Vertebral and femoral bone mineral density and bone strength in prostate cancer patients assessed in phantomless PET/CT examinations
Bone fracture risk assessed ancillary to positron emission tomography with computed tomography co-registration (PET/CT) could provide substantial clinical value to oncology patients with elevated fracture risk without introducing additional radiation dose. The purpose of our study was to investigate...
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Published in | Bone (New York, N.Y.) Vol. 101; pp. 62 - 69 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Elsevier Inc
01.08.2017
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Online Access | Get full text |
ISSN | 8756-3282 1873-2763 1873-2763 |
DOI | 10.1016/j.bone.2017.04.008 |
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Abstract | Bone fracture risk assessed ancillary to positron emission tomography with computed tomography co-registration (PET/CT) could provide substantial clinical value to oncology patients with elevated fracture risk without introducing additional radiation dose. The purpose of our study was to investigate the feasibility of obtaining valid measurements of bone mineral density (BMD) and finite element analysis-derived bone strength of the hip and spine using PET/CT examinations of prostate cancer patients by comparing against values obtained using routine multidetector-row computed tomography (MDCT) scans—as validated in previous studies—as a reference standard.
Men with prostate cancer (n=82, 71.6±8.3 years) underwent Fluorine-18 NaF PET/CT and routine MDCT within three months. Femoral neck and total hip areal BMD, vertebral trabecular BMD and femur and vertebral strength based on finite element analysis were assessed in 63 paired PET/CT and MDCT examinations using phantomless calibration and Biomechanical-CT analysis. Men with osteoporosis or fragile bone strength identified at either the hip or spine (vertebral trabecular BMD ≤80mg/cm3, femoral neck or total hip T-score ≤−2.5, vertebral strength ≤6500N and femoral strength ≤3500N, respectively) were considered to be at high risk of fracture. PET/CT- versus MDCT-based BMD and strength measurements were compared using paired t-tests, linear regression and by generating Bland-Altman plots. Agreement in fracture-risk classification was assessed in a contingency table.
All measurements from PET/CT versus MDCT were strongly correlated (R2=0.93–0.97; P<0.0001 for all). Mean differences for total hip areal BMD (0.001g/cm2, 1.1%), femoral strength (−60N, 1.3%), vertebral trabecular BMD (2mg/cm3, 2.6%) and vertebral strength (150N; 1.7%) measurements were not statistically significant (P>0.05 for all), whereas the mean difference in femoral neck areal BMD measurements was small but significant (−0.018g/cm2; −2.5%; P=0.007). The agreement between PET/CT and MDCT for fracture-risk classification was 97% (0.89 kappa for repeatability).
Ancillary analyses of BMD, bone strength, and fracture risk agreed well between PET/CT and MDCT, suggesting that PET/CT can be used opportunistically to comprehensively assess bone integrity. In subjects with high fracture risk such as cancer patients this may serve as an additional clinical tool to guide therapy planning and prevention of fractures.
•Biomechanical-CT measurements for bone mineral density (BMD) and bone strength from PET/CT are strongly correlated with those from MDCT.•Fracture-risk classification from PET/CT agrees well with that from MDCT.•Ancillary analysis of routine PET/CT examinations can provide valid assessments of BMD, bone strength, and fracture-risk classification. |
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AbstractList | Bone fracture risk assessed ancillary to positron emission tomography with computed tomography co-registration (PET/CT) could provide substantial clinical value to oncology patients with elevated fracture risk without introducing additional radiation dose. The purpose of our study was to investigate the feasibility of obtaining valid measurements of bone mineral density (BMD) and finite element analysis-derived bone strength of the hip and spine using PET/CT examinations of prostate cancer patients by comparing against values obtained using routine multidetector-row computed tomography (MDCT) scans—as validated in previous studies—as a reference standard.
Men with prostate cancer (n=82, 71.6±8.3 years) underwent Fluorine-18 NaF PET/CT and routine MDCT within three months. Femoral neck and total hip areal BMD, vertebral trabecular BMD and femur and vertebral strength based on finite element analysis were assessed in 63 paired PET/CT and MDCT examinations using phantomless calibration and Biomechanical-CT analysis. Men with osteoporosis or fragile bone strength identified at either the hip or spine (vertebral trabecular BMD ≤80mg/cm3, femoral neck or total hip T-score ≤−2.5, vertebral strength ≤6500N and femoral strength ≤3500N, respectively) were considered to be at high risk of fracture. PET/CT- versus MDCT-based BMD and strength measurements were compared using paired t-tests, linear regression and by generating Bland-Altman plots. Agreement in fracture-risk classification was assessed in a contingency table.
