Division of Nuclear Medicine, University of Washington and Seattle Cancer Care Alliance, Seattle, Washington 98195-7987, USA.
J Nucl Med. 2010 Apr;51(4):521-7. doi: 10.2967/jnumed.109.070052. Epub 2010 Mar 17.
The most common site of metastasis for breast cancer is bone. Quantitative (18)F-fluoride PET can estimate the kinetics of fluoride incorporation into bone as a measure of fluoride transport, bone formation, and turnover. The purpose of this analysis was to evaluate the accuracy and precision of (18)F-fluoride model parameter estimates for characterizing regional kinetics in metastases and normal bone in breast cancer patients.
Twenty metastatic breast cancer patients underwent dynamic (18)F-fluoride PET. Mean activity concentrations were measured from serial blood samples and regions of interest placed over bone metastases, normal vertebrae, and cardiac blood pools. This study examined parameter identifiability, model sensitivity, error, and accuracy using parametric values from the patient cohort.
Representative time-activity curves and model parameter ranges were obtained from the patient cohort. Model behavior analyses of these data indicated (18)F-fluoride transport and flux (K(1) and Ki, respectively) into metastatic and normal osseous tissue could be independently estimated with a reasonable bias of 9% or less and reasonable precision (coefficients of variation <or= 16%). Average (18)F-fluoride transport and flux into metastases from 20 patients (K(1) = 0.17 +/- 0.08 mL x cm(-3) x min(-1) and Ki = 0.10 +/- 0.05 mL x cm(-3) x min(-1)) were both significantly higher than for normal bone (K(1) = 0.09 +/- 0.03 mL x cm(-3) x min(-1) and Ki = 0.05 +/- 0.02 mL x cm(-3) x min(-1), P < 0.001).
Fluoride transport and flux can be accurately and independently estimated for bone metastases and normal vertebrae. Reasonable bias and precision for estimates of K(1) and Ki from simulations and significant differences in values from patient modeling results in metastases and normal bone suggest that (18)F-fluoride PET images may be useful for assessing changes in bone turnover in response to therapy. Future studies will examine the correlation of parameters to biologic features of bone metastases and to response to therapy.
乳腺癌最常见的转移部位是骨骼。定量(18)F-氟化物 PET 可以估计氟化物掺入骨骼的动力学,作为氟化物转运、骨形成和转换的测量。本分析的目的是评估(18)F-氟化物模型参数估计在乳腺癌患者骨转移和正常骨中区域动力学特征中的准确性和精密度。
20 例转移性乳腺癌患者接受了动态(18)F-氟化物 PET。从连续的血样中测量平均放射性浓度,并在骨转移、正常椎体和心脏血池中放置感兴趣区。本研究使用患者队列中的参数值检查了参数可识别性、模型敏感性、误差和准确性。
从患者队列中获得了代表性的时间-活性曲线和模型参数范围。对这些数据的模型行为分析表明,转移性和正常骨组织中的(18)F-氟化物转运和通量(分别为 K(1)和 Ki)可以独立估计,其偏差合理,小于或等于 9%,精度合理(变异系数<或=16%)。20 例患者的(18)F-氟化物平均转运和通量(K(1)=0.17±0.08 mL·cm(-3)·min(-1)和 Ki=0.10±0.05 mL·cm(-3)·min(-1))进入转移灶均显著高于正常骨(K(1)=0.09±0.03 mL·cm(-3)·min(-1)和 Ki=0.05±0.02 mL·cm(-3)·min(-1),P<0.001)。
可以准确、独立地估计骨转移和正常椎体的氟化物转运和通量。来自模拟的 K(1)和 Ki 估计值的合理偏差和精度以及来自患者模型结果的转移灶和正常骨中值的显著差异表明,(18)F-氟化物 PET 图像可能有助于评估治疗对骨转换的影响。未来的研究将检查参数与骨转移的生物学特征以及对治疗的反应之间的相关性。