Novel CYP11B-ligand [123/131I]IMAZA as promising theranostic tool for adrenocortical tumors: comprehensive preclinical characterization and first clinical experience
Purpose Adrenal tumors represent a diagnostic and therapeutic challenge. Promising results have been obtained through targeting the cytochrome P450 enzymes CYP11B1 and CYP11B2 for molecular imaging, and [ 123/131 I]iodometomidate ([ 123/131 I]IMTO) has even been successfully introduced as a theranos...
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Veröffentlicht in: | European journal of nuclear medicine and molecular imaging 2021-12, Vol.49 (1), p.301-310 |
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container_title | European journal of nuclear medicine and molecular imaging |
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creator | Heinze, Britta Schirbel, Andreas Nannen, Lukas Michelmann, David Hartrampf, Philipp E. Bluemel, Christina Schneider, Magdalena Herrmann, Ken Haenscheid, Heribert Fassnacht, Martin Buck, Andreas K. Hahner, Stefanie |
description | Purpose
Adrenal tumors represent a diagnostic and therapeutic challenge. Promising results have been obtained through targeting the cytochrome P450 enzymes CYP11B1 and CYP11B2 for molecular imaging, and [
123/131
I]iodometomidate ([
123/131
I]IMTO) has even been successfully introduced as a theranostic agent. As this radiopharmaceutical shows rapid metabolic inactivation, we aimed at developing new improved tracers.
Methods
Several IMTO derivatives were newly designed by replacing the unstable methyl ester by different carboxylic esters or amides. The inhibition of aldosterone and cortisol synthesis was tested in different adrenocortical cell lines. The corresponding radiolabeled compounds were assessed regarding their stability, in vitro cell uptake, in vivo biodistribution in mice, and their binding specificity to cryosections of human adrenocortical and non-adrenocortical tissue. Furthermore, a first investigation was performed in patients with known metastatic adrenal cancer using both [
123
I]IMTO and the most promising compound (R)-1-[1-(4-[
123
I]iodophenyl)ethyl]-1H-imidazole-5-carboxylic acid azetidinylamide ([
123
I]IMAZA) for scintigraphy. Subsequently, a first endoradiotherapy with [
131
I]IMAZA in one of these patients was performed.
Results
We identified three analogues to IMTO with high-affinity binding to the target enzymes and comparable or higher metabolic stability and very high and specific accumulation in adrenocortical cells in vitro and in vivo. Labeled IMAZA exhibited superior pharmacokinetic and imaging properties compared to IMTO in mice and 3 patients, too. An endoradiotherapy with [
131
I]IMAZA induced a 21-month progression-free interval in a patient with rapidly progressing ACC prior this therapy.
Conclusion
We developed the new radiopharmaceutical [
123/131
I]IMAZA with superior properties compared to the reference compound IMTO and promising first experiences in humans. |
doi_str_mv | 10.1007/s00259-021-05477-y |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8712301</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2614506015</sourcerecordid><originalsourceid>FETCH-LOGICAL-c441t-6a34a2daf5290c154ab495ab308aae48f4bee44d4aa0200968e50e8a83ae68763</originalsourceid><addsrcrecordid>eNp9kc2O0zAUhSMEYoaBF2CBLLEOc-04icMCqVT8VBp-FrAAhKxb56b1KLWD7VaU9-E98UyHAhtWtny-e86VT1E85PCEA7TnEUDUXQmCl1DLti33t4pT3vCubEF1t4_3Fk6KezFeAnAlVHe3OKmk4HUnxGnx863f0cjmn95z_rwc7Qpdz75wUZ3zii--Lt7MPs8YRjYFv7HRuhVLawrofEzWsOT9yAYfGPaBnDc-5FccWdpufIhPmfGbKdCaXLQ7yh5kRuuuCbPGgCZRsD8wWe_YVe5gQ0zsyND3KevkDN0v7gw4Rnpwc54VH1---DB_XV68e7WYzy5KIyVPZYOVRNHjUIsODK8lLmVX47IChUhSDXJJJGUvEUEAdI2iGkihqpAa1TbVWfHs4DttlxvqDbkUcNRTsBsMe-3R6n8VZ9d65XdatfnLgGeDxzcGwX_bUkz60m-Dyztr0XBZQwO8zpQ4UCb4GAMNxwQO-qpafahW52r1dbV6n4ce_b3bceR3lxmoDkDMkltR-JP9H9tfDQWzYg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2614506015</pqid></control><display><type>article</type><title>Novel CYP11B-ligand [123/131I]IMAZA as promising theranostic tool for adrenocortical tumors: comprehensive preclinical characterization and first clinical experience</title><source>MEDLINE</source><source>SpringerLink Journals</source><creator>Heinze, Britta ; Schirbel, Andreas ; Nannen, Lukas ; Michelmann, David ; Hartrampf, Philipp E. ; Bluemel, Christina ; Schneider, Magdalena ; Herrmann, Ken ; Haenscheid, Heribert ; Fassnacht, Martin ; Buck, Andreas K. ; Hahner, Stefanie</creator><creatorcontrib>Heinze, Britta ; Schirbel, Andreas ; Nannen, Lukas ; Michelmann, David ; Hartrampf, Philipp E. ; Bluemel, Christina ; Schneider, Magdalena ; Herrmann, Ken ; Haenscheid, Heribert ; Fassnacht, Martin ; Buck, Andreas K. ; Hahner, Stefanie</creatorcontrib><description>Purpose
