Mankoff David A, Dunnwald Lisa K, Gralow Julie R, Ellis Georgiana K, Schubert Erin K, Charlop Aaron W, Tseng Jeffrey, Rinn Kristine J, Livingston Robert B
Division of Nuclear Medicine, University of Washington, Seattle, WA, USA.
Nucl Med Biol. 2002 Oct;29(7):719-27. doi: 10.1016/s0969-8051(02)00333-5.
To determine the influence of breast tumor blood flow on MIBI kinetics, we compared MIBI uptake and washout to [O-15]-water PET estimates of blood flow in patients with locally advanced breast cancer.
Prior to therapy, 37 patients underwent MIBI and [O-15]-water PET imaging; 22/37 also had MIBI washout analysis. Twenty-five patients underwent serial imaging over the course of chemotherapy.
MIBI uptake and blood flow had a significant positive correlation pre-therapy. The change in MIBI uptake over the course of therapy also correlated with the change in blood flow. The half-time of MIBI washout inversely correlated with blood flow, indicating faster MIBI washout with higher blood flow.
Blood flow strongly influences early MIBI uptake and can be a factor affecting the rate of MIBI washout in breast tumors. We present a model of MIBI kinetics in tumors which forms a hypothesis for further mechanistic studies of MIBI uptake and washout in breast cancer.
为了确定乳腺肿瘤血流对MIBI动力学的影响,我们比较了局部晚期乳腺癌患者的MIBI摄取和洗脱情况与用[O-15] -水PET估算的血流情况。
在治疗前,37例患者接受了MIBI和[O-15] -水PET成像;37例中的22例还进行了MIBI洗脱分析。25例患者在化疗过程中接受了系列成像检查。
治疗前MIBI摄取与血流呈显著正相关。治疗过程中MIBI摄取的变化也与血流的变化相关。MIBI洗脱的半衰期与血流呈负相关,表明血流越高,MIBI洗脱越快。
血流强烈影响早期MIBI摄取,并且可能是影响乳腺肿瘤中MIBI洗脱速率的一个因素。我们提出了一个肿瘤中MIBI动力学模型,该模型为进一步对乳腺癌中MIBI摄取和洗脱进行机制研究形成了一个假设。