Expert System for Bone Scan Interpretation Improves Progression Assessment in Bone Metastatic Prostate Cancer

Introduction The bone scan index (BSI) was introduced as a quantitative tool for tumor involvement in bone of patients with metastatic prostate cancer (mPCa). The computer-aided diagnosis device for BSI analysis EXINIbone BSI seems to represent technical progress for the quantitative assessment of b...

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Veröffentlicht in:Advances in therapy 2017-04, Vol.34 (4), p.986-994
Hauptverfasser: Haupt, Fabian, Berding, Georg, Namazian, Ali, Wilke, Florian, Böker, Alena, Merseburger, Axel, Geworski, Lilli, Kuczyk, Markus Antonius, Bengel, Frank Michael, Peters, Inga
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container_start_page 986
container_title Advances in therapy
container_volume 34
creator Haupt, Fabian
Berding, Georg
Namazian, Ali
Wilke, Florian
Böker, Alena
Merseburger, Axel
Geworski, Lilli
Kuczyk, Markus Antonius
Bengel, Frank Michael
Peters, Inga
description Introduction The bone scan index (BSI) was introduced as a quantitative tool for tumor involvement in bone of patients with metastatic prostate cancer (mPCa). The computer-aided diagnosis device for BSI analysis EXINIbone BSI seems to represent technical progress for the quantitative assessment of bone involvement. But it is not yet clear if the automated BSI (aBSI) could contribute to improved evaluation of progression in patients under antiandrogens or chemotherapy in contrast to the visual interpretation and/or conventional biomarkers such as the prostate-specific antigen (PSA). Methods In 49 mPCa patients, bone scans were performed initially and during different therapy courses. Scans were evaluated visually and by the artificial-neural-network-based expert system EXINIbone BSI . Progression of metastatic bone involvement was defined according to the Prostate Cancer Clinical Trials Working Group 2 (PCWG2) criteria in the visual interpretation. The computer-assisted interpretation was based on different cutoff values in relative changes of the aBSI. Additionally, assessments according to bone scanning were compared to changes in the PSA value as a potential surrogate for treatment response. Results Using a sensitive cutoff value (5% or 10%) for the relative aBSI increase led to significantly increased progression determination compared to the visual interpretation of bone scans (49% and 43% vs. 27%, p  
doi_str_mv 10.1007/s12325-017-0505-z
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The computer-aided diagnosis device for BSI analysis EXINIbone BSI seems to represent technical progress for the quantitative assessment of bone involvement. But it is not yet clear if the automated BSI (aBSI) could contribute to improved evaluation of progression in patients under antiandrogens or chemotherapy in contrast to the visual interpretation and/or conventional biomarkers such as the prostate-specific antigen (PSA). Methods In 49 mPCa patients, bone scans were performed initially and during different therapy courses. Scans were evaluated visually and by the artificial-neural-network-based expert system EXINIbone BSI . Progression of metastatic bone involvement was defined according to the Prostate Cancer Clinical Trials Working Group 2 (PCWG2) criteria in the visual interpretation. The computer-assisted interpretation was based on different cutoff values in relative changes of the aBSI. Additionally, assessments according to bone scanning were compared to changes in the PSA value as a potential surrogate for treatment response. Results Using a sensitive cutoff value (5% or 10%) for the relative aBSI increase led to significantly increased progression determination compared to the visual interpretation of bone scans (49% and 43% vs. 27%, p  &lt; 0.001). In 63% of the cases PSA and BSI changes matched, whereas in 18% progression was only indicated by the aBSI. A relative cutoff of 5% for the aBSI decrease could reclassify 47 serial scan pairs which were visually interpreted as stable into 22 progressive and 25 remissive scans. Conclusion Distinct thresholds of the relative aBSI could help to better assess disease progression in mPCa patients. Manual corrections of the BSI values are not required in most cases. The aBSI could serve as a useful additional parameter for therapy monitoring in mPCa patients in the future.