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正电子发射断层扫描评估立体定向体部放疗治疗非小细胞肺癌后局部失败。

Positron emission tomography for assessing local failure after stereotactic body radiotherapy for non-small-cell lung cancer.

机构信息

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

出版信息

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.

Abstract

PURPOSE

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).

METHODS AND MATERIALS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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)。

方法和材料

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。

结果

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%。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e37a/3474601/ef6dbe29f67e/nihms407150f1.jpg

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