Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Int J Radiat Oncol Biol Phys. 2012 Aug 1;83(5):1558-65. doi: 10.1016/j.ijrobp.2011.10.035. Epub 2012 May 7.
We analyzed whether positron emission tomography (PET)/computed tomography standardized uptake values (SUVs) after stereotactic body radiotherapy (SBRT) could predict local recurrence (LR) in non-small-cell lung cancer (NSCLC).
This study comprised 128 patients with Stage I (n = 68) or isolated recurrent/secondary parenchymal (n = 60) NSCLC treated with image-guided SBRT to 50 Gy over 4 consecutive days; prior radiotherapy was allowed. PET/computed tomography scans were obtained before therapy and at 1 to 6 months after therapy, as well as subsequently as clinically indicated. Continuous variables were analyzed with Kruskal-Wallis tests and categorical variables with Pearson chi-square or Fisher exact tests. Actuarial local failure rates were calculated with the Kaplan-Meier method.
At a median follow-up of 31 months (range, 6-71 months), the actuarial 1-, 2-, and 3-year local control rates were 100%, 98.5%, and 98.5%, respectively, in the Stage I group and 95.8%, 87.6%, and 85.8%, respectively, in the recurrent group. The cumulative rates of regional nodal recurrence and distant metastasis were 8.8% (6 of 68) and 14.7% (10 of 68), respectively, for the Stage I group and 11.7% (7 of 60) and 16.7% (10 of 60), respectively, for the recurrent group. Univariate analysis showed that SUVs obtained 12.1 to 24 months after treatment for the Stage I group (p = 0.007) and 6.1 to 12 months and 12.1 to 24 months after treatment for the recurrent group were associated with LR (p < 0.001 for both). Of the 128 patients, 17 (13.3%) had ipsilateral consolidation after SBRT but no elevated metabolic activity on PET; none had LR. The cutoff maximum SUV of 5 was found to have 100% sensitivity, 91% specificity, a 50% positive predictive value, and a 100% negative predictive value for predicting LR.
PET was helpful for distinguishing SBRT-induced consolidation from LR. SUVs obtained more than 6 months after SBRT for NSCLC were associated with local failure. A maximum SUV greater than 5, especially at more than 6 months after SBRT, should prompt biopsy to rule out LR.
我们分析了立体定向体部放射治疗(SBRT)后正电子发射断层扫描(PET)/计算机断层扫描标准化摄取值(SUVs)是否可预测非小细胞肺癌(NSCLC)的局部复发(LR)。
这项研究纳入了 128 例 I 期(n=68)或孤立性复发/继发性实质(n=60)NSCLC 患者,这些患者接受了图像引导的 SBRT 治疗,50 Gy 剂量分 4 天给予;允许有既往放疗史。在治疗前、治疗后 1 至 6 个月以及临床需要时进行 PET/计算机断层扫描检查。采用 Kruskal-Wallis 检验分析连续变量,采用 Pearson 卡方检验或 Fisher 确切概率法分析分类变量。采用 Kaplan-Meier 法计算局部失败的累积发生率。
在中位随访 31 个月(范围 6-71 个月)时,I 期组的 1 年、2 年和 3 年局部控制率分别为 100%、98.5%和 98.5%,复发组分别为 95.8%、87.6%和 85.8%。I 期组的区域淋巴结复发和远处转移的累积发生率分别为 8.8%(6/68)和 14.7%(10/68),复发组分别为 11.7%(7/60)和 16.7%(10/60)。单因素分析显示,I 期组治疗后 12.1-24 个月(p=0.007)和复发组治疗后 6.1-12 个月及 12.1-24 个月的 SUVs 与 LR 相关(两者均 p<0.001)。128 例患者中,17 例(13.3%)在 SBRT 后出现同侧实变,但 PET 无代谢活性升高;这些患者均无 LR。发现最大 SUV 为 5 时,对预测 LR 的灵敏度为 100%、特异性为 91%、阳性预测值为 50%、阴性预测值为 100%。
PET 有助于区分 SBRT 诱导的实变与 LR。NSCLC 患者 SBRT 后 6 个月以上获得的 SUVs 与局部失败相关。SUV 大于 5,尤其是 SBRT 后 6 个月以上的 SUV 大于 5,应提示进行活检以排除 LR。