Cargando…

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

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 performa...

Descripción completa

Detalles Bibliográficos
Autores principales: Tabotta, Flavian, Jreige, Mario, Schaefer, Niklaus, Becce, Fabio, Prior, John O., Nicod Lalonde, Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933900/
https://www.ncbi.nlm.nih.gov/pubmed/31878904
http://dx.doi.org/10.1186/s12891-019-3001-6
_version_ 1783483299562258432
author Tabotta, Flavian
Jreige, Mario
Schaefer, Niklaus
Becce, Fabio
Prior, John O.
Nicod Lalonde, Marie
author_facet Tabotta, Flavian
Jreige, Mario
Schaefer, Niklaus
Becce, Fabio
Prior, John O.
Nicod Lalonde, Marie
author_sort Tabotta, Flavian
collection PubMed
description 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.
format Online
Article
Text
id pubmed-6933900
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-69339002019-12-30 Quantitative bone SPECT/CT: high specificity for identification of prostate cancer bone metastases Tabotta, Flavian Jreige, Mario Schaefer, Niklaus Becce, Fabio Prior, John O. Nicod Lalonde, Marie BMC Musculoskelet Disord Research Article 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. BioMed Central 2019-12-26 /pmc/articles/PMC6933900/ /pubmed/31878904 http://dx.doi.org/10.1186/s12891-019-3001-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Tabotta, Flavian
Jreige, Mario
Schaefer, Niklaus
Becce, Fabio
Prior, John O.
Nicod Lalonde, Marie
Quantitative bone SPECT/CT: high specificity for identification of prostate cancer bone metastases
title Quantitative bone SPECT/CT: high specificity for identification of prostate cancer bone metastases
title_full Quantitative bone SPECT/CT: high specificity for identification of prostate cancer bone metastases
title_fullStr Quantitative bone SPECT/CT: high specificity for identification of prostate cancer bone metastases
title_full_unstemmed Quantitative bone SPECT/CT: high specificity for identification of prostate cancer bone metastases
title_short Quantitative bone SPECT/CT: high specificity for identification of prostate cancer bone metastases
title_sort quantitative bone spect/ct: high specificity for identification of prostate cancer bone metastases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933900/
https://www.ncbi.nlm.nih.gov/pubmed/31878904
http://dx.doi.org/10.1186/s12891-019-3001-6
work_keys_str_mv AT tabottaflavian quantitativebonespectcthighspecificityforidentificationofprostatecancerbonemetastases
AT jreigemario quantitativebonespectcthighspecificityforidentificationofprostatecancerbonemetastases
AT schaeferniklaus quantitativebonespectcthighspecificityforidentificationofprostatecancerbonemetastases
AT beccefabio quantitativebonespectcthighspecificityforidentificationofprostatecancerbonemetastases
AT priorjohno quantitativebonespectcthighspecificityforidentificationofprostatecancerbonemetastases
AT nicodlalondemarie quantitativebonespectcthighspecificityforidentificationofprostatecancerbonemetastases