</description><identifier>ISSN: 0741-238X</identifier><identifier>EISSN: 1865-8652</identifier><identifier>DOI: 10.1007/s12325-017-0505-z</identifier><identifier>PMID: 28265811</identifier><language>eng</language><publisher>Cheshire: Springer Healthcare</publisher><subject>Aged ; Bone Neoplasms - diagnostic imaging ; Bone Neoplasms - secondary ; Cardiology ; Disease Progression ; Endocrinology ; Expert Systems ; Health technology assessment ; Humans ; Internal Medicine ; Male ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Oncology ; Original Research ; Pharmacology/Toxicology ; Prognosis ; Prostatic Neoplasms - pathology ; Radionuclide Imaging ; Retrospective Studies ; Rheumatology</subject><ispartof>Advances in therapy, 2017-04, Vol.34 (4), p.986-994</ispartof><rights>Springer Healthcare 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c410t-98937aaabcbf767efe90a4ca11010bc11c29e3deb470602338955047711676963</citedby><cites>FETCH-LOGICAL-c410t-98937aaabcbf767efe90a4ca11010bc11c29e3deb470602338955047711676963</cites><orcidid>0000-0002-2401-922X</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/s12325-017-0505-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12325-017-0505-z$$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/28265811$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Haupt, Fabian</creatorcontrib><creatorcontrib>Berding, Georg</creatorcontrib><creatorcontrib>Namazian, Ali</creatorcontrib><creatorcontrib>Wilke, Florian</creatorcontrib><creatorcontrib>Böker, Alena</creatorcontrib><creatorcontrib>Merseburger, Axel</creatorcontrib><creatorcontrib>Geworski, Lilli</creatorcontrib><creatorcontrib>Kuczyk, Markus Antonius</creatorcontrib><creatorcontrib>Bengel, Frank Michael</creatorcontrib><creatorcontrib>Peters, Inga</creatorcontrib><title>Expert System for Bone Scan Interpretation Improves Progression Assessment in Bone Metastatic Prostate Cancer</title><title>Advances in therapy</title><addtitle>Adv Ther</addtitle><addtitle>Adv Ther</addtitle><description>Introduction The bone scan index (BSI) was introduced as a quantitative tool for tumor involvement in bone of patients with metastatic prostate cancer (mPCa). The computer-aided diagnosis device for BSI analysis EXINIbone BSI seems to represent technical progress for the quantitative assessment of bone involvement. But it is not yet clear if the automated BSI (aBSI) could contribute to improved evaluation of progression in patients under antiandrogens or chemotherapy in contrast to the visual interpretation and/or conventional biomarkers such as the prostate-specific antigen (PSA). Methods In 49 mPCa patients, bone scans were performed initially and during different therapy courses. Scans were evaluated visually and by the artificial-neural-network-based expert system EXINIbone BSI . Progression of metastatic bone involvement was defined according to the Prostate Cancer Clinical Trials Working Group 2 (PCWG2) criteria in the visual interpretation. The computer-assisted interpretation was based on different cutoff values in relative changes of the aBSI. Additionally, assessments according to bone scanning were compared to changes in the PSA value as a potential surrogate for treatment response. Results Using a sensitive cutoff value (5% or 10%) for the relative aBSI increase led to significantly increased progression determination compared to the visual interpretation of bone scans (49% and 43% vs. 27%, p  &lt; 0.001). In 63% of the cases PSA and BSI changes matched, whereas in 18% progression was only indicated by the aBSI. A relative cutoff of 5% for the aBSI decrease could reclassify 47 serial scan pairs which were visually interpreted as stable into 22 progressive and 25 remissive scans. Conclusion Distinct thresholds of the relative aBSI could help to better assess disease progression in mPCa patients. Manual corrections of the BSI values are not required in most cases. 