[18-F] 2-氟- 2-脱氧葡萄糖(FDG PET)正电子发射断层扫描在转移性肾细胞癌中的肿瘤负荷评估

Tim Akhurst MD , Vivian Ng MD , Steven M. Larson MD , Joseph A. O'Donoghue PhD , Jayne O'Neel CNMT , Yusuf Erdi PhD , Chaitanya R. Divgi MD
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引用次数: 29

摘要

目的:在晚期癌症患者中,肿瘤总负荷影响肿瘤反应的可能性,对预后具有重要意义。本研究的目的是选择最佳的2-[F-18]氟-2-脱氧-d -葡萄糖-正电子发射断层扫描(FDG PET)肿瘤摄取参数,以准确测量晚期转移性肾细胞癌的肿瘤负荷,并与计算机断层扫描(CT)测量的体积进行比较,作为参考测试。材料与方法:对6例转移性肾细胞癌的CT表现进行分析。所有患者在进入I-II期放射免疫治疗试验前4周内进行CT和FDG PET扫描。基于ct的疾病范围评估(肿瘤体积)和4项基于pet的测量(标准化摄取值[SUVmax]、SUVav、体积和病变总糖酵解[TLG])由放射科医生(VN)和核医学医师(TA)独立完成。然后确定常规(CT)疾病范围与描述FDG肿瘤浓度的参数之间的相关性程度。结果:对6例患者的肺、腹部和头皮的57个ct可测量转移灶进行了评估。对于大于5 cm3的病变,CT和FDG - PET体积估计值之间存在高度相关性。然而,体现FDG摄取和病变大小的PET衍生参数TLG与ct衍生的肿瘤体积的相关性优于单独的FDG PET体积。结论:以CT体积为金标准,以pet为基础估计转移性肾癌患者总肿瘤负荷的最佳方法是病灶总糖酵解的总和。
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Tumor Burden Assessment with Positron Emission Tomography with [18-F] 2-fluoro 2-deoxyglucose (FDG PET) Modeled in Metastatic Renal Cell Cancer

Objective: In patients with advanced cancer, total tumor burden affects the likelihood of tumor response and has important implications for prognosis. The aim of this study was to select the optimum 2-[F-18]fluoro-2-deoxy-D-glucose-positron emission tomography (FDG PET) tumor uptake parameter to accurately measure tumor burden in advanced metastatic renal cell cancer, in comparison with volumes measured with computed tomography (CT), as a reference test.

Materials and Methods: Six patients with metastatic renal cell carcinoma measurable on CT were studied. CT and FDG PET scans were carried out on all patients within 4 weeks prior to their entry into a phase I–II radioimmunotherapy trial. CT-based evaluation of disease extent (tumor volume) and 4 PET-based measurements (standardized uptake value[SUVmax], SUVav, volume, and total lesion glycolysis [TLG]) were performed independently by a radiologist (VN) and a nuclear medicine physician (TA). The degree of correlation between conventional (CT) extent of disease and parameters describing tumor concentration of FDG was then determined.

Results: Fifty-seven CT-measurable metastatic lesions in lung, abdomen, and scalp were evaluated in 6 patients. There was a high correlation between CT and FDG PET volume estimates for lesions greater than 5 cm3 in size. However, a PET-derived parameter that embodies both FDG uptake and lesion size, the TLG, correlated better with CT-derived tumor volume than did FDG PET volume alone.

Conclusion: Using CT volume as a gold standard, the optimal PET-based estimate of total tumor burden in patients with metastatic renal cancer is the sum over all lesions of the total lesion glycolysis.

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