be further evaluated prospectively.
评估头颈部癌患者接受预处理 [F-18] 氟代-D-葡萄糖正电子发射断层扫描(FDG-PET)成像时不同描述性参数的预后意义。
回顾性分析了接受根治性放疗前接受 FDG-PET 检查的头颈部癌患者。FDG-PET 成像参数包括最大(SUV(max))和平均(SUV(mean))标准摄取值,以及总病变糖酵解(TLG)。肿瘤和淋巴结在同机轴向计算机断层扫描(CT)切片上定义。在这些解剖区域内测量 SUV(max)和 SUV(mean)。使用单变量分析评估原发灶和淋巴结的预处理 SUV(max)、SUV(mean)和 TLG 与无病生存率(DFS)、局部区域控制(LRC)和无远处转移生存率(DMFS)的关系。通过对数秩检验生成 Kaplan-Meier 生存曲线并进行比较。SUV 数据作为连续变量进行分析。
共评估了 88 例患者。整个队列的 2 年 OS、LRC、DMFS 和 DFS 分别为 85%、78%、81%和 70%。原发灶和淋巴结的 SUV(max)中位数分别为 15.4 和 12.2。原发灶和淋巴结的 SUV(mean)中位数分别为 7 和 5.2。TLG 中位数为 770。原发灶 SUV(mean)增加与疾病无进展生存(DFS)降低相关(p=0.01)。原发灶或淋巴结的 SUV(max)和 TLG 均与任何临床终点无关。与 SUV(mean)≤队列中位数的患者相比,预处理肿瘤 SUV(mean)超过队列中位数的患者 2 年 DFS 较差,分别为 58%和 82%,p=0.03。
原发灶 SUV(mean)增加与 DFS 降低相关。尽管未常规报告,但预处理 SUV(mean)可能是一种有用的 FDG-PET 预后参数,应进一步前瞻性评估。