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Treatment response evaluation with 18F-FDG PET/CT and 18F-NaF PET/CT in multiple myeloma patients undergoing high-dose chemotherapy and autologous stem cell transplantation

Aim The aim of this study was to assess the combined use of the radiotracers 18 F-FDG and 18 F-NaF in treatment response evaluation of a group of multiple myeloma (MM) patients undergoing high-dose chemotherapy (HDT) followed by autologous stem cell transplantation (ASCT) by means of static (whole-b...

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Published in:European journal of nuclear medicine and molecular imaging 2017, Vol.44 (1), p.50-62
Main Authors: Sachpekidis, Christos, Hillengass, J., Goldschmidt, H., Wagner, B., Haberkorn, U., Kopka, K., Dimitrakopoulou-Strauss, A.
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creator Sachpekidis, Christos
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description Aim The aim of this study was to assess the combined use of the radiotracers 18 F-FDG and 18 F-NaF in treatment response evaluation of a group of multiple myeloma (MM) patients undergoing high-dose chemotherapy (HDT) followed by autologous stem cell transplantation (ASCT) by means of static (whole-body) and dynamic PET/CT (dPET/CT). Patients and methods Thirty-four patients with primary, previously untreated MM scheduled for treatment with HDT followed by ASCT were enrolled in the study. All patients underwent PET/CT scanning with 18 F-FDG and 18 F-NaF before and after therapy. Treatment response by means of PET/CT was assessed according to the European Organization for Research and Treatment of Cancer (EORTC) 1999 criteria. The evaluation of dPET/CT studies was based on qualitative evaluation, semi-quantitative (SUV) calculation, and quantitative analysis based on two-tissue compartment modelling and a non-compartmental approach leading to the extraction of fractal dimension (FD). Results An analysis was possible in 29 patients: three with clinical complete response (CR) and 26 with non-CR (13 patients near complete response-nCR, four patients very good partial response-VGPR, nine patients partial response-PR). After treatment, 18 F-FDG PET/CT was negative in 14/29 patients and positive in 15/29 patients, showing a sensitivity of 57.5 % and a specificity of 100 %. According to the EORTC 1999 criteria, 18 F-FDG PET/CT-based treatment response revealed CR in 14 patients ( 18 F-FDG PET/CT CR), PR in 11 patients ( 18 F-FDG PET/CT PR) and progressive disease in four patients ( 18 F-FDG PET/CT PD). In terms of 18 F-NaF PET/CT, 4/29 patients (13.8 %) had a negative baseline scan, thus failed to depict MM. Regarding the patients for which a direct lesion-to-lesion comparison was feasible, 18 F-NaF PET/CT depicted 56 of the 129 18 F-FDG positive lesions (43 %). Follow-up 18 F-NaF PET/CT showed persistence of 81.5 % of the baseline 18 F-NaF positive MM lesions after treatment, despite the fact that 64.7 % of them had turned to 18 F-FDG negative. Treatment response according to 18 F-NaF PET/CT revealed CR in one patient ( 18 F-NaF PET/CT CR), PR in five patients ( 18 F-NaF PET/CT PR), SD in 12 patients ( 18 F-NaF PET/CT SD), and PD in seven patients ( 18 F-NaF PET/CT PD). Dynamic 18 F-FDG and 18 F-NaF PET/CT studies showed that SUV average , SUV max , as well as the kinetic parameters K 1 , influx and FD from reference bone marrow and skeleton responded to therapy w
doi_str_mv 10.1007/s00259-016-3502-6
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Patients and methods Thirty-four patients with primary, previously untreated MM scheduled for treatment with HDT followed by ASCT were enrolled in the study. All patients underwent PET/CT scanning with 18 F-FDG and 18 F-NaF before and after therapy. Treatment response by means of PET/CT was assessed according to the European Organization for Research and Treatment of Cancer (EORTC) 1999 criteria. The evaluation of dPET/CT studies was based on qualitative evaluation, semi-quantitative (SUV) calculation, and quantitative analysis based on two-tissue compartment modelling and a non-compartmental approach leading to the extraction of fractal dimension (FD). Results An analysis was possible in 29 patients: three with clinical complete response (CR) and 26 with non-CR (13 patients near complete response-nCR, four patients very good partial response-VGPR, nine patients partial response-PR). After treatment, 18 F-FDG PET/CT was negative in 14/29 patients and positive in 15/29 patients, showing a sensitivity of 57.5 % and a specificity of 100 %. According to the EORTC 1999 criteria, 18 F-FDG PET/CT-based treatment response revealed CR in 14 patients ( 18 F-FDG PET/CT CR), PR in 11 patients ( 18 F-FDG PET/CT PR) and progressive disease in four patients ( 18 F-FDG PET/CT PD). In terms of 18 F-NaF PET/CT, 4/29 patients (13.8 %) had a negative baseline scan, thus failed to depict MM. Regarding the patients for which a direct lesion-to-lesion comparison was feasible, 18 F-NaF PET/CT depicted 56 of the 129 18 F-FDG positive lesions (43 %). Follow-up 18 F-NaF PET/CT showed persistence of 81.5 % of the baseline 18 F-NaF positive MM lesions after treatment, despite the fact that 64.7 % of them had turned to 18 F-FDG negative. Treatment response according to 18 F-NaF PET/CT revealed CR in one patient ( 18 F-NaF PET/CT CR), PR in five patients ( 18 F-NaF PET/CT PR), SD in 12 patients ( 18 F-NaF PET/CT SD), and PD in seven patients ( 18 F-NaF PET/CT PD). Dynamic 18 F-FDG and 18 F-NaF PET/CT studies showed that SUV average , SUV max , as well as the kinetic parameters K 1 , influx and FD from reference bone marrow and skeleton responded to therapy with a significant decrease ( p  &lt; 0.001). Conclusion F-FDG PET/CT demonstrated a sensitivity of 57.7 % and a specificity of 100 % in treatment response evaluation of MM. Despite its limited sensitivity, the performance of 18 F-FDG PET/CT was satisfactory, given that 6/9 false negative patients in follow-up scans (66.7 %) were clinically characterized as nCR, a disease stage with very low tumor mass. On the other hand, 18 F-NaF PET/CT does not seem to add significantly to 18 F-FDG PET/CT in treatment response evaluation of MM patients undergoing HDT and ASCT, at least shortly after therapy.</description><identifier>ISSN: 1619-7070</identifier><identifier>EISSN: 1619-7089</identifier><identifier>DOI: 10.1007/s00259-016-3502-6</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Cardiology ; Imaging ; Medicine ; Medicine &amp; Public Health ; Nuclear Medicine ; Oncology ; Original Article ; Orthopedics ; Radiology</subject><ispartof>European journal of nuclear medicine and molecular imaging, 2017, Vol.44 (1), p.50-62</ispartof><rights>Springer-Verlag Berlin Heidelberg 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2096-f3276fa3adab32b306102a1577c8e5c669df1b61887cb65ee2d03ffed8b3fd143</citedby><cites>FETCH-LOGICAL-c2096-f3276fa3adab32b306102a1577c8e5c669df1b61887cb65ee2d03ffed8b3fd143</cites><orcidid>0000-0001-8739-8741</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Sachpekidis, Christos</creatorcontrib><creatorcontrib>Hillengass, J.</creatorcontrib><creatorcontrib>Goldschmidt, H.</creatorcontrib><creatorcontrib>Wagner, B.</creatorcontrib><creatorcontrib>Haberkorn, U.</creatorcontrib><creatorcontrib>Kopka, K.</creatorcontrib><creatorcontrib>Dimitrakopoulou-Strauss, A.</creatorcontrib><title>Treatment response evaluation with 18F-FDG PET/CT and 18F-NaF PET/CT in multiple myeloma patients undergoing high-dose chemotherapy and autologous stem cell transplantation</title><title>European journal of nuclear medicine and molecular imaging</title><addtitle>Eur J Nucl Med Mol Imaging</addtitle><description>Aim The aim of this study was to assess the combined use of the radiotracers 18 F-FDG and 18 F-NaF in treatment response evaluation of a group of multiple myeloma (MM) patients undergoing high-dose chemotherapy (HDT) followed by autologous stem cell transplantation (ASCT) by means of static (whole-body) and dynamic PET/CT (dPET/CT). Patients and methods Thirty-four patients with primary, previously untreated MM scheduled for treatment with HDT followed by ASCT were enrolled in the study. All patients underwent PET/CT scanning with 18 F-FDG and 18 F-NaF before and after therapy. Treatment response by means of PET/CT was assessed according to the European Organization for Research and Treatment of Cancer (EORTC) 1999 criteria. The evaluation of dPET/CT studies was based on qualitative evaluation, semi-quantitative (SUV) calculation, and quantitative analysis based on two-tissue compartment modelling and a non-compartmental approach leading to the extraction of fractal dimension (FD). Results An analysis was possible in 29 patients: three with clinical complete response (CR) and 26 with non-CR (13 patients near complete response-nCR, four patients very good partial response-VGPR, nine patients partial response-PR). After treatment, 18 F-FDG PET/CT was negative in 14/29 patients and positive in 15/29 patients, showing a sensitivity of 57.5 % and a specificity of 100 %. According to the EORTC 1999 criteria, 18 F-FDG PET/CT-based treatment response revealed CR in 14 patients ( 18 F-FDG PET/CT CR), PR in 11 patients ( 18 F-FDG PET/CT PR) and progressive disease in four patients ( 18 F-FDG PET/CT PD). In terms of 18 F-NaF PET/CT, 4/29 patients (13.8 %) had a negative baseline scan, thus failed to depict MM. Regarding the patients for which a direct lesion-to-lesion comparison was feasible, 18 F-NaF PET/CT depicted 56 of the 129 18 F-FDG positive lesions (43 %). Follow-up 18 F-NaF PET/CT showed persistence of 81.5 % of the baseline 18 F-NaF positive MM lesions after treatment, despite the fact that 64.7 % of them had turned to 18 F-FDG negative. Treatment response according to 18 F-NaF PET/CT revealed CR in one patient ( 18 F-NaF PET/CT CR), PR in five patients ( 18 F-NaF PET/CT PR), SD in 12 patients ( 18 F-NaF PET/CT SD), and PD in seven patients ( 18 F-NaF PET/CT PD). Dynamic 18 F-FDG and 18 F-NaF PET/CT studies showed that SUV average , SUV max , as well as the kinetic parameters K 1 , influx and FD from reference bone marrow and skeleton responded to therapy with a significant decrease ( p  &lt; 0.001). Conclusion F-FDG PET/CT demonstrated a sensitivity of 57.7 % and a specificity of 100 % in treatment response evaluation of MM. Despite its limited sensitivity, the performance of 18 F-FDG PET/CT was satisfactory, given that 6/9 false negative patients in follow-up scans (66.7 %) were clinically characterized as nCR, a disease stage with very low tumor mass. On the other hand, 18 F-NaF PET/CT does not seem to add significantly to 18 F-FDG PET/CT in treatment response evaluation of MM patients undergoing HDT and ASCT, at least shortly after therapy.</description><subject>Cardiology</subject><subject>Imaging</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Nuclear Medicine</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Orthopedics</subject><subject>Radiology</subject><issn>1619-7070</issn><issn>1619-7089</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9Ubtu3DAQFAIbiF8fkI6lG8Z8nCiqDC4-x4BhuzjXxEpaPQyKlEkqwf2TPzK6Oyelq10MZmZnMVn2jbPvnLHiJjIm8pIyrqjMmaDqS3bGFS9pwXR58n8v2NfsPMZXxrgWujzL3rcBIY3oEgkYJ-8iEvwNdoY0eEf-DKknXG_o5ucdeb7d3qy3BFxzgB5h8w8aHBlnm4bJIhl3aP0IZFocFttIZtdg6PzgOtIPXU8bv9yoexx96jHAtDs4wpy89Z2fI4kJR1KjtSQFcHGy4NIhzmV22oKNePUxL7KXze12_Ys-PN3dr3880FqwUtFWikK1IKGBSopKMsWZAJ4XRa0xr5Uqm5ZXimtd1JXKEUXDZNtioyvZNnwlL7Lro-8U_NuMMZlxiPtA4HAJaLheyZJLuVILlR-pdfAxBmzNFIYRws5wZvbNmGMzZmnG7Jsxe404auLCdR0G8-rn4JaPPhH9Bednk0Q</recordid><startdate>2017</startdate><enddate>2017</enddate><creator>Sachpekidis, Christos</creator><creator>Hillengass, J.</creator><creator>Goldschmidt, H.</creator><creator>Wagner, B.</creator><creator>Haberkorn, U.</creator><creator>Kopka, K.</creator><creator>Dimitrakopoulou-Strauss, A.</creator><general>Springer Berlin Heidelberg</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8739-8741</orcidid></search><sort><creationdate>2017</creationdate><title>Treatment response evaluation with 18F-FDG PET/CT and 18F-NaF PET/CT in multiple myeloma patients undergoing high-dose chemotherapy and autologous stem cell transplantation</title><author>Sachpekidis, Christos ; Hillengass, J. ; Goldschmidt, H. ; Wagner, B. ; Haberkorn, U. ; Kopka, K. ; Dimitrakopoulou-Strauss, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2096-f3276fa3adab32b306102a1577c8e5c669df1b61887cb65ee2d03ffed8b3fd143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Cardiology</topic><topic>Imaging</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Nuclear Medicine</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Orthopedics</topic><topic>Radiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sachpekidis, Christos</creatorcontrib><creatorcontrib>Hillengass, J.</creatorcontrib><creatorcontrib>Goldschmidt, H.</creatorcontrib><creatorcontrib>Wagner, B.</creatorcontrib><creatorcontrib>Haberkorn, U.</creatorcontrib><creatorcontrib>Kopka, K.</creatorcontrib><creatorcontrib>Dimitrakopoulou-Strauss, A.</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of nuclear medicine and molecular imaging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sachpekidis, Christos</au><au>Hillengass, J.</au><au>Goldschmidt, H.</au><au>Wagner, B.</au><au>Haberkorn, U.</au><au>Kopka, K.</au><au>Dimitrakopoulou-Strauss, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Treatment response evaluation with 18F-FDG PET/CT and 18F-NaF PET/CT in multiple myeloma patients undergoing high-dose chemotherapy and autologous stem cell transplantation</atitle><jtitle>European journal of nuclear medicine and molecular imaging</jtitle><stitle>Eur J Nucl Med Mol Imaging</stitle><date>2017</date><risdate>2017</risdate><volume>44</volume><issue>1</issue><spage>50</spage><epage>62</epage><pages>50-62</pages><issn>1619-7070</issn><eissn>1619-7089</eissn><abstract>Aim The aim of this study was to assess the combined use of the radiotracers 18 F-FDG and 18 F-NaF in treatment response evaluation of a group of multiple myeloma (MM) patients undergoing high-dose chemotherapy (HDT) followed by autologous stem cell transplantation (ASCT) by means of static (whole-body) and dynamic PET/CT (dPET/CT). Patients and methods Thirty-four patients with primary, previously untreated MM scheduled for treatment with HDT followed by ASCT were enrolled in the study. All patients underwent PET/CT scanning with 18 F-FDG and 18 F-NaF before and after therapy. Treatment response by means of PET/CT was assessed according to the European Organization for Research and Treatment of Cancer (EORTC) 1999 criteria. The evaluation of dPET/CT studies was based on qualitative evaluation, semi-quantitative (SUV) calculation, and quantitative analysis based on two-tissue compartment modelling and a non-compartmental approach leading to the extraction of fractal dimension (FD). Results An analysis was possible in 29 patients: three with clinical complete response (CR) and 26 with non-CR (13 patients near complete response-nCR, four patients very good partial response-VGPR, nine patients partial response-PR). After treatment, 18 F-FDG PET/CT was negative in 14/29 patients and positive in 15/29 patients, showing a sensitivity of 57.5 % and a specificity of 100 %. According to the EORTC 1999 criteria, 18 F-FDG PET/CT-based treatment response revealed CR in 14 patients ( 18 F-FDG PET/CT CR), PR in 11 patients ( 18 F-FDG PET/CT PR) and progressive disease in four patients ( 18 F-FDG PET/CT PD). In terms of 18 F-NaF PET/CT, 4/29 patients (13.8 %) had a negative baseline scan, thus failed to depict MM. Regarding the patients for which a direct lesion-to-lesion comparison was feasible, 18 F-NaF PET/CT depicted 56 of the 129 18 F-FDG positive lesions (43 %). Follow-up 18 F-NaF PET/CT showed persistence of 81.5 % of the baseline 18 F-NaF positive MM lesions after treatment, despite the fact that 64.7 % of them had turned to 18 F-FDG negative. Treatment response according to 18 F-NaF PET/CT revealed CR in one patient ( 18 F-NaF PET/CT CR), PR in five patients ( 18 F-NaF PET/CT PR), SD in 12 patients ( 18 F-NaF PET/CT SD), and PD in seven patients ( 18 F-NaF PET/CT PD). Dynamic 18 F-FDG and 18 F-NaF PET/CT studies showed that SUV average , SUV max , as well as the kinetic parameters K 1 , influx and FD from reference bone marrow and skeleton responded to therapy with a significant decrease ( p  &lt; 0.001). Conclusion F-FDG PET/CT demonstrated a sensitivity of 57.7 % and a specificity of 100 % in treatment response evaluation of MM. Despite its limited sensitivity, the performance of 18 F-FDG PET/CT was satisfactory, given that 6/9 false negative patients in follow-up scans (66.7 %) were clinically characterized as nCR, a disease stage with very low tumor mass. On the other hand, 18 F-NaF PET/CT does not seem to add significantly to 18 F-FDG PET/CT in treatment response evaluation of MM patients undergoing HDT and ASCT, at least shortly after therapy.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><doi>10.1007/s00259-016-3502-6</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-8739-8741</orcidid><oa>free_for_read</oa></addata></record>
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subjects Cardiology
Imaging
Medicine
Medicine & Public Health
Nuclear Medicine
Oncology
Original Article
Orthopedics
Radiology
title Treatment response evaluation with 18F-FDG PET/CT and 18F-NaF PET/CT in multiple myeloma patients undergoing high-dose chemotherapy and autologous stem cell transplantation
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