首页> 外文期刊>Clinical nuclear medicine >Potential role of FDG PET imaging in predicting metastatic potential and assessment of therapeutic response to neoadjuvant chemotherapy in Ewing sarcoma family of tumors.
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Potential role of FDG PET imaging in predicting metastatic potential and assessment of therapeutic response to neoadjuvant chemotherapy in Ewing sarcoma family of tumors.

机译:FDG PET成像在预测尤因肉瘤家族肿瘤中的转移潜力和评估对新辅助化疗的治疗反应中的潜在作用。

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AIMS AND OBJECTIVES: The aim of this study was to retrospectively correlate FDG uptake in primary Ewing sarcoma family of tumors (ESFT) with tumor behavior, and to evaluate whether FDG PET can be used to predict response to neoadjuvant chemotherapy (NACT) in this patient group. METHODS: Out of the total 54 patients of recently diagnosed ESFT who underwent pretreatment FDG PET imaging, group I included patients without metastasis at presentation (n = 34) and group II included those with metastasis at presentation (n = 20). Fourteen of these patients had undergone FDG PET after 4 cycles of induction chemotherapy and surgical resection of primary tumor. In this subgroup of 14 patients, maximum standardized uptake value (SUVmax) of primary tumor was estimated before and after 4 cycles of induction chemotherapy and was correlated with the histopathological response in terms of necrosis in the tumor specimen. RESULTS: Mean SUVmax in the primary tumor in group I patients was 6.84 and in group II patients, it was 11.31. The difference between mean SUVmax of these 2 groups was significant by Wilcoxon test analysis, with P < 0.01. In group II patients, SUVmax in metastasis with maximum FDG uptake was consistently lower as compared with that of primary tumor. In subgroup of 14 patients, Pearson correlation analysis showed that percentage change in SUVmax of primary tumor correlated well with percentage necrosis on histopathological examination (P < 0.01). CONCLUSION: FDG uptake in primary ESFT reflected its metastatic potential and hence the aggressive behavior. The significant correlation between change in metabolic activity of the primary tumor and histopathological response after neoadjuvant chemotherapy suggests that FDG PET may be an ideal noninvasive method to assess tumor behavior and response to therapy in ESFT.
机译:目的和目的:本研究的目的是回顾性地将原发性尤因肉瘤家族(ESFT)的FDG摄取与肿瘤行为相关联,并评估FDG PET是否可用于预测该患者对新辅助化疗(NACT)的反应组。方法:在54例近期诊断为ESFT的接受FDG PET显像术治疗的患者中,第一组包括就诊时无转移的患者(n = 34),第二组包括就诊时有转移的患者(n = 20)。这些患者中有14位在诱导化疗和原发肿瘤手术切除4个周期后接受了FDG PET。在这14例患者的亚组中,在诱导化疗的4个周期之前和之后估计了原发肿瘤的最大标准摄取值(SUVmax),并且就肿瘤标本的坏死而言与组织病理学反应相关。结果:第一组患者原发肿瘤的平均SUVmax为6.84,第二组患者为11.31。通过Wilcoxon检验分析,这两组的平均SUVmax之间的差异是显着的,P <0.01。在第二组患者中,具有最大FDG摄取的转移中的SUVmax与原发性肿瘤相比始终较低。在14例患者的亚组中,Pearson相关分析表明,在组织病理学检查中,原发性肿瘤SUVmax的百分比变化与坏死百分比具有很好的相关性(P <0.01)。结论:原发性ESFT摄取FDG反映了其转移潜能,因此具有侵略性。新辅助化疗后,原发肿瘤代谢活性的变化与组织病理学反应之间的显着相关性表明,FDG PET可能是评估肿瘤行为和对ESFT的治疗反应的理想无创方法。

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