Department of Nuclear Medicine, Henri Becquerel Cancer Center and Rouen University Hospital, France.
Radiother Oncol. 2011 Jan;98(1):109-16. doi: 10.1016/j.radonc.2010.10.011. Epub 2010 Nov 4.
OBJECTIVES: To investigate the changes in tumour proliferation (using FLT), metabolism (using FDG), and hypoxia (using F-miso) during curative (chemo-) radiotherapy (RT) in patients with non-small-cell lung cancer (NSCLC). PATIENTS AND METHODS: Thirty PET scans were performed in five patients (4 males, 1 female) that had histological proof of NSCLC and were candidates for curative-intent RT. Three PET-CT (Biograph S16, Siemens) scans were performed before (t(0)) and during (around dose 46 Gy, t(46)) RT with minimal intervals of 48 h between each PET-CT scan. The tracers used were (18)fluoro-2deoxyglucose (FDG) for metabolism, (18)fluorothymidine (FLT) for proliferation, and (18)F-misonidasole (F-miso) for hypoxia. The 3 image sets obtained at each time point were co-registered (rigid: n=9, elastic: n=1, Leonardo, TrueD, Siemens) using FDG PET-CT as reference. VOIs were delineated (40% SUV(max) values were used as a threshold) for tumours and lymph nodes on FDG PET-CT, and they were automatically pasted on FLT and F-miso PET-CT images. ANOVA and correlation analyses were used for comparison of SUV(max) values. RESULTS: Four tumours and twelve nodes were identified on initial FDG PET-CT images. FLT SUV(max) values were significantly lower (p<0.0006) at t(46) in both tumours and nodes. The decrease in FDG SUV(max) values had a trend towards significance (p=0.048). F-Miso SUV(max) values were significantly higher in tumours than in nodes (p=0.02) and did not change during radiotherapy (p=0.39). A significant correlation was observed between FLT and FDG uptake (r=0.56, p<10(-4)) when all data were pooled together, and they remained similar when the before and during RT data were analysed separately. FDG and F-miso uptakes were significantly correlated (r=0.59, p=0.0004) when all data were analysed together. The best fit was obtained after adjusting for lesion type (tumour vs. node). This correlation was observed for the SUV(max) measured during RT (r=0.70, p=0.008) but not for the pre-RT data (r=0.19, p=0.35). The weak correlation between FLT and F-miso uptakes only became significant (r=0.66, p=0.002) when the analysis was restricted to the data acquired during RT. CONCLUSION: Three different PET acquisitions can be performed quasi-simultaneously (4-7 days) before and during radiotherapy in patients with NSCLC. Our results at 46 Gy suggest that a fast decrease in the proliferation of both tumours and nodes exists during radiotherapy with differences in metabolism (borderline significant decrease) and hypoxia (stable).
目的:研究非小细胞肺癌 (NSCLC) 患者在接受根治性(化疗)放疗 (RT) 过程中肿瘤增殖(使用 FLT)、代谢(使用 FDG)和缺氧(使用 F-miso)的变化。 方法:对 5 名经组织学证实患有 NSCLC 且有根治性意向 RT 适应证的患者进行了 30 次 PET 扫描。在 RT 期间(约 46 Gy 时,t(46)) 进行了 3 次 PET-CT(Biograph S16,西门子)扫描,每次 PET-CT 扫描之间的间隔最小为 48 小时。使用的示踪剂包括代谢用 (18)氟-2-脱氧葡萄糖 (FDG)、增殖用 (18)氟胸腺嘧啶 (FLT) 和缺氧用 (18)氟米索硝唑 (F-miso)。使用 FDG PET-CT 作为参考,使用 (18)FLT 和 F-miso PET-CT 图像对每个时间点获得的 3 个图像集进行刚性(n=9)和弹性(n=1,Leonardo、TrueD、西门子)配准。在 FDG PET-CT 上为肿瘤和淋巴结勾画 VOI(使用 40% SUV(max) 值作为阈值),并自动将其粘贴到 FLT 和 F-miso PET-CT 图像上。使用 ANOVA 和相关性分析比较 SUV(max) 值。 结果:在初始 FDG PET-CT 图像上识别出 4 个肿瘤和 12 个淋巴结。在 t(46) 时,肿瘤和淋巴结的 FLT SUV(max) 值均显著降低(p<0.0006)。FDG SUV(max) 值的降低有统计学意义(p=0.048)。肿瘤的 F-Miso SUV(max) 值明显高于淋巴结(p=0.02),且在放疗期间无变化(p=0.39)。当所有数据汇总在一起时,FLT 和 FDG 摄取之间观察到显著相关性(r=0.56,p<10(-4)),当分别分析 RT 前后的数据时,相关性仍相似。FDG 和 F-miso 摄取之间存在显著相关性(r=0.59,p=0.0004),当所有数据一起分析时。最佳拟合是在调整病变类型(肿瘤与淋巴结)后获得的。这种相关性在 RT 期间测量的 SUV(max) 时观察到(r=0.70,p=0.008),但在 RT 前数据中观察不到(r=0.19,p=0.35)。FLT 和 F-miso 摄取之间的弱相关性仅在限制为 RT 期间获得的数据时才变得显著(r=0.66,p=0.002)。 结论:在 NSCLC 患者中,在放疗前和放疗期间可以近乎同时进行三次不同的 PET 采集(4-7 天)。我们在 46 Gy 时的结果表明,肿瘤和淋巴结的增殖在放疗期间迅速下降(存在差异,代谢(有边缘显著下降)和缺氧(稳定)。
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