68Ga-PSMA-11 PET/CT derived quantitative volumetric tumor parameters for classification and evaluation of therapeutic response of bone metastases in prostate cancer patients

Background To evaluate the role of 68 Gallium prostate-specific membrane antigen-positron emission tomography/computed tomography ( 68 Ga-PSMA-11 PET/CT) derived quantitative volumetric tumor parameters in comparison with fully diagnostic conventional CT and serum-PSA levels for classification and e...

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Veröffentlicht in:Annals of nuclear medicine 2019-10, Vol.33 (10), p.766-775
Hauptverfasser: Schmidkonz, Christian, Cordes, Michael, Goetz, Theresa Ida, Prante, Olaf, Kuwert, Torsten, Ritt, Philipp, Uder, Michael, Wullich, Bernd, Goebell, Peter, Bäuerle, Tobias
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container_issue 10
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container_title Annals of nuclear medicine
container_volume 33
creator Schmidkonz, Christian
Cordes, Michael
Goetz, Theresa Ida
Prante, Olaf
Kuwert, Torsten
Ritt, Philipp
Uder, Michael
Wullich, Bernd
Goebell, Peter
Bäuerle, Tobias
description Background To evaluate the role of 68 Gallium prostate-specific membrane antigen-positron emission tomography/computed tomography ( 68 Ga-PSMA-11 PET/CT) derived quantitative volumetric tumor parameters in comparison with fully diagnostic conventional CT and serum-PSA levels for classification and evaluation of therapeutic response of bone metastases in patients with metastasized prostate cancer (PC). Methods A total of 177 men with biochemical recurrence of prostate cancer suffering from bone metastases underwent PET/CT with [ 68 Ga] Ga-PSMA-HBED-CC ( 68 Ga-PSMA-11). To calculate 68 Ga-PSMA-11 PET quantitative volumetric tumor parameters including whole-body total-lesion PSMA (TL-PSMA), whole-body PSMA-tumor volume (PSMA-TV), as well as the established maximum standard uptake values (SUVmax) and mean standard uptake values (SUVmean), all 443 68 Ga-PSMA-11-positive bone lesions in the field of view were assessed quantitatively. Quantitative volumetric tumor parameters were correlated with CT-derived volume and bone density measurements of metastatic bone lesions, serum prostate-specific antigen (PSA) levels, and Gleason Scores. In the 20 patients suffering from bone metastases who underwent 68 Ga-PSMA-11 PET/CT before and after therapy, CT-derived volume and bone density measurements of metastatic lesions were compared to biochemical response determined by serum-PSA levels. Results In 177 patients, a total of 443 68 Ga-PSMA-11 PET-positive bone lesions were detected. Of these, 50 lesions (11%) were only detectable on PET but not on conventional CT. PET-positive/CT-negative bone metastases demonstrated a significantly lower PSMA uptake compared to PET-positive/CT-positive bone lesions ( p   0.05) before and after therapy, while a highly significant correlation was observed for changes of PSMA-TV, TL-PSMA, and serum-PSA levels ( p  
doi_str_mv 10.1007/s12149-019-01387-0
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Methods A total of 177 men with biochemical recurrence of prostate cancer suffering from bone metastases underwent PET/CT with [ 68 Ga] Ga-PSMA-HBED-CC ( 68 Ga-PSMA-11). To calculate 68 Ga-PSMA-11 PET quantitative volumetric tumor parameters including whole-body total-lesion PSMA (TL-PSMA), whole-body PSMA-tumor volume (PSMA-TV), as well as the established maximum standard uptake values (SUVmax) and mean standard uptake values (SUVmean), all 443 68 Ga-PSMA-11-positive bone lesions in the field of view were assessed quantitatively. Quantitative volumetric tumor parameters were correlated with CT-derived volume and bone density measurements of metastatic bone lesions, serum prostate-specific antigen (PSA) levels, and Gleason Scores. In the 20 patients suffering from bone metastases who underwent 68 Ga-PSMA-11 PET/CT before and after therapy, CT-derived volume and bone density measurements of metastatic lesions were compared to biochemical response determined by serum-PSA levels. Results In 177 patients, a total of 443 68 Ga-PSMA-11 PET-positive bone lesions were detected. Of these, 50 lesions (11%) were only detectable on PET but not on conventional CT. PET-positive/CT-negative