邓红彬,巩贯忠,陈进琥,段敬豪,尹勇.18F-FDG PET/CT引导局部晚期非小细胞肺癌靶区剂量提升的可行性研究[J].中华放射医学与防护杂志,2017,37(10):747-751
18F-FDG PET/CT引导局部晚期非小细胞肺癌靶区剂量提升的可行性研究
The study of the feasibility of dose escalation guided by 18F-FDG PET/CT for high metabolic region in radiotherapy of locally advanced non-small cell lung cancer
投稿时间:2017-04-01  
DOI:10.3760/cma.j.issn.0254-5098.2017.10.005
中文关键词:  剂量提升  非小细胞肺癌  亚区域  18F-FDG PET/CT  放射治疗
英文关键词:Dose escalation  Non-small cell lung cancer  Sub-volume  18F-FDG PET/CT  Radiotherapy
基金项目:国家自然科学基金(81301936,81472811);山东省科技发展计划项目(2014GGC03038)
作者单位E-mail
邓红彬 250022, 济南大学 山东省医学科学院医学与生命科学学院  
巩贯忠 250117 济南, 山东大学附属山东省肿瘤医院放射物理技术科 山东省医学科学院  
陈进琥 250117 济南, 山东大学附属山东省肿瘤医院放射物理技术科 山东省医学科学院  
段敬豪 250117 济南, 山东大学附属山东省肿瘤医院放射物理技术科 山东省医学科学院  
尹勇 250117 济南, 山东大学附属山东省肿瘤医院放射物理技术科 山东省医学科学院 yongyinsd@163.com 
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中文摘要:
      目的 研究基于放疗前正电子发射计算机断层显像(PET/CT)的标准摄取值(SUV)梯度引导局部晚期非小细胞肺癌(NSCLC)患者靶向剂量提升的可行性及剂量学特点。方法 收集29例NSCLC患者的放疗前PET/CT图像,在PET/CT图像上勾画大体肿瘤靶区(GTV),以最大SUV值(SUVmax)的50%和75%为阈值将GTV分割为3个代谢活性亚区域,低于50%SUVmax的区域为GTV1,50%SUVmax到75%SUVmax的区域为GTV2,高于75%SUVmax的区域为GTV3。计划靶区(PTV)、PTV1、PTV2、PTV3分别由GTV、GTV1、GTV2及GTV3外放适当边界得到。计划1:在PTV上照射均匀60 Gy处方剂量。计划2:将PTV1、PTV2和PTV3的处方剂量分别设置为60~66 Gy、66~72 Gy和≥72 Gy。比较两种治疗计划靶区和危及器官(OAR)的剂量学差异。结果 相对于计划1,计划2将2%的PTV体积接受的剂量(D2)由66.5 Gy提升至78.5 Gy,剂量提升约20%;PTV的平均剂量提升了8.9%(63.2~68.8 Gy)、PTV1,PTV2、PTV3的平均剂量分别提升了2.8%(62.7~64.4 Gy)、10.3%(63.5~70.0 Gy)、18.7%(63.8~75.8 Gy)。各亚区域剂量均得到有效提升。计划1与计划2 中PTV的60 Gy剂量线靶区覆盖度基本相当,差异无统计学意义(P>0.05),均匀性指数(HI)的差异有统计学意义(t=23.3, P<0.05),计划2中随着最大剂量的提升,HI下降显著。肺、心脏和脊髓的受照剂量在两个治疗计划中基本相当,差异均无统计学意义(P>0.05)。结论 对不同代谢活性梯度实施差异化的放疗剂量,在不增加危及器官辐射剂量的前提下,可对代谢活性高的亚区域进行靶向剂量提升,具有提高肿瘤局部控制的潜能。
英文摘要:
      Objective To investigate dose escalation by metabolic sub-volume based on standard uptake values (SUV) gradient of pre-treatment positron emission tomography/computed tomography (PET/CT) for locally advanced non-small cell lung cancer (NSCLC) radiotherapy.Methods The pre-treatment 18F-FDG PET/CT images of 29 patients with locally advanced NSCLC were analyzed retrospectively. Gross tumor volume (GTV) was delineated on the PET/CT fusion images. Tumor metabolic sub-volume was segmented according to the threshold of 50% and 75% maximum standard uptake values (SUVmax). The region that under 50% SUVmax was defined as GTV1. From 50% to 75% SUVmax was defined as GTV2,and over 75% SUVmax was defined as GTV3. PTV (planning target volume), PTV1, PTV2 and PTV3 were extended from GTV, GTV1, GTV2 and GTV3, and different plans were designed subsequently. Plan 1 was designed for PTV with prescription dose 60 Gy, and Plan 2 was designed for PTV1, PTV2 and PTV3 with prescription dose 60-66 Gy, 66-72 Gy and ≥ 72 Gy, respectively. The dosimetric parameters between tumor target and organs at risk (OARs) were compared.Results Compared to Plan 1, the absorbed dose in Plan 2 that covers 2% volume of the PTV (D2) was increased from 66.5 Gy to 78.5 Gy and the dose was escalated by about 23.2%. The average dose of PTV1, PTV2 and PTV3 increased by 2.8% (62.7-64.4 Gy), 10.3% (63.5-70.0 Gy), 18.7% (63.8-75.8 Gy), and the average dose of PTV increased by 8.9% (63.2-68.8 Gy). The sub-regional dose had been effectively improved. There was no significant difference in target coverage between Plan 1 and Plan 2 (P>0.05). Homogeneity index(HI) was decreased with the escalation of maximum dose for Plan 2(t=23.3, P<0.05). There was no statistically significant difference in radiation dose of OARs between two plans(P>0.05).Conclusions Dose escalation based on metabolic sub-volume from 18F-FDG PET/CT was feasible, and radiation dose escalation of sub-volume with high metabolic activity can be achieved without increasing the OARs dose.
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