TY - JOUR T1 - Mammary Cancer Bone Metastasis Follow-up Using Multimodal Small-Animal MR and PET Imaging JF - Journal of Nuclear Medicine JO - J Nucl Med SP - 944 LP - 952 DO - 10.2967/jnumed.112.114215 VL - 54 IS - 6 AU - Louis Doré-Savard AU - David A. Barrière AU - Élora Midavaine AU - Danny Bélanger AU - Nicolas Beaudet AU - Luc Tremblay AU - Jean-François Beaudoin AU - Eric E. Turcotte AU - Roger Lecomte AU - Martin Lepage AU - Philippe Sarret Y1 - 2013/06/01 UR - http://jnm.snmjournals.org/content/54/6/944.abstract N2 - Despite tremendous progress in the management of breast cancer, the survival rate of this disease is still correlated with the development of metastases—most notably, those of the bone. Diagnosis of bone metastasis requires a combination of multiple imaging modalities. MR imaging remains the best modality for soft-tissue visualization, allowing for the distinction between benign and malignant lesions in many cases. On the other hand, PET imaging is frequently more specific at detecting bone metastasis by measuring the accumulation of radiotracers, such as 18F-sodium fluoride (18F-NaF) and 18F-FDG. Thus, the main purpose of this study was to longitudinally monitor bone tumor progression using PET/MR image coregistration to improve noninvasive imaging–assisted diagnoses. Methods: After surgical implantation of mammary MRMT-1 cells in a rat femur, we performed minimally invasive imaging procedures at different time points throughout tumor development. The procedure consisted of sequential coregistered MR and PET image acquisition, using gadolinium-diethylenetriaminepentaacetic acid (DTPA) as a contrast agent for MR imaging and 18F-FDG, 11C-methionine, and 18F-NaF as molecular tracers for PET imaging. The animals were then euthanized, and complementary radiologic (micro-CT scans) and histologic analyses were performed. Results: In this preclinical study, we demonstrated that coregistered MR and PET images provide helpful information in a rat mammary–derived bone cancer model. First, MR imaging provided a high-definition anatomic resolution that made the localization of bone resorption and tumor extension detectable between days 9 and 18 after the injection of cancer cells in the medullary channel of the femur. Indeed, the calculation of mean standardized uptake value (SUVmean) and maximal SUV (SUVmax) in bone and soft-tissue regions, as defined from the gadolinium-DTPA contrast-enhanced MR images, showed 18F-NaF uptake modifications and increased 18F-FDG or 11C-methionine uptake in the bone and surrounding soft tissues. 18F-FDG and 11C-methionine were compared in terms of the magnitude of change in their uptake and variability. We observed that 11C-methionine SUVmean variations in the tumor were more important than those of 18F-FDG. We also found fewer interindividual variations using SUVmean as a quantitative parameter than SUVmax. Conclusion: This preclinical evaluation demonstrated that a PET/MR image coregistration protocol provided a powerful tool to evaluate bone tumor progression in a rat model of bone metastasis and that this protocol could be translated to improve the clinical outcome for metastatic breast cancer management. ER -