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首页> 外文期刊>Radiotherapy and oncology: Journal of the European Society for Therapeutic Radiology and Oncology >Identification of residual metabolic-active areas within individual NSCLC tumours using a pre-radiotherapy (18)Fluorodeoxyglucose-PET-CT scan.
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Identification of residual metabolic-active areas within individual NSCLC tumours using a pre-radiotherapy (18)Fluorodeoxyglucose-PET-CT scan.

机译:使用放疗前(18)Fluorodeoxyglucose-PET-CT扫描鉴定单个NSCLC肿瘤内残留的代谢活性区域。

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BACKGROUND AND PURPOSE: Non-small cell lung cancer (NSCLC) tumours are mostly heterogeneous. We hypothesized that areas within the tumour with a high pre-radiation (18)F-deoxyglucose (FDG) uptake, could identify residual metabolic-active areas, ultimately enabling selective-boosting of tumour sub-volumes. MATERIAL AND METHODS: Fifty-five patients with inoperable stage I-III NSCLC treated with chemo-radiation or with radiotherapy alone were included. For each patient one pre-radiotherapy and one post-radiotherapy FDG-PET-CT scans were available. Twenty-two patients showing persistent FDG uptake in the primary tumour after radiotherapy were analyzed. Overlap fractions (OFs) were calculated between standardized uptake value (SUV) threshold-based auto-delineations on the pre- and post-radiotherapy scan. RESULTS: Patients with residual metabolic-active areas within the tumour had a significantly worse survival compared to individuals with a complete metabolic response (p=0.002). The residual metabolic-active areas within the tumour largely corresponded (OF>70%) with the 50%SUV high FDG uptake area of the pre-radiotherapy scan. The hotspot within the residual area (90%SUV) was completely within the GTV (OF=100%), and had a high overlap with the pre-radiotherapy 50%SUV threshold (OF>84%). CONCLUSIONS: The location of residual metabolic-active areas within the primary tumour after therapy corresponded with the original high FDG uptake areas pre-radiotherapy. Therefore, a single pre-treatment FDG-PET-CT scan allows for the identification of residual metabolic-active areas.
机译:背景与目的:非小细胞肺癌(NSCLC)肿瘤大多是异质性的。我们假设肿瘤中具有高预辐射(18)F-脱氧葡萄糖(FDG)摄取的区域可以识别残留的代谢活性区域,最终使肿瘤亚体积得以选择性增强。材料与方法:纳入了55例不能接受I-III期NSCLC化疗和放疗的患者。对于每位患者,可以进行一次放射治疗和一次放射治疗后的FDG-PET-CT扫描。分析了22例放疗后原发性肿瘤持续摄取FDG的患者。在放疗前和放疗后基于标准化摄取值(SUV)阈值的自动描述之间计算重叠分数(OFs)。结果:与具有完全代谢反应的个体相比,肿瘤内具有残留代谢活性区域的患者的生存期明显较差(p = 0.002)。肿瘤内残留的代谢活性区域与放疗前扫描的50%SUV高FDG摄取区域在很大程度上对应(OF> 70%)。残留区域内的热点(90%SUV)完全位于GTV内(OF = 100%),并且与放疗前50%SUV阈值(OF> 84%)高度重叠。结论:治疗后原发肿瘤内残留的代谢活性区域的位置与放疗前原始的高FDG摄取区域相对应。因此,单次FDG-PET-CT预处理扫描可以识别残留的代谢活性区域。

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