All measurements from PET/CT versus MDCT were strongly correlated (R2=0.93–0.97; P<0.0001 for all). Mean differences for total hip areal BMD (0.001g/cm2, 1.1%), femoral strength (−60N, 1.3%), vertebral trabecular BMD (2mg/cm3, 2.6%) and vertebral strength (150N; 1.7%) measurements were not statistically significant (P>0.05 for all), whereas the mean difference in femoral neck areal BMD measurements was small but significant (−0.018g/cm2; −2.5%; P=0.007). The agreement between PET/CT and MDCT for fracture-risk classification was 97% (0.89 kappa for repeatability).
Ancillary analyses of BMD, bone strength, and fracture risk agreed well between PET/CT and MDCT, suggesting that PET/CT can be used opportunistically to comprehensively assess bone integrity. In subjects with high fracture risk such as cancer patients this may serve as an additional clinical tool to guide therapy planning and prevention of fractures.
•Biomechanical-CT measurements for bone mineral density (BMD) and bone strength from PET/CT are strongly correlated with those from MDCT.•Fracture-risk classification from PET/CT agrees well with that from MDCT.•Ancillary analysis of routine PET/CT examinations can provide valid assessments of BMD, bone strength, and fracture-risk classification. Bone fracture risk assessed ancillary to positron emission tomography with computed tomography co-registration (PET/CT) could provide substantial clinical value to oncology patients with elevated fracture risk without introducing additional radiation dose. The purpose of our study was to investigate the feasibility of obtaining valid measurements of bone mineral density (BMD) and finite element analysis-derived bone strength of the hip and spine using PET/CT examinations of prostate cancer patients by comparing against values obtained using routine multidetector-row computed tomography (MDCT) scans-as validated in previous studies-as a reference standard.PURPOSEBone fracture risk assessed ancillary to positron emission tomography with computed tomography co-registration (PET/CT) could provide substantial clinical value to oncology patients with elevated fracture risk without introducing additional radiation dose. The purpose of our study was to investigate the feasibility of obtaining valid measurements of bone mineral density (BMD) and finite element analysis-derived bone strength of the hip and spine using PET/CT examinations of prostate cancer patients by comparing against values obtained using routine multidetector-row computed tomography (MDCT) scans-as validated in previous studies-as a reference standard.Men with prostate cancer (n=82, 71.6±8.3 years) underwent Fluorine-18 NaF PET/CT and routine MDCT within three months. Femoral neck and total hip areal BMD, vertebral trabecular BMD and femur and vertebral strength based on finite element analysis were assessed in 63 paired PET/CT and MDCT examinations using phantomless calibration and Biomechanical-CT analysis. Men with osteoporosis or fragile bone strength identified at either the hip or spine (vertebral trabecular BMD ≤80mg/cm3, femoral neck or total hip T-score ≤-2.5, vertebral strength ≤6500N and femoral strength ≤3500N, respectively) were considered to be at high risk of fracture. PET/CT- versus MDCT-based BMD and strength measurements were compared using paired t-tests, linear regression and by generating Bland-Altman plots. Agreement in fracture-risk classification was assessed in a contingency table.MATERIALS AND METHODSMen with prostate cancer (n=82, 71.6±8.3 years) underwent Fluorine-18 NaF PET/CT and routine MDCT within three months. Femoral neck and total hip areal BMD, vertebral trabecular BMD and femur and vertebral strength based on finite element analysis were assessed in 63 paired PET/CT and MDCT examinations using phantomless calibration and Biomechanical-CT analysis. Men with osteoporosis or fragile bone strength identified at either the hip or spine (vertebral trabecular BMD ≤80mg/cm3, femoral neck or total hip T-score ≤-2.5, vertebral strength ≤6500N and femoral strength ≤3500N, respectively) were considered to be at high risk of fracture. PET/CT- versus MDCT-based BMD and strength measurements were compared using paired t-tests, linear regression and by generating Bland-Altman plots. Agreement in fracture-risk classification was assessed in a contingency table.All measurements from PET/CT versus MDCT were strongly correlated (R2=0.93-0.97; P<0.0001 for all). Mean differences for total hip areal BMD (0.001g/cm2, 1.1%), femoral strength (-60N, 1.3%), vertebral trabecular BMD (2mg/cm3, 2.6%) and vertebral strength (150N; 1.7%) measurements were not statistically significant (P>0.05 for all), whereas the mean difference in femoral neck areal BMD measurements was small but significant (-0.018g/cm2; -2.5%; P=0.007). The agreement between PET/CT and MDCT for fracture-risk classification was 97% (0.89 kappa for repeatability).RESULTSAll measurements from PET/CT versus MDCT were strongly correlated (R2=0.93-0.97; P<0.0001 for all). Mean differences for total hip areal BMD (0.001g/cm2, 1.1%), femoral strength (-60N, 1.3%), vertebral trabecular BMD (2mg/cm3, 2.6%) and vertebral strength (150N; 1.7%) measurements were not statistically significant (P>0.05 for all), whereas the mean difference in femoral neck areal BMD measurements was small but significant (-0.018g/cm2; -2.5%; P=0.007). The agreement between PET/CT and MDCT for fracture-risk classification was 97% (0.89 kappa for repeatability).Ancillary analyses of BMD, bone strength, and fracture risk agreed well between PET/CT and MDCT, suggesting that PET/CT can be used opportunistically to comprehensively assess bone integrity. In subjects with high fracture risk such as cancer patients this may serve as an additional clinical tool to guide therapy planning and prevention of fractures.CONCLUSIONAncillary analyses of BMD, bone strength, and fracture risk agreed well between PET/CT and MDCT, suggesting that PET/CT can be used opportunistically to comprehensively assess bone integrity. In subjects with high fracture risk such as cancer patients this may serve as an additional clinical tool to guide therapy planning and prevention of fractures. Bone fracture risk assessed ancillary to positron emission tomography with computed tomography co-registration (PET/CT) could provide substantial clinical value to oncology patients with elevated fracture risk without introducing additional radiation dose. The purpose of our study was to investigate the feasibility of obtaining valid measurements of bone mineral density (BMD) and finite element analysis-derived bone strength of the hip and spine using PET/CT examinations of prostate cancer patients by comparing against values obtained using routine multidetector-row computed tomography (MDCT) scans-as validated in previous studies-as a reference standard. Men with prostate cancer (n=82, 71.6±8.3 years) underwent Fluorine-18 NaF PET/CT and routine MDCT within three months. Femoral neck and total hip areal BMD, vertebral trabecular BMD and femur and vertebral strength based on finite element analysis were assessed in 63 paired PET/CT and MDCT examinations using phantomless calibration and Biomechanical-CT analysis. Men with osteoporosis or fragile bone strength identified at either the hip or spine (vertebral trabecular BMD ≤80mg/cm , femoral neck or total hip T-score ≤-2.5, vertebral strength ≤6500N and femoral strength ≤3500N, respectively) were considered to be at high risk of fracture. PET/CT- versus MDCT-based BMD and strength measurements were compared using paired t-tests, linear regression and by generating Bland-Altman plots. Agreement in fracture-risk classification was assessed in a contingency table. All measurements from PET/CT versus MDCT were strongly correlated (R =0.93-0.97; P<0.0001 for all). Mean differences for total hip areal BMD (0.001g/cm , 1.1%), femoral strength (-60N, 1.3%), vertebral trabecular BMD (2mg/cm , 2.6%) and vertebral strength (150N; 1.7%) measurements were not statistically significant (P>0.05 for all), whereas the mean difference in femoral neck areal BMD measurements was small but significant (-0.018g/cm ; -2.5%; P=0.007). The agreement between PET/CT and MDCT for fracture-risk classification was 97% (0.89 kappa for repeatability). Ancillary analyses of BMD, bone strength, and fracture risk agreed well between PET/CT and MDCT, suggesting that PET/CT can be used opportunistically to comprehensively assess bone integrity. In subjects with high fracture risk such as cancer patients this may serve as an additional clinical tool to guide therapy planning and prevention of fractures. Abstract Purpose Bone fracture risk assessed ancillary to positron emission tomography with computed tomography co-registration (PET/CT) could provide substantial clinical value to oncology patients with elevated fracture risk without introducing additional radiation dose. The purpose of our study was to investigate the feasibility of obtaining valid measurements of bone mineral density (BMD) and finite element analysis-derived bone strength of the hip and spine using PET/CT examinations of prostate cancer patients by comparing against values obtained using routine multidetector-row computed tomography (MDCT) scans—as validated in previous studies—as a reference standard. Materials and methods Men with prostate cancer (n = 82, 71.6 ± 8.3 years) underwent Fluorine-18 NaF PET/CT and routine MDCT within three months. Femoral neck and total hip areal BMD, vertebral trabecular BMD and femur and vertebral strength based on finite element analysis were assessed in 63 paired PET/CT and MDCT examinations using phantomless calibration and Biomechanical-CT analysis. Men with osteoporosis or fragile bone strength identified at either the hip or spine (vertebral trabecular BMD ≤ 80 mg/cm3 , femoral neck or total hip T -score ≤− 2.5, vertebral strength ≤ 6500 N and femoral strength ≤ 3500 N, respectively) were considered to be at high risk of fracture. PET/CT- versus MDCT-based BMD and strength measurements were compared using paired t -tests, linear regression and by generating Bland-Altman plots. Agreement in fracture-risk classification was assessed in a contingency table. Results All measurements from PET/CT versus MDCT were strongly correlated (R2 = 0.93–0.97; P < 0.0001 for all). Mean differences for total hip areal BMD (0.001 g/cm2 , 1.1%), femoral strength (− 60 N, 1.3%), vertebral trabecular BMD (2 mg/cm3 , 2.6%) and vertebral strength (150 N; 1.7%) measurements were not statistically significant (P > 0.05 for all), whereas the mean difference in femoral neck areal BMD measurements was small but significant (− 0.018 g/cm2 ; − 2.5%; P = 0.007). The agreement between PET/CT and MDCT for fracture-risk classification was 97% (0.89 kappa for repeatability). Conclusion Ancillary analyses of BMD, bone strength, and fracture risk agreed well between PET/CT and MDCT, suggesting that PET/CT can be used opportunistically to comprehensively assess bone integrity. In subjects with high fracture risk such as cancer patients this may serve as an additional clinical tool to guide therapy planning and prevention of fractures. |
Author | Schwaiger, Benedikt J. Facchetti, Luca Gersing, Alexandra S. Lee, Kwang J. Keaveny, Tony M. Nardo, Lorenzo Link, Thomas M. Kopperdahl, David L. Neumann, Jan |
AuthorAffiliation | 1 Department of Radiology and Biomedical Imaging, University of California, San Francisco, CA 3 Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY 2 O.N. Diagnostics, LLC, Berkeley, CA 4 Departments of Mechanical Engineering and Bioengineering, University of California, Berkeley, CA |
AuthorAffiliation_xml | – name: 1 Department of Radiology and Biomedical Imaging, University of California, San Francisco, CA – name: 3 Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY – name: 2 O.N. Diagnostics, LLC, Berkeley, CA – name: 4 Departments of Mechanical Engineering and Bioengineering, University of California, Berkeley, CA |
Author_xml | – sequence: 1 givenname: Benedikt J. orcidid: 0000-0003-1803-1510 surname: Schwaiger fullname: Schwaiger, Benedikt J. email: bschwaiger@gmx.com organization: Department of Radiology and Biomedical Imaging, University of California, San Francisco, CA, United States – sequence: 2 givenname: David L. surname: Kopperdahl fullname: Kopperdahl, David L. email: david.kopperdahl@ondiagnostics.com organization: O.N. Diagnostics, LLC, Berkeley, CA, United States – sequence: 3 givenname: Lorenzo surname: Nardo fullname: Nardo, Lorenzo email: lornardob@gmail.com organization: Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, United States – sequence: 4 givenname: Luca surname: Facchetti fullname: Facchetti, Luca organization: Department of Radiology and Biomedical Imaging, University of California, San Francisco, CA, United States – sequence: 5 givenname: Alexandra S. orcidid: 0000-0003-1687-5541 surname: Gersing fullname: Gersing, Alexandra S. email: alexandra.gersing@ucsf.edu organization: Department of Radiology and Biomedical Imaging, University of California, San Francisco, CA, United States – sequence: 6 givenname: Jan surname: Neumann fullname: Neumann, Jan email: jan.neumann@ucsf.edu organization: Department of Radiology and Biomedical Imaging, University of California, San Francisco, CA, United States – sequence: 7 givenname: Kwang J. surname: Lee fullname: Lee, Kwang J. organization: O.N. Diagnostics, LLC, Berkeley, CA, United States – sequence: 8 givenname: Tony M. surname: Keaveny fullname: Keaveny, Tony M. email: tonykeaveny@berkeley.edu organization: Departments of Mechanical Engineering and Bioengineering, University of California, Berkeley, CA, United States – sequence: 9 givenname: Thomas M. surname: Link fullname: Link, Thomas M. email: thomas.link@ucsf.edu organization: Department of Radiology and Biomedical Imaging, University of California, San Francisco, CA, United States |
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Keywords | Biomechanical-CT Bone mineral density Finite element analysis MDCT Bone strength Prostate cancer 18F-NaF PET/CT Cancer-induced bone disease |
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Snippet | Bone fracture risk assessed ancillary to positron emission tomography with computed tomography co-registration (PET/CT) could provide substantial clinical... Abstract Purpose Bone fracture risk assessed ancillary to positron emission tomography with computed tomography co-registration (PET/CT) could provide... |
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SubjectTerms | 18F-NaF PET/CT Absorptiometry, Photon Aged Aged, 80 and over Biomechanical Phenomena Biomechanical-CT Bone Density - physiology Bone mineral density Bone strength Cancer-induced bone disease Femur Neck - pathology Femur Neck - physiopathology Finite Element Analysis Humans Male MDCT Middle Aged Orthopedics Osteoporosis - pathology Osteoporosis - physiopathology Positron Emission Tomography Computed Tomography - methods Prostate cancer Prostatic Neoplasms - pathology Prostatic Neoplasms - physiopathology |
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Title | Vertebral and femoral bone mineral density and bone strength in prostate cancer patients assessed in phantomless PET/CT examinations |
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