Adrenal tumors represent a diagnostic and therapeutic challenge. Promising results have been obtained through targeting the cytochrome P450 enzymes CYP11B1 and CYP11B2 for molecular imaging, and [
123/131
I]iodometomidate ([
123/131
I]IMTO) has even been successfully introduced as a theranostic agent. As this radiopharmaceutical shows rapid metabolic inactivation, we aimed at developing new improved tracers.
Methods
Several IMTO derivatives were newly designed by replacing the unstable methyl ester by different carboxylic esters or amides. The inhibition of aldosterone and cortisol synthesis was tested in different adrenocortical cell lines. The corresponding radiolabeled compounds were assessed regarding their stability, in vitro cell uptake, in vivo biodistribution in mice, and their binding specificity to cryosections of human adrenocortical and non-adrenocortical tissue. Furthermore, a first investigation was performed in patients with known metastatic adrenal cancer using both [
123
I]IMTO and the most promising compound (R)-1-[1-(4-[
123
I]iodophenyl)ethyl]-1H-imidazole-5-carboxylic acid azetidinylamide ([
123
I]IMAZA) for scintigraphy. Subsequently, a first endoradiotherapy with [
131
I]IMAZA in one of these patients was performed.
Results
We identified three analogues to IMTO with high-affinity binding to the target enzymes and comparable or higher metabolic stability and very high and specific accumulation in adrenocortical cells in vitro and in vivo. Labeled IMAZA exhibited superior pharmacokinetic and imaging properties compared to IMTO in mice and 3 patients, too. An endoradiotherapy with [
131
I]IMAZA induced a 21-month progression-free interval in a patient with rapidly progressing ACC prior this therapy.
Conclusion
We developed the new radiopharmaceutical [
123/131
I]IMAZA with superior properties compared to the reference compound IMTO and promising first experiences in humans.</description><identifier>ISSN: 1619-7070</identifier><identifier>EISSN: 1619-7089</identifier><identifier>DOI: 10.1007/s00259-021-05477-y</identifier><identifier>PMID: 34215922</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adrenal Cortex Neoplasms - diagnostic imaging ; Adrenal Cortex Neoplasms - drug therapy ; Adrenocortical Carcinoma - diagnostic imaging ; Adrenocortical Carcinoma - drug therapy ; Aldosterone ; Aldosterone synthase ; Amides ; Animals ; Binding ; Carboxylic acids ; Cardiology ; Cortisol ; Cytochrome P450 ; Cytochromes P450 ; Enzymes ; Esters ; Humans ; Imaging ; Imidazole ; Ligands ; Medical imaging ; Medicine ; Medicine & Public Health ; Metabolism ; Metastases ; Mice ; Neuroendocrine tumors ; Nuclear Medicine ; Oncology ; Original ; Original Article ; Orthopedics ; Patients ; Pharmaceuticals ; Pharmacokinetics ; Precision Medicine ; Radiochemistry ; Radioisotopes ; Radiology ; Scintigraphy ; Stability analysis ; Steroid 11β-hydroxylase ; Theragnostic ; Tissue Distribution ; Tumors</subject><ispartof>European journal of nuclear medicine and molecular imaging, 2021-12, Vol.49 (1), p.301-310</ispartof><rights>The Author(s) 2021</rights><rights>2021. The Author(s).</rights><rights>The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-6a34a2daf5290c154ab495ab308aae48f4bee44d4aa0200968e50e8a83ae68763</citedby><cites>FETCH-LOGICAL-c441t-6a34a2daf5290c154ab495ab308aae48f4bee44d4aa0200968e50e8a83ae68763</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00259-021-05477-y$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00259-021-05477-y$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34215922$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Heinze, Britta</creatorcontrib><creatorcontrib>Schirbel, Andreas</creatorcontrib><creatorcontrib>Nannen, Lukas</creatorcontrib><creatorcontrib>Michelmann, David</creatorcontrib><creatorcontrib>Hartrampf, Philipp E.