首页> 外文期刊>The Journal of Nuclear Medicine >18F-FDG PET/CT as an Indicator of Progression-Free and Overall Survival in Osteosarcoma.
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18F-FDG PET/CT as an Indicator of Progression-Free and Overall Survival in Osteosarcoma.

机译:18F-FDG PET / CT可作为骨肉瘤无进展生存和总体生存的指标。

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The aim of our study was to retrospectively evaluate whether maximum standardized uptake value (SUV(max)), total lesion gylcolysis (TLG), or change therein using (18)F-FDG PET/CT performed before and after initial chemotherapy were indicators of patient outcome. METHODS: Thirty-one consecutive patients who underwent (18)F-FDG PET/CT before and after chemotherapy, followed by tumor resection, were retrospectively reviewed. Univariate Cox regression was used to analyze for relationships between covariates of interest (SUV(max) before and after chemotherapy, change in SUV(max), TLG before and after chemotherapy, change in TLG, and tumor necrosis) and progression-free and overall survival. Logistic regression was used to evaluate tumor necrosis. RESULTS: High SUV(max) before and after chemotherapy (P = 0.008 and P = 0.009, respectively) was associated with worse progression-free survival. The cut point for SUV(max) before chemotherapy was greater than 15 g/mL* (P = 0.015), and after chemotherapy it was greater than 5 g/mL* (P = 0.006), as measured at our institution and using lean body mass. Increase in TLG after chemotherapy was associated with worse progression-free survival (P = 0.016). High SUV(max) after chemotherapy was associated with poor overall survival (P = 0.035). The cut point was above the median of 3.3 g/mL* (P = 0.043). High TLG before chemotherapy was associated with poor overall survival (P = 0.021). Good overall and progression-free survival was associated with a tumor necrosis greater than 90% (P = 0.018 and 0.08, respectively). A tumor necrosis greater than 90% was most strongly associated with a decrease in SUV(max) (P = 0.015). CONCLUSION: (18)F-FDG PET/CT can be used as a prognostic indicator for progression-free survival, overall survival, and tumor necrosis in osteosarcoma.
机译:我们研究的目的是回顾性评估初始化疗前后最大标准化摄取值(SUV(max)),总病变糖酵解(TLG)或其中的变化是否使用(18)F-FDG PET / CT来指示。患者预后。方法:回顾性分析了连续31例在化疗前后进行(18)F-FDG PET / CT,然后进行肿瘤切除的患者。使用单变量Cox回归分析感兴趣的协变量(化疗前后的SUV(max),SUV(max)的变化,化疗前后的TLG,TLG的变化和肿瘤坏死)与无进展和总体之间的关系生存。 Logistic回归用于评估肿瘤坏死。结果:化疗前后高SUV(最高)(分别为P = 0.008和P = 0.009)与无进展生存期较差有关。根据我们机构和使用瘦肉所测得,化疗前SUV的最大切点大于15 g / mL *(P = 0.015),化疗后大于5 g / mL *(P = 0.006)。身体质量。化疗后TLG的升高与无进展生存期恶化相关(P = 0.016)。化疗后高SUV(max)与总生存期差有关(P = 0.035)。切点高于中位数3.3 g / mL *(P = 0.043)。化疗前高TLG与总生存期差有关(P = 0.021)。良好的总体生存率和无进展生存率与大于90%的肿瘤坏死有关(分别为P = 0.018和0.08)。大于90%的肿瘤坏死与SUV(max)的降低密切相关(P = 0.015)。结论:(18)F-FDG PET / CT可作为骨肉瘤无进展生存期,总体生存期和肿瘤坏死的预后指标。

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