首页> 外文期刊>The Journal of Nuclear Medicine >Metabolic Evaluation of Non-Small Cell Lung Cancer Patient-Derived Xenograft Models Using 18F-FDG PET: A Potential Tool for Early Therapy Response
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Metabolic Evaluation of Non-Small Cell Lung Cancer Patient-Derived Xenograft Models Using 18F-FDG PET: A Potential Tool for Early Therapy Response

机译:使用18F-FDG PET对非小细胞肺癌患者来源的异种移植模型进行代谢评估:早期治疗反应的潜在工具

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id="p-4">Lung cancer heterogeneity makes response to therapy extremely hard to predict. Patient-derived xenografts (PDXs) are a reliable preclinical model that closely recapitulates the main characteristics of the parental tumors and may represent a useful asset for testing new therapies. Here, using PET imaging, we investigated whether lung cancer PDXs reproduce the metabolic characteristics of the corresponding parental tumors. >Methods: We performed longitudinal 18F-FDG PET studies on 9 different PDX groups obtained by implanting primary-cancer fragments harvested from patients into mice. The SUVmax of each PDX was calculated and compared with the SUVmax of the corresponding parental tumor. >Results: Tumor growth rate and uptake varied among the different PDXs and confirmed the preservation of individual characteristics. The intragroup reproducibility of PET measurements was good. Furthermore, PDXs from tumors with a higher metabolic rate displayed a rank order of uptake similar to that of the parental tumors. >Conclusion: PDXs reproduced the glucose metabolism of the parental tumors and therefore represent a promising preclinical model for the early assessment of therapy efficacy.
机译:id =“ p-4”>肺癌异质性使得对治疗的反应极为难以预测。患者来源的异种移植物(PDXs)是一种可靠的临床前模型,可密切概括亲代肿瘤的主要特征,并且可能代表着测试新疗法的有用资产。在这里,使用PET成像,我们调查了肺癌PDXs是否重现了相应亲本肿瘤的代谢特征。 >方法:我们对9种不同的PDX组进行了纵向 18 F-FDG PET研究,这些9种PDX组是通过将从患者体内收集的原发癌片段植入小鼠体内而获得的。计算每个PDX的SUV max ,并将其与相应亲本肿瘤的SUV max 进行比较。 >结果:肿瘤的生长速率和摄取在不同的PDX中有所不同,并证实了个体特征的保留。 PET测量的组内重现性良好。此外,来自代谢率较高的肿瘤的PDX显示出与亲代肿瘤相似的摄取等级。 >结论:PDX能够复制亲本肿瘤的葡萄糖代谢,因此代表了一种有前途的临床前模型,可用于早期评估治疗效果。

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