Abstract
Purpose
To compare the diagnostic accuracy of whole-body PET/CT and integrated PET/MR in relation to the total scan time durations.
Methods
One hundred and twenty-three (123) patients (40 males and 83 females; mean age 59.6 years; range 20–83 years) with confirmed primary cancer and clinical suspicion of metastatic disease underwent whole-body 18F-FDG-PET/CT and 18F-FDG-PET/MR. Data acquisition was done after intravenous administration of 110–301 MBq radioactivity of 18F-FDG, and PET/MR data were acquired after the PET/CT data acquisition. The mean uptake times for PET/CT and PET/MR acquisition were 68.0 ± 8.0 and 98.0 ± 14 min, respectively. Total scan time was 20.0 and 25.0 min for whole-body PET/CT and PET/MR imaging.
Results
The reconstructed PET/CT and PET/MR data detected 333/355 (93.8 %) common lesions in 111/123 (90.2 %) patients. PET/CT and PET/MR alone detected 348/355 and 340/355 lesions, respectively. No significant (p = 0.08) difference was observed for the overall detection efficiency between the two techniques. On the other hand, a significant difference was observed between the two techniques for the detection of lung (p = 0.003) and cerebrospinal (p = 0.007) lesions. The 15 lesions identified by PET/CT only included 8 lung, 3 lymph nodes, 2 bone, and 1 each of peritoneal and adrenal gland lesions. On the other hand, 7 (6 brain metastatic lesions and 1 bone lesion) were identified by PET/MR only.
Conclusion
Integrated PET/MR is a feasible whole-body imaging modality and may score better than PET/CT for the detection of brain metastases. To further prove diagnostic utility, this technique requires further clinical validation.
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Acknowledgments
We are grateful for the assistance of Seiichi Takenoshita, doctors of the Department of Organ Regulatory Surgery and Radiology, and the staff of Advanced Clinical Research Center for their support in performing this study.
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Ishii, S., Shimao, D., Hara, T. et al. Comparison of integrated whole-body PET/MR and PET/CT: Is PET/MR alternative to PET/CT in routine clinical oncology?. Ann Nucl Med 30, 225–233 (2016). https://doi.org/10.1007/s12149-015-1050-y
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DOI: https://doi.org/10.1007/s12149-015-1050-y