bone metastases demonstrated a significantly lower PSMA uptake compared to PET-positive/CT-positive bone lesions ( p  &lt; 0.05). SUVmax, SUVmean, PSMA-TV, and TL-PSMA of bone metastases were significantly higher ( p  &lt; 0.05) in patients with Gleason Scores &gt; 7 compared to those with Gleason Scores ≤ 7. In the linear regression analysis, an association was determined between SUVmean, Gleason Scores, lesion classification, and serum-PSA levels but not for CT-derived bone density measurements. No significant correlation could be found between changes of bone density and CT-derived volume measurements of metastatic bone lesions and changes of serum-PSA levels ( p  &gt; 0.05) before and after therapy, while a highly significant correlation was observed for changes of PSMA-TV, TL-PSMA, and serum-PSA levels ( p  &lt; 0.001). Conclusion Our results suggest that 68 Ga-PSMA-11 PET/CT might be a valuable tool for the detection and follow-up of bone metastases in patients with metastasized prostate cancer. 68 Ga-PSMA-11 PET-derived quantitative volumetric parameters demonstrated a highly significant correlation with changes of serum-PSA levels during the course of therapy. No such correlation could be determined for bone density measurements of metastatic bone lesions. Compared to the fully diagnostic CT scan, a significantly higher proportion of bone metastases was detected on 68 Ga-PSMA-11 PET.</description><identifier>ISSN: 0914-7187</identifier><identifier>EISSN: 1864-6433</identifier><identifier>DOI: 10.1007/s12149-019-01387-0</identifier><identifier>PMID: 31338731</identifier><language>eng</language><publisher>Singapore: Springer Singapore</publisher><subject>Aged ; Aged, 80 and over ; Antigens ; Bone cancer ; Bone density ; Bone lesions ; Bone Neoplasms - diagnostic imaging ; Bone Neoplasms - secondary ; Bone Neoplasms - therapy ; Classification ; Computed tomography ; Correlation analysis ; Diagnostic systems ; Edetic Acid - analogs &amp; derivatives ; Emission analysis ; Evaluation ; Field of view ; Humans ; Imaging ; Lesions ; Male ; Medicine ; Medicine &amp; Public Health ; Metastases ; Metastasis ; Middle Aged ; Neoplasm Grading ; Nuclear Medicine ; Oligopeptides ; Original Article ; Parameters ; Personal computers ; Positron emission ; Positron emission tomography ; Positron Emission Tomography Computed Tomography ; Prostate cancer ; Prostate-specific antigen ; Prostatic Neoplasms - metabolism ; Prostatic Neoplasms - pathology ; Radiology ; Recurrence ; Regression analysis ; Therapy ; Time Factors ; Tomography ; Treatment Outcome ; Tumors</subject><ispartof>Annals of nuclear medicine, 2019-10, Vol.33 (10), p.766-775</ispartof><rights>The Japanese Society of Nuclear Medicine 2019</rights><rights>Copyright Springer Nature B.V. 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c399t-36299b37958a50ce7a54cb47d86fc5971b54c8ec66263f4426b54854d922381a3</citedby><cites>FETCH-LOGICAL-c399t-36299b37958a50ce7a54cb47d86fc5971b54c8ec66263f4426b54854d922381a3</cites><orcidid>0000-0002-1988-0058</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12149-019-01387-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12149-019-01387-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31338731$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schmidkonz, Christian</creatorcontrib><creatorcontrib>Cordes, Michael</creatorcontrib><creatorcontrib>Goetz, Theresa Ida</creatorcontrib><creatorcontrib>Prante, Olaf</creatorcontrib><creatorcontrib>Kuwert, Torsten</creatorcontrib><creatorcontrib>Ritt, Philipp</creatorcontrib><creatorcontrib>Uder, Michael</creatorcontrib><creatorcontrib>Wullich, Bernd</creatorcontrib><creatorcontrib>Goebell, Peter</creatorcontrib><creatorcontrib>Bäuerle, Tobias</creatorcontrib><title>68Ga-PSMA-11 PET/CT derived quantitative volumetric tumor parameters for classification and evaluation of therapeutic response of bone metastases in prostate cancer patients</title><title>Annals of nuclear medicine</title><addtitle>Ann Nucl Med</addtitle><addtitle>Ann Nucl Med</addtitle><description>Background To evaluate the role of 68 Gallium prostate-specific membrane antigen-positron emission tomography/computed tomography ( 68 Ga-PSMA-11 PET/CT) derived quantitative volumetric tumor parameters in comparison with fully