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Berding, Georg ; Namazian, Ali ; Wilke, Florian ; Böker, Alena ; Merseburger, Axel ; Geworski, Lilli ; Kuczyk, Markus Antonius ; Bengel, Frank Michael ; Peters, Inga</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c410t-98937aaabcbf767efe90a4ca11010bc11c29e3deb470602338955047711676963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Aged</topic><topic>Bone Neoplasms - diagnostic imaging</topic><topic>Bone Neoplasms - secondary</topic><topic>Cardiology</topic><topic>Disease Progression</topic><topic>Endocrinology</topic><topic>Expert Systems</topic><topic>Health technology assessment</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Middle Aged</topic><topic>Oncology</topic><topic>Original Research</topic><topic>Pharmacology/Toxicology</topic><topic>Prognosis</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Radionuclide Imaging</topic><topic>Retrospective Studies</topic><topic>Rheumatology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Haupt, Fabian</creatorcontrib><creatorcontrib>Berding, Georg</creatorcontrib><creatorcontrib>Namazian, Ali</creatorcontrib><creatorcontrib>Wilke, Florian</creatorcontrib><creatorcontrib>Böker, Alena</creatorcontrib><creatorcontrib>Merseburger, Axel</creatorcontrib><creatorcontrib>Geworski, Lilli</creatorcontrib><creatorcontrib>Kuczyk, Markus Antonius</creatorcontrib><creatorcontrib>Bengel, Frank Michael</creatorcontrib><creatorcontrib>Peters, Inga</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Advances in therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Haupt, Fabian</au><au>Berding, Georg</au><au>Namazian, Ali</au><au>Wilke, Florian</au><au>Böker, Alena</au><au>Merseburger, Axel</au><au>Geworski, Lilli</au><au>Kuczyk, Markus Antonius</au><au>Bengel, Frank Michael</au><au>Peters, Inga</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expert System for Bone Scan Interpretation Improves Progression Assessment in Bone Metastatic Prostate Cancer</atitle><jtitle>Advances in therapy</jtitle><stitle>Adv Ther</stitle><addtitle>Adv Ther</addtitle><date>2017-04-01</date><risdate>2017</risdate><volume>34</volume><issue>4</issue><spage>986</spage><epage>994</epage><pages>986-994</pages><issn>0741-238X</issn><eissn>1865-8652</eissn><abstract>Introduction The bone scan index (BSI) was introduced as a quantitative tool for tumor involvement in bone of patients with metastatic prostate cancer (mPCa). The computer-aided diagnosis device for BSI analysis EXINIbone BSI seems to represent technical progress for the quantitative assessment of bone involvement. But it is not yet clear if the automated BSI (aBSI) could contribute to improved evaluation of progression in patients under antiandrogens or chemotherapy in contrast to the visual interpretation and/or conventional biomarkers such as the prostate-specific antigen (PSA). Methods In 49 mPCa patients, bone scans were performed initially and during different therapy courses. Scans were evaluated visually and by the artificial-neural-network-based expert system EXINIbone BSI . Progression of metastatic bone involvement was defined according to the Prostate Cancer Clinical Trials Working Group 2 (PCWG2) criteria in the visual interpretation. The computer-assisted interpretation was based on different cutoff values in relative changes of the aBSI. Additionally, assessments according to bone scanning were compared to changes in the PSA value as a potential surrogate for treatment response. Results Using a sensitive cutoff value (5% or 10%) for the relative aBSI increase led to significantly increased progression determination compared to the visual interpretation of bone scans (49% and 43% vs. 27%, p  &lt; 0.001). In 63% of the cases PSA and BSI changes matched, whereas in 18% progression was only indicated by the aBSI. A relative cutoff of 5% for the aBSI decrease could reclassify 47 serial scan pairs which were visually interpreted as stable into 22 progressive and 25 remissive scans. Conclusion Distinct thresholds of the relative aBSI could help to better assess disease progression in mPCa patients. Manual corrections of the BSI values are not required in most cases. The aBSI could serve as a useful additional parameter for therapy monitoring in mPCa patients in the future.</abstract><cop>Cheshire</cop><pub>Springer Healthcare</pub><pmid>28265811</pmid><doi>10.1007/s12325-017-0505-z</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-2401-922X</orcidid></addata></record>
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subjects Aged
Bone Neoplasms - diagnostic imaging
Bone Neoplasms - secondary
Cardiology
Disease Progression
Endocrinology
Expert Systems
Health technology assessment
Humans
Internal Medicine
Male
Medicine
Medicine & Public Health
Middle Aged
Oncology
Original Research
Pharmacology/Toxicology
Prognosis
Prostatic Neoplasms - pathology
Radionuclide Imaging
Retrospective Studies
Rheumatology
title Expert System for Bone Scan Interpretation Improves Progression Assessment in Bone Metastatic Prostate Cancer
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