Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2019 Dec 26;20(1):619.
doi: 10.1186/s12891-019-3001-6.

Quantitative bone SPECT/CT: high specificity for identification of prostate cancer bone metastases

Affiliations

Quantitative bone SPECT/CT: high specificity for identification of prostate cancer bone metastases

Flavian Tabotta et al. BMC Musculoskelet Disord. .

Abstract

Purpose: Bone scintigraphy with 99mTc-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 99mTc-2,3-dicarboxy propane-1,1-diphosphonate (99mTc-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 SUVmax and SUVmean (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 SUVmax 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 SUVmax and SUVmean of 34.6 ± 24.6 and 20.8 ± 14.7 g/mL, respectively. In 24 spinal and pelvic osteoarthritic lesions, mean SUVmax and SUVmean were 14.2 ± 3.8 and 8.9 ± 2.2 g/mL, respectively. SUVmax and SUVmean were both significantly different between the bone metastases and osteoarthritic groups (p ≤ 0.0001). Using a SUVmax 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 99mTc-DPD uptake on bone SPECT/CT between prostate cancer bone metastases and spinal and pelvic osteoarthritic changes, with higher SUVmax and SUVmean in metastases. Using a SUVmax 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.

Keywords: 99mTc-DPD; Bone metastases; Bone scintigraphy; Prostate cancer; Prostate cancer metastases; Quantitative SPECT; SPECT/CT; SUV; Spinal osteoarthritis; xSPECT.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no conflict of interest.

Figures

Fig. 1
Fig. 1
a Osteoblastic lesion of the pelvis in a 57-year-old male patient known for prostate cancer, showing a high SUVmax of 28 g/mL and SUVmean of 17 g/mL. b Lumbar spine osteoarthritic changes of the L4-L5 facet joints in a 83-year-old male patient with hip pain, showing SUVmax of 15 and 13 g/mL and SUVmean of 9.0 and 7.8 g/mL in the left and right facet joints, respectively
Fig. 2
Fig. 2
Box-and-whisker plots of SUVmax overall (a) and depending on metastases location (b)
Fig. 3
Fig. 3
Box-and-whisker plots of SUVmax depending on presence or absence of previous systemic therapy in all bone metastases (a) and in spinal and pelvic bone metastases (b)
Fig. 4
Fig. 4
ROC curves of SUVmax and SUVmean for spinal and pelvic prostate cancer bone metastases, with AUCs of 0.947 and 0.943, respectively

References

    1. Torre LA, et al. Global cancer statistics, 2012. CA Cancer J Clin. 2015;65(2):87–108. doi: 10.3322/caac.21262. - DOI - PubMed
    1. Lin SC, et al. Endothelial-to-osteoblast conversion generates osteoblastic metastasis of prostate cancer. Dev Cell. 2017;41(5):467–480. doi: 10.1016/j.devcel.2017.05.005. - DOI - PMC - PubMed
    1. Kanishi D. 99mTc-MDP accumulation mechanisms in bone. Oral Surg Oral Med Oral Pathol. 1993;75(2):239–246. doi: 10.1016/0030-4220(93)90100-I. - DOI - PubMed
    1. Helyar V, et al. The added value of multislice SPECT/CT in patients with equivocal bony metastasis from carcinoma of the prostate. Eur J Nucl Med Mol Imaging. 2010;37(4):706–713. doi: 10.1007/s00259-009-1334-3. - DOI - PubMed
    1. Strobel K, et al. Characterization of focal bone lesions in the axial skeleton: performance of planar bone scintigraphy compared with SPECT and SPECT fused with CT. AJR Am J Roentgenol. 2007;188(5):W467–W474. doi: 10.2214/AJR.06.1215. - DOI - PubMed