</creatorcontrib><creatorcontrib>Bluemel, Christina</creatorcontrib><creatorcontrib>Schneider, Magdalena</creatorcontrib><creatorcontrib>Herrmann, Ken</creatorcontrib><creatorcontrib>Haenscheid, Heribert</creatorcontrib><creatorcontrib>Fassnacht, Martin</creatorcontrib><creatorcontrib>Buck, Andreas K.</creatorcontrib><creatorcontrib>Hahner, Stefanie</creatorcontrib><title>Novel CYP11B-ligand [123/131I]IMAZA as promising theranostic tool for adrenocortical tumors: comprehensive preclinical characterization and first clinical experience</title><title>European journal of nuclear medicine and molecular imaging</title><addtitle>Eur J Nucl Med Mol Imaging</addtitle><addtitle>Eur J Nucl Med Mol Imaging</addtitle><description>Purpose
Adrenal tumors represent a diagnostic and therapeutic challenge. Promising results have been obtained through targeting the cytochrome P450 enzymes CYP11B1 and CYP11B2 for molecular imaging, and [
123/131
I]iodometomidate ([
123/131
I]IMTO) has even been successfully introduced as a theranostic agent. As this radiopharmaceutical shows rapid metabolic inactivation, we aimed at developing new improved tracers.
Methods
Several IMTO derivatives were newly designed by replacing the unstable methyl ester by different carboxylic esters or amides. The inhibition of aldosterone and cortisol synthesis was tested in different adrenocortical cell lines. The corresponding radiolabeled compounds were assessed regarding their stability, in vitro cell uptake, in vivo biodistribution in mice, and their binding specificity to cryosections of human adrenocortical and non-adrenocortical tissue. Furthermore, a first investigation was performed in patients with known metastatic adrenal cancer using both [
123
I]IMTO and the most promising compound (R)-1-[1-(4-[
123
I]iodophenyl)ethyl]-1H-imidazole-5-carboxylic acid azetidinylamide ([
123
I]IMAZA) for scintigraphy. Subsequently, a first endoradiotherapy with [
131
I]IMAZA in one of these patients was performed.
Results
We identified three analogues to IMTO with high-affinity binding to the target enzymes and comparable or higher metabolic stability and very high and specific accumulation in adrenocortical cells in vitro and in vivo. Labeled IMAZA exhibited superior pharmacokinetic and imaging properties compared to IMTO in mice and 3 patients, too. An endoradiotherapy with [
131
I]IMAZA induced a 21-month progression-free interval in a patient with rapidly progressing ACC prior this therapy.
Conclusion
We developed the new radiopharmaceutical [
123/131
I]IMAZA with superior properties compared to the reference compound IMTO and promising first experiences in humans.</description><subject>Adrenal Cortex Neoplasms - diagnostic imaging</subject><subject>Adrenal Cortex Neoplasms - drug therapy</subject><subject>Adrenocortical Carcinoma - diagnostic imaging</subject><subject>Adrenocortical Carcinoma - drug therapy</subject><subject>Aldosterone</subject><subject>Aldosterone synthase</subject><subject>Amides</subject><subject>Animals</subject><subject>Binding</subject><subject>Carboxylic acids</subject><subject>Cardiology</subject><subject>Cortisol</subject><subject>Cytochrome P450</subject><subject>Cytochromes P450</subject><subject>Enzymes</subject><subject>Esters</subject><subject>Humans</subject><subject>Imaging</subject><subject>Imidazole</subject><subject>Ligands</subject><subject>Medical imaging</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metabolism</subject><subject>Metastases</subject><subject>Mice</subject><subject>Neuroendocrine tumors</subject><subject>Nuclear Medicine</subject><subject>Oncology</subject><subject>Original</subject><subject>Original Article</subject><subject>Orthopedics</subject><subject>Patients</subject><subject>Pharmaceuticals</subject><subject>Pharmacokinetics</subject><subject>Precision Medicine</subject><subject>Radiochemistry</subject><subject>Radