Abolmaali N, Haase R, Koch A, Zips D, Steinbach J, Baumann M, Kotzerke J, Zöphel K
OncoRay-Molecular and Biological Imaging, National Center for Radiation Research in Oncology, Institut und Poliklinik für Radiologische Diagnostik, Medical Faculty and University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Nuklearmedizin. 2011;50(1):22-7. doi: 10.3413/nukmed-00328-10-07. Epub 2010 Dec 17.
[¹⁸F]Fluoromisonidazole positron emission tomography (FMISO-PET) is a non invasive imaging technique that can assist detecting intra tumour regions of hypoxia. FMISO-PET evinces comparatively low signal-to-noise-ratio (SNR) and may be acquired dynamically or after different uptake times post injection (p.i.). The aim of this study was to identify, if static images acquired two hours (MISO2) or four hours (MISO4) p.i. reveal higher contrast.
PATIENTS, METHODS: As part of a prospective trial, 23 patients with cancers of the head and neck underwent [¹⁸F]fluorodeoxyglucose (FDG) PET before and during curative radiochemotherapy. Additionally, FMISO-PET studies 2 h and 4 h p.i. were done before treatment and after a mean dose of 11Gy, 23 Gy and 57 Gy during RCT. After coregistration, a dedicated software was used to define the gross tumour volume (GTV) by FDG PET for the primary tumour. This volume was overlaid to the FMISO images and hypoxia within the GTV was determined. The contrast between hypoxia determined by MISO2 and by MISO4 was investigated and analysed with the Wilcoxon-matched-pairs test.
Mean SUVmax in tumours of all examinations was 2.2 (stdev: 0.4, min: 1.3, max: 3.4) after 2 h and 2.4 (stdev: 0.7, min: 1.1, max: 4.4) after 4 h. In the neck musculature the mean SUVmax was 1.5 at both time points and the mean SUVmean decreased from 1.2 after 2 h to 1.1 after 4 h, respectively. These effects resulted in significantly rising contrast ratios from MISO2 to MISO4. The differently defined contrasts revealed significantly higher values for examinations 4 h p.i. (p < 0.002).
Data acquisition of [¹⁸F]FMISO should be done 4 h p.i. to gather the optimal contrast, preferably allowing further analysis, e. g. hypoxic sub volume definition for therapy planning.
[¹⁸F]氟米索硝唑正电子发射断层扫描(FMISO-PET)是一种非侵入性成像技术,可辅助检测肿瘤内的缺氧区域。FMISO-PET的信噪比(SNR)相对较低,可在注射后(p.i.)动态采集或在不同摄取时间后采集。本研究的目的是确定注射后两小时(MISO2)或四小时(MISO4)采集的静态图像是否具有更高的对比度。
患者、方法:作为一项前瞻性试验的一部分,23例头颈部癌症患者在根治性放化疗前及期间接受了[¹⁸F]氟脱氧葡萄糖(FDG)PET检查。此外,在治疗前以及在根治性放化疗期间平均剂量达到11Gy、23Gy和57Gy后,分别进行了注射后2小时和4小时的FMISO-PET研究。在图像配准后,使用专用软件通过FDG PET为原发性肿瘤定义大体肿瘤体积(GTV)。将该体积叠加到FMISO图像上,并确定GTV内的缺氧情况。采用Wilcoxon配对检验研究并分析MISO2和MISO4所确定的缺氧之间的对比度。
所有检查中肿瘤的平均SUVmax在2小时后为2.2(标准差:0.4,最小值:1.3,最大值:3.4),4小时后为2.4(标准差:0.7,最小值:1.1,最大值:4.4)。在颈部肌肉组织中,两个时间点的平均SUVmax均为1.5,平均SUVmean分别从2小时后的1.2降至4小时后的1.1。这些效应导致从MISO2到MISO4的对比度显著提高。不同定义的对比度显示注射后4小时检查的值显著更高(p < 0.002)。
[¹⁸F]FMISO的数据采集应在注射后4小时进行,以获得最佳对比度,最好能允许进一步分析,例如为治疗计划定义缺氧亚体积。