Characterization of Bone Lesions in Myeloma Before and During Anticancer Therapy Using 18F-FDG-PET/CT and 18F-NaF-PET/CT

被引:3
作者
Nakuz, Thomas Selim [1 ]
Millinger, Filipe Portela [1 ]
El-Rabadi, Karem [2 ]
Weber, Michael [2 ]
Pichler, Verena [1 ]
Wadsak, Wolfgang [1 ,3 ]
Mitterhauser, Markus [1 ,4 ]
Haug, Alexander [1 ]
Hacker, Marcus [1 ]
Karanikas, Georgios [1 ]
Pietschmann, Peter [5 ]
Agis, Hermine [6 ]
机构
[1] Med Univ Vienna, Div Nucl Med, Dept Biomed Imaging & Image Guided Therapy, Vienna, Austria
[2] Med Univ Vienna, Div Radiol, Vienna, Austria
[3] Ctr Biomarker Res Med, Graz, Austria
[4] Ludwig Boltzmann Inst Appl Diagnost, Vienna, Austria
[5] Med Univ Vienna, Ctr Pathophysiol Infectiol & Immunol, Dept Pathophysiol & Allergy Res, Vienna, Austria
[6] Med Univ Vienna, Dept Internal Med 1, Div Oncol, Vienna, Austria
关键词
PET; multiple myeloma; F-18-FDG; F-18-sodium fluoride; positron-emission tomography; PET/CT; POSITRON-EMISSION-TOMOGRAPHY; MULTIPLE-MYELOMA; FDG PET/CT; F-18-FLUORIDE; STATEMENT; DIAGNOSIS; CRITERIA; DISEASE;
D O I
10.21873/anticanres.13304
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The objective of this study was to characterize tumor activity and mineralization status in newly-detected multiple myeloma (MM) bone lesions using 2-F-18-fluoro-2-deoxy-D-glucose (F-18-FDG)-PET/CT and F-18-sodium fluoride (F-18-NaF)-PET/CT before and after antitumor treatment. Materials and Methods: In this retrospective study, seven patients with histologically-verified MM were included (four women, three men; median age=57 years, standard deviation=11.23 years). PET/CT was performed with F-18-FDG and with F-18-NaF, both at baseline and after treatment. All patients had positive scans. Volumes of interest (VOIs) were drawn over all F-18-FDG-PET/CT-positive bone lesions, as well as the corresponding regions in F-18-NaF-PET/CT. For characterization of bone lesions, semi-quantitative standard uptake value (SUV) parameters were measured. Results: F-18-FDG-PET/CT in the seven patients detected 39 metabolically active lesions that were correlated with the corresponding sites in F-18-fluoride-PET/CT. Overall, the lesions showed a response to therapy, with a significant decrease in SUVmax on PET/CT using F-18-FDG (p< 0.001) and with F-18-NaF (p< 0.001). In four patients with a second follow-up scan (at a median of 17 months after baseline scan), there was no significant change in lesion uptake. Conclusion: Based on our data, antitumor therapy in MM reduces not only tumor activity, but also the mineralization status of bone lesions. A second follow-up scan in a subset of the cohort yielded no change in mineralization status.
引用
收藏
页码:1943 / 1952
页数:10
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