马一栋,胡漫,卢洁,孙晓蓉,付正,尚东平,马莉,赵书强,郑劲松,韩安勤,马长生,于金明.双示踪剂PET-CT在头颈部肿瘤生物适形调强放疗的初步研究[J].中华放射医学与防护杂志,2014,34(8):601-605
双示踪剂PET-CT在头颈部肿瘤生物适形调强放疗的初步研究
Preliminary investigation of 18F-FDG and 18F-FETNIM PET-CT applied in head and neck cancer patients undergoing biological intensity modulated radiotherapy
投稿时间:2013-12-15  
DOI:10.3760/cma.j.issn.0254-5098.2014.08.010
中文关键词:  头颈部肿瘤  18F-脱氧葡萄糖-正电子发射体层显像  18F-赤硝基咪唑-正电子发射体层显像  生物调强放射治疗
英文关键词:Head and neck cancer  18F-FDG PET-CT  18F-FETNIM PET-CT  Biological intensity modulated radiotherapy
基金项目:
作者单位E-mail
马一栋 037009 山西省大同市第五人民医院肿瘤科  
胡漫 山东省放射肿瘤学重点实验室 山东省肿瘤医院放疗科  
卢洁 山东省放射肿瘤学重点实验室 山东省肿瘤医院放疗科  
孙晓蓉 山东省放射肿瘤学重点实验室 山东省肿瘤医院PET/CT中心  
付正 山东省放射肿瘤学重点实验室 山东省肿瘤医院PET/CT中心  
尚东平 山东省放射肿瘤学重点实验室 山东省肿瘤医院放疗科  
马莉 山东省放射肿瘤学重点实验室 山东省肿瘤医院PET/CT中心  
赵书强 山东省放射肿瘤学重点实验室 山东省肿瘤医院PET/CT中心  
郑劲松 山东省放射肿瘤学重点实验室 山东省肿瘤医院PET/CT中心  
韩安勤 山东省放射肿瘤学重点实验室 山东省肿瘤医院放疗科  
马长生 山东省放射肿瘤学重点实验室 山东省肿瘤医院放疗科  
于金明 山东省放射肿瘤学重点实验室 山东省肿瘤医院放疗科 sdyujinming@126.com 
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中文摘要:
      目的 探讨18F-脱氧葡萄糖(18F-FDG)和18F-赤硝基咪唑(18F-FETNIM)双示踪剂PET-CT确定头颈部肿瘤生物适形调强放射治疗(BIMRT)靶区的可行性。方法 经病理证实且未经治疗的头颈部肿瘤患者12例,治疗前行CT模拟定位扫描、18F-FDG PET-CT和18F-FETNIM PET-CT扫描,分别勾画大体肿瘤靶区(GTVCT)、葡萄糖代谢亚靶区(GTVFDG)、乏氧亚靶区(GTVFETNIM),测量并比较原发肿瘤和转移性淋巴结体积,分别表示为GTVP-CT、GTVN-CT、GTVP-FDG、GTVN-FDG、GTVP-FETNIM 和GTVN-FETNIM 结果 12例患者原发肿瘤和转移淋巴结均摄取18F-FDG,SUVmax-P和SUVmax-N分别为12.3±5.5和 5.1±2.8。9例患者原发肿瘤摄取18F-FETNIM,其中5例患者转移性淋巴结有摄取,未见摄取4例;3例患者原发肿瘤未见18F-FETNIM 摄取,其中转移性淋巴结有摄取1例,未见摄取2例。GTVP-CT、GTVP-FDG 和GTVP-FETNIM分别为 (22.23±12.11)、(20.83±11.59)和(1.98±1.81)cm3,GTVN-CT、GTVN-FDG 和GTVN-FETNIM分别为 (10.77±8.87)、(10.41±8.61)和(0.61±1.08)cm3。GTVP-FETNIM < GTVP-CT,GTVP-FETNIM < GTVP-FDG,GTVN-FETNIM < GTVN-CT,GTVN-FETNIM < GTVN-FDGP<0.01),GTVP-CT与GTVP-FDG、GTVN-CT与GTVN-FDG差异无统计学意义。结论 不同示踪剂PET-CT显像反映肿瘤细胞不同方面的生物学信息,根据PET-CT影像所显示的示踪剂高摄取区域将肿瘤组织划分为若干个子区域是可行的,为实现生物调强放疗提供了可靠的研究基础。
英文摘要:
      Objective To evaluate the feasibility of using Fluorine-18 fluorodeoxyglucose (18F-FDG) and Fluorine-18 fluoroerythronitroimidazole (18F-FETNIM) in positron emission tomography with computed tomography (PET-CT) to define biological target volume during the biological intensity modulated radiotherapy (BIMRT). Methods Twelve patients with pathologically confirmed head and neck cancer were scanned with CT simulation, 18F-FDG PET-CT and 18F-FETNIM PET-CT respectively before treatment. Three gross target volumes, GTVCT, GTVFDG and GTVFETNIM, were delineated correspondingly with three modalities. The volumes of primary tumor (P-) and metastatic lymph nodes (N-), denoted as GTVP-CT, GTVN-CT, GTVP-FDG, GTVN-FDG, GTVP-FETNIM and GTVN-FETNIM, were compared respectively. Results Both primary tumor and metastatic lymph node of the 12 patients had 18F-FDG uptake, and the average maximal standard uptake values (SUVmax) were 12.3±5.5 and 5.1±2.8, respectively. Positive primary tumor 18F-FETNIM uptake was observed in 9 patients, yet only 5 of whom had positive 18F-FETNIM uptake in lymph node metastases. Three patients had no 18F-FETNIM uptake in the primary tumor, among whom 1 had positive 18F-FETNIM uptake in lymph node metastases. The volumes of GTVP-CT, GTVP-FDG and GTVP-FETNIM were (22.23±12.11), (20.83±11.59) and (1.98±1.81) cm3, respectively. The volumes of GTVN-CT, GTVN-FDG and GTVN-FETNIM were (10.77±8.87), (10.41±8.61) and (0.61±1.08) cm3, respectively. Compared to CT imaging, the volume differences of primary tumor and metastatic lymph nodes shown on 18F-FDG PET-CT imaging were statistically not significant. Compared with CT and 18F-FDG PET-CT, the corresponding volumes were significantly smaller at 18F-FETNIM PET-CT (P<0.01). Conclusions The study demonstrated that PET-CT imaging using different tracers may define subregions of the tumor for biological target volume delineation, which provides foundations for BIMRT.
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