NaF PET/CT for Response Assessment of Prostate Cancer Bone Metastases Treated with Single Fraction Stereotactic Ablative Body Radiotherapy
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Introduction: In prostate cancer patients, imaging of bone metastases is enhanced through the use of sodium fluoride positron emission tomography (F-NaF PET/CT). This imaging technique shows areas of enhanced osteoblastic activity and blood flow. In this work, F-NaF PET/CT was investigated for response assessment to single fraction stereotactic ablative body radiotherapy (SABR) to bone metastases in prostate cancer patients.
Methods: Patients with bone metastases in a prospective trial treated with single fraction SABR received a F-NaF PET/CT scan prior to and 6 months post-SABR. The SUV in the tumour was determined and the difference between before and after SABR determined. The change in uptake in the non-tumour bone was also measured as a function of the received SABR dose.
Results: Reduction in SUV was observed in 29 of 33 lesions 6 months after SABR (mean absolute decrease in SUV 17.7, 95% CI 25.8 to - 9.4, p = 0.0001). Of the three lesions with increased SUV post-SABR, two were from the same patient and located in the vertebral column. Both were determined to be local progression in addition to one fracture. The third lesion (in a rib) was shown to be controlled locally but suffered from a fracture at 24 months. Progression adjacent to the treated volume was observed in two patients. The non-tumour bone irradiated showed increased loss in uptake with increasing dose, with a median loss in uptake of 23.3% for bone receiving 24 Gy.
Conclusion: F-NaF PET/CT for response assessment of bone metastases to single fraction SABR indicates high rates of reduction of osteoblastic activity in the tumour and non-tumour bone receiving high doses. The occurrence of marginal recurrence indicates use of larger clinical target volumes may be warranted in treatment of bone metastases.
Trial Registration: POPSTAR, 'Pilot Study of patients with Oligometastases from Prostate cancer treated with STereotactic Ablative Radiotherapy', Universal Trial Number U1111-1140-7563 , Registered 17th April 2013.
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