BMC Musculoskeletal Disorders · 2019 · 74 citations · 16 references
MedicineNuclear MedicineRadiologyBone ScintigraphyDiagnostic ImagingDiagnostic RadiologyBone MetastasisBone Metastasis ImagingBone Tumor ImagingGenitourinary Oncology ImagingMetastatic Bone DiseaseProstate Cancer ImagingMetastatic Bone Disease DetectionMetastatic Bone Lesion ImagingOsteoarthritic ChangeProstate Cancer Bone Metastasis ImagingQuantitative Bone ImagingQuantitative Bone ScintigraphyRadionuclide Bone ScintigraphyScintigraphic Uptake Interpretation
Abstract Purpose Bone scintigraphy with 99m Tc-labeled diphosphonates can identify prostate cancer bone metastases with high sensitivity, but relatively low specificity, because benign conditions such as osteoarthritis can also trigger osteoblastic reactions. We aimed to investigate the diagnostic performance of 99m Tc-2,3-dicarboxy propane-1,1-diphosphonate ( 99m Tc-DPD) uptake quantification by single-photon emission computed tomography coupled with computed tomography (SPECT/CT) for distinguishing prostate cancer bone metastases from spinal and pelvic osteoarthritic lesions. Methods We retrospectively assessed 26 bone scans from 26 patients with known prostate cancer bone metastases and 13 control patients with benign spinal and pelvic osteoarthritic changes without known neoplastic disease. Quantitative SPECT/CT (xSPECT, Siemens Symbia Intevo, Erlangen, Germany) was performed and standardized uptake values (SUVs) were quantified with measurements of SUV max and SUV mean (g/mL) in all bone metastases for the prostate cancer group and in spinal and pelvic osteoarthritic changes for the control group. We used receiver operating characteristics (ROC) curves to determine the optimum SUV max cutoff value to distinguish between bone metastases and benign spinal and pelvic lesions. Results In total, 264 prostate cancer bone metastases were analyzed, showing a mean SUV max and SUV mean of 34.6 ± 24.6 and 20.8 ± 14.7 g/mL, respectively. In 24 spinal and pelvic osteoarthritic lesions, mean SUV max and SUV mean were 14.2 ± 3.8 and 8.9 ± 2.2 g/mL, respectively. SUV max and SUV mean were both significantly different between the bone metastases and osteoarthritic groups ( p ≤ 0.0001). Using a SUV max cutoff of 19.5 g/mL for prostate cancer bone metastases in the spine and pelvis, sensitivity, specificity, positive and negative predictive values were 87, 92, 99 and 49%, respectively. Conclusion This study showed significant differences in quantitative 99m Tc-DPD uptake on bone SPECT/CT between prostate cancer bone metastases and spinal and pelvic osteoarthritic changes, with higher SUV max and SUV mean in metastases. Using a SUV max cutoff of 19.5 g/mL, high specificity and positive predictive value for metastases identification in the spine and pelvis were found, thus increasing accuracy of bone scintigraphy.
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