首页> 外文期刊>European Journal of Nuclear Medicine and Molecular Imaging >Imaging of proliferation with 18F-FLT PET/CT versus 18F-FDG PET/CT in non-small-cell lung cancer.
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Imaging of proliferation with 18F-FLT PET/CT versus 18F-FDG PET/CT in non-small-cell lung cancer.

机译:非小细胞肺癌中18F-FLT PET / CT与18F-FDG PET / CT相比的增殖成像。

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PURPOSE: To compare the diagnostic efficacies of (18)F-FLT and (18)F-FDG PET/CT in non-small-cell lung cancer (NSCLC), focusing on the correlation between FLT and FDG tumour uptake and tumour cell proliferation as indicated by the cyclin D1 labelling index. METHODS: A total of 31 patients with NSCLC underwent FLT and FDG PET/CT scanning followed by surgery. PET/CT images were compared with the pathology. Tumour cell proliferation was assessed by cyclin D1 immunohistochemistry. RESULTS: The sensitivities of FLT and FDG PET/CT for the primary lesion were 74% and 94%, respectively (p=0.031). For N staging, 77% patients were correctly staged, 6% overstaged, 16% understaged by FLT, while the values for FDG were 77%, 16% and 6%, respectively. The sensitivity, specificity, accuracy, and positive predictive value with FLT for lymph nodes were 65%, 98%, 93% and 89%, respectively, and 85%, 84%, 84% and 52% with FDG (p<0.01).Tumour SUV of FLT was significantly correlated with the cyclin D1 labelling index (r=0.644; p<0.01), but the SUV of FDG was not significantly correlated (r=0.293; p>0.05). CONCLUSION: In terms of N staging, FLT PET/CT resulted in understaging of more patients but overstaging of fewer patients, and for regional lymph nodes showed better specificity, accuracy and positive predictive value than FDG PET/CT in NSCLC. Tumour FLT uptake was correlated with tumour cell proliferation as indicated by the cyclin D1 labelling index, suggesting that further studies are needed to evaluate the use of FLT PET/CT for the assessment of therapy response to anticancer drugs.
机译:目的:比较(18)F-FLT和(18)F-FDG PET / CT在非小细胞肺癌(NSCLC)中的诊断效果,重点研究FLT和FDG肿瘤摄取与肿瘤细胞增殖之间的相关性如细胞周期蛋白D1标记指数所示。方法:总共31例NSCLC患者接受了FLT和FDG PET / CT扫描,然后进行了手术。将PET / CT图像与病理结果进行比较。通过细胞周期蛋白D1免疫组织化学评估肿瘤细胞增殖。结果:FLT和FDG PET / CT对原发灶的敏感性分别为74%和94%(p = 0.031)。对于N分期,FLT正确分期的患者为77%,超期的患者为6%,低位的患者为16%,而FDG的值分别为77%,16%和6%。 FLT对淋巴结的敏感性,特异性,准确性和阳性预测值分别为FDG的65%,98%,93%和89%,FDG的敏感性为85%,84%,84%和52%(p <0.01) FLT的肿瘤SUV与细胞周期蛋白D1标记指数显着相关(r = 0.644; p <0.01),而FDG的SUV则无显着相关(r = 0.293; p> 0.05)。结论:就N分期而言,FLT PET / CT导致NSCLC患者分期减少但患者分期过多,并且对于局部淋巴结的特异性,准确性和阳性预测价值均高于FDG PET / CT。细胞周期蛋白D1标记指数表明,肿瘤FLT的摄取与肿瘤细胞的增殖相关,这表明需要进一步的研究来评估FLT PET / CT在评估抗癌药物治疗反应中的应用。

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