Weber W A, Ziegler S I, Thödtmann R, Hanauske A R, Schwaiger M
Nuklearmedizinsche Klinik, Klinikum Rechts der Isar, Technische Universität München, Germany.
J Nucl Med. 1999 Nov;40(11):1771-7.
PET using 18F-fluorodeoxyglucose (FDG) is increasingly applied to monitor the response of malignant tumors to radiotherapy and chemotherapy. The aim of this study was to assess the reproducibility of serial FDG PET measurements to define objective criteria for the evaluation of treatment-induced changes.
Sixteen patients participating in phase I studies of novel antineoplastic compounds were examined twice by FDG PET within 10 d while they were receiving no therapy. Standardized uptake values (SUVs), FDG net influx constants (Ki), glucose normalized SUVs (SUV(gluc)) and influx constants (K(i,gluc)) were determined for 50 separate lesions. The precision of repeated measurements was determined on a lesion-by-lesion and a patient-by-patient basis.
None of the parameters showed a significant increase or decrease at the two examinations. The differences of repeated measurements were approximately normally distributed for all parameters with an SD of the mean percentage difference of about 10%. The 95% normal ranges for spontaneous fluctuations of SUV, SUV(gluc), Ki and K(i,gluc) were determined to be +/-0.91, +/-1.14, +/-0.52 mL/100 g/min and +/-0.64 mL/100 g/min, respectively. Analysis on a lesion-by-lesion basis yielded similar results.
FDG PET provides several highly reproducible quantitative parameters of tumor glucose metabolism. Changes of a parameter that are outside the 95% normal range determined in this study may be used to define a metabolic response to therapy.
使用18F-氟脱氧葡萄糖(FDG)的正电子发射断层显像(PET)越来越多地应用于监测恶性肿瘤对放疗和化疗的反应。本研究的目的是评估连续FDG PET测量的可重复性,以确定评估治疗引起变化的客观标准。
16名参与新型抗肿瘤化合物I期研究的患者在未接受治疗的情况下,于10天内接受了两次FDG PET检查。对50个独立病灶测定标准化摄取值(SUV)、FDG净流入常数(Ki)、葡萄糖标准化SUV(SUV(gluc))和流入常数(K(i,gluc))。在逐个病灶和逐个患者的基础上确定重复测量的精度。
两次检查时,所有参数均未显示出显著增加或减少。所有参数重复测量的差异近似呈正态分布,平均百分比差异的标准差约为10%。SUV、SUV(gluc)、Ki和K(i,gluc)自发波动的95%正常范围分别确定为±0.91、±1.14、±0.52 mL/100 g/min和±0.64 mL/100 g/min。逐个病灶分析得出了类似结果。
FDG PET提供了几个高度可重复的肿瘤葡萄糖代谢定量参数。超出本研究确定的95%正常范围的参数变化可用于定义对治疗的代谢反应。