diagnostic conventional CT and serum-PSA levels for classification and evaluation of therapeutic response of bone metastases in patients with metastasized prostate cancer (PC). Methods A total of 177 men with biochemical recurrence of prostate cancer suffering from bone metastases underwent PET/CT with [ 68 Ga] Ga-PSMA-HBED-CC ( 68 Ga-PSMA-11). To calculate 68 Ga-PSMA-11 PET quantitative volumetric tumor parameters including whole-body total-lesion PSMA (TL-PSMA), whole-body PSMA-tumor volume (PSMA-TV), as well as the established maximum standard uptake values (SUVmax) and mean standard uptake values (SUVmean), all 443 68 Ga-PSMA-11-positive bone lesions in the field of view were assessed quantitatively. Quantitative volumetric tumor parameters were correlated with CT-derived volume and bone density measurements of metastatic bone lesions, serum prostate-specific antigen (PSA) levels, and Gleason Scores. In the 20 patients suffering from bone metastases who underwent 68 Ga-PSMA-11 PET/CT before and after therapy, CT-derived volume and bone density measurements of metastatic lesions were compared to biochemical response determined by serum-PSA levels. Results In 177 patients, a total of 443 68 Ga-PSMA-11 PET-positive bone lesions were detected. Of these, 50 lesions (11%) were only detectable on PET but not on conventional CT. PET-positive/CT-negative bone metastases demonstrated a significantly lower PSMA uptake compared to PET-positive/CT-positive bone lesions ( p  &lt; 0.05). SUVmax, SUVmean, PSMA-TV, and TL-PSMA of bone metastases were significantly higher ( p  &lt; 0.05) in patients with Gleason Scores &gt; 7 compared to those with Gleason Scores ≤ 7. In the linear regression analysis, an association was determined between SUVmean, Gleason Scores, lesion classification, and serum-PSA levels but not for CT-derived bone density measurements. No significant correlation could be found between changes of bone density and CT-derived volume measurements of metastatic bone lesions and changes of serum-PSA levels ( p  &gt; 0.05) before and after therapy, while a highly significant correlation was observed for changes of PSMA-TV, TL-PSMA, and serum-PSA levels ( p  &lt; 0.001). Conclusion Our results suggest that 68 Ga-PSMA-11 PET/CT might be a valuable tool for the detection and follow-up of bone metastases in patients with metastasized prostate cancer. 68 Ga-PSMA-11 PET-derived quantitative volumetric parameters demonstrated a highly significant correlation with changes of serum-PSA levels during the course of therapy. No such correlation could be determined for bone density measurements of metastatic bone lesions. Compared to the fully diagnostic CT scan, a significantly higher proportion of bone metastases was detected on 68 Ga-PSMA-11 PET.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antigens</subject><subject>Bone cancer</subject><subject>Bone density</subject><subject>Bone lesions</subject><subject>Bone Neoplasms - diagnostic imaging</subject><subject>Bone Neoplasms - secondary</subject><subject>Bone Neoplasms - therapy</subject><subject>Classification</subject><subject>Computed tomography</subject><subject>Correlation analysis</subject><subject>Diagnostic systems</subject><subject>Edetic Acid - analogs &amp; derivatives</subject><subject>Emission analysis</subject><subject>Evaluation</subject><subject>Field of view</subject><subject>Humans</subject><subject>Imaging</subject><subject>Lesions</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Neoplasm Grading</subject><subject>Nuclear Medicine</subject><subject>Oligopeptides</subject><subject>Original Article</subject><subject>Parameters</subject><subject>Personal computers</subject><subject>Positron emission</subject><subject>Positron emission tomography</subject><subject>Positron Emission Tomography Computed Tomography</subject><subject>Prostate cancer</subject><subject>Prostate-specific antigen</subject><subject>Prostatic Neoplasms - metabolism</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Radiology</subject><subject>Recurrence</subject><subject>Regression analysis</subject><subject>Therapy</subject><subject>Time Factors</subject><subject>Tomography</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><issn>0914-7187</issn><issn>1864-6433</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kd2K1TAUhYMoznH0BbyQgDfexMlf2-RyOIyjMOKAx-uSprvaoU07-TngQ_mO7mNHBS-EhLB2vr12wiLkpeBvBefNRRJSaMu4OG1lGsYfkZ0wtWa1Vuox2XErNGuEac7Is5TuOJemMvIpOVNCIa_EjvyozbVjt58_XjIh6O3V4WJ_oD3E8Qg9vS8u5DG7jIoel6nMkOPoaS7zEunqosMCxEQHlH5yKY3D6BFfAnWhp3B0U9nkMtD8DaJboWR0iJDWJSQ41bslAEUjl3BBomOga1xQZKDeBQ-nUXmEkNNz8mRwU4IXD-c5-fLu6rB_z24-XX_YX94wr6zNTNXS2k41tjKu4h4aV2nf6aY39eAr24gOtQFf17JWg9ayxoKpdG-lVEY4dU7ebL74kPsCKbfzmDxMkwuwlNRK7FNSyUoh-vof9G4pMeDrkLJWN5YrjZTcKI8_SxGGdo3j7OL3VvD2FGa7hdlimO2vMFuOTa8erEs3Q_-n5Xd6CKgNSHgVvkL8O_s_tj8Bk52rsQ</recordid><startdate>20191001</startdate><enddate>20191001</enddate><creator>Schmidkonz, Christian</creator><creator>Cordes, Michael</creator><creator>Goetz, Theresa Ida</creator><creator>Prante, Olaf</creator><creator>Kuwert, Torsten</creator><creator>Ritt, Philipp</creator><creator>Uder, Michael</creator><creator>Wullich, Bernd</creator><creator>Goebell, Peter</creator><creator>Bäuerle, Tobias</creator><general>Springer Singapore</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1988-0058</orcidid></search><sort><creationdate>20191001</creationdate><title>68Ga-PSMA-11 PET/CT derived quantitative volumetric tumor parameters for classification and evaluation of therapeutic response of bone metastases in prostate cancer patients</title><author>Schmidkonz, Christian ; Cordes, Michael ; Goetz, Theresa Ida ; Prante, Olaf ; Kuwert, Torsten ; Ritt, Philipp ; Uder, Michael ; Wullich, Bernd ; Goebell, Peter ; Bäuerle, Tobias</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c399t-36299b37958a50ce7a54cb47d86fc5971b54c8ec66263f4426b54854d922381a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antigens</topic><topic>Bone cancer</topic><topic>Bone density</topic><topic>Bone lesions</topic><topic>Bone Neoplasms - diagnostic imaging</topic><topic>Bone Neoplasms - secondary</topic><topic>Bone Neoplasms - therapy</topic><topic>Classification</topic><topic>Computed tomography</topic><topic>Correlation analysis</topic><topic>Diagnostic systems</topic><topic>Edetic Acid - analogs &amp; derivatives</topic><topic>Emission analysis</topic><topic>Evaluation</topic><topic>Field of view</topic><topic>Humans</topic><topic>Imaging</topic><topic>Lesions</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Neoplasm Grading</topic><topic>Nuclear Medicine</topic><topic>Oligopeptides</topic><topic>Original Article</topic><topic>Parameters</topic><topic>Personal computers</topic><topic>Positron emission</topic><topic>Positron emission tomography</topic><topic>Positron Emission Tomography Computed Tomography</topic><topic>Prostate cancer</topic><topic>Prostate-specific antigen</topic><topic>Prostatic Neoplasms - metabolism</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Radiology</topic><topic>Recurrence</topic><topic>Regression analysis</topic><topic>Therapy</topic><topic>Time Factors</topic><topic>Tomography</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schmidkonz, Christian</creatorcontrib><creatorcontrib>Cordes, Michael</creatorcontrib><creatorcontrib>Goetz, Theresa Ida</creatorcontrib><creatorcontrib>Prante, Olaf</creatorcontrib><creatorcontrib>Kuwert, Torsten</creatorcontrib><creatorcontrib>Ritt, Philipp</creatorcontrib><creatorcontrib>Uder, Michael</creatorcontrib><creatorcontrib>Wullich, Bernd</creatorcontrib><creatorcontrib>Goebell, Peter</creatorcontrib><creatorcontrib>Bäuerle, Tobias</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of nuclear medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schmidkonz, Christian</au><au>Cordes, Michael</au><au>Goetz, Theresa Ida</au><au>Prante, Olaf</au><au>Kuwert, Torsten</au><au>Ritt, Philipp</au><au>Uder, Michael</au><au>Wullich, Bernd</au><au>Goebell, Peter</au><au>Bäuerle, Tobias</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>68Ga-PSMA-11 PET/CT derived quantitative volumetric tumor parameters for classification and evaluation of therapeutic response of bone metastases in prostate cancer patients</atitle><jtitle>Annals of nuclear medicine</jtitle><stitle>Ann Nucl Med</stitle><addtitle>Ann Nucl Med</addtitle><date>2019-10-01</date><risdate>2019</risdate><volume>33</volume><issue>10</issue><spage>766</spage><epage>775</epage><pages>766-775</pages><issn>0914-7187</issn><eissn>1864-6433</eissn><abstract>Background To evaluate the role of 68 Gallium prostate-specific membrane antigen-positron emission tomography/computed tomography ( 68 Ga-PSMA-11 PET/CT) derived quantitative volumetric tumor parameters in comparison with fully diagnostic conventional CT and serum-PSA levels for classification and evaluation of therapeutic response of bone metastases in patients with metastasized prostate cancer (PC). Methods A total of 177 men with biochemical recurrence of prostate cancer suffering from bone metastases underwent PET/CT with [ 68 Ga] Ga-PSMA-HBED-CC ( 68 Ga-PSMA-11). To calculate 68 Ga-PSMA-11 PET quantitative volumetric tumor parameters including whole-body total-lesion PSMA (TL-PSMA), whole-body PSMA-tumor volume (PSMA-TV), as well as the established maximum standard uptake values (SUVmax) and mean standard uptake values (SUVmean), all 443 68 Ga-PSMA-11-positive bone lesions in the field of view were assessed quantitatively. Quantitative volumetric tumor parameters were correlated with CT-derived volume and bone density measurements of metastatic bone lesions, serum prostate-specific antigen (PSA) levels, and Gleason Scores. In the 20 patients suffering from bone metastases who underwent 68 Ga-PSMA-11 PET/CT before and after therapy, CT-derived volume and bone density measurements of metastatic lesions were compared to biochemical response determined by serum-PSA levels. Results In 177 patients, a total of 443 68 Ga-PSMA-11 PET-positive bone lesions were detected. Of these, 50 lesions (11%) were only detectable on PET but not on conventional CT. PET-positive/CT-negative bone metastases demonstrated a significantly lower PSMA uptake compared to PET-positive/CT-positive bone lesions ( p  &lt; 0.05). SUVmax, SUVmean, PSMA-TV, and TL-PSMA of bone metastases were significantly higher ( p  &lt; 0.05) in patients with Gleason Scores &gt; 7 compared to those with Gleason Scores ≤ 7. In the linear regression analysis, an association was determined between SUVmean, Gleason Scores, lesion classification, and serum-PSA levels but not for CT-derived bone density measurements. No significant correlation could be found between changes of bone density and CT-derived volume measurements of metastatic bone lesions and changes of serum-PSA levels ( p  &gt; 0.05) before and after therapy, while a highly significant correlation was observed for changes of PSMA-TV, TL-PSMA, and serum-PSA levels ( p  &lt; 0.001). Conclusion Our results suggest that 68 Ga-PSMA-11 PET/CT might be a valuable tool for the detection and follow-up of bone metastases in patients with metastasized prostate cancer. 68 Ga-PSMA-11 PET-derived quantitative volumetric parameters demonstrated a highly significant correlation with changes of serum-PSA levels during the course of therapy. No such correlation could be determined for bone density measurements of metastatic bone lesions. Compared to the fully diagnostic CT scan, a significantly higher proportion of bone metastases was detected on 68 Ga-PSMA-11 PET.</abstract><cop>Singapore</cop><pub>Springer Singapore</pub><pmid>31338731</pmid><doi>10.1007/s12149-019-01387-0</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-1988-0058</orcidid></addata></record>
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subjects Aged
Aged, 80 and over
Antigens
Bone cancer
Bone density
Bone lesions
Bone Neoplasms - diagnostic imaging
Bone Neoplasms - secondary
Bone Neoplasms - therapy
Classification
Computed tomography
Correlation analysis
Diagnostic systems
Edetic Acid - analogs & derivatives
Emission analysis
Evaluation
Field of view
Humans
Imaging
Lesions
Male
Medicine
Medicine & Public Health
Metastases
Metastasis
Middle Aged
Neoplasm Grading
Nuclear Medicine
Oligopeptides
Original Article
Parameters
Personal computers
Positron emission
Positron emission tomography
Positron Emission Tomography Computed Tomography
Prostate cancer
Prostate-specific antigen
Prostatic Neoplasms - metabolism
Prostatic Neoplasms - pathology
Radiology
Recurrence
Regression analysis
Therapy
Time Factors
Tomography
Treatment Outcome
Tumors
title 68Ga-PSMA-11 PET/CT derived quantitative volumetric tumor parameters for classification and evaluation of therapeutic response of bone metastases in prostate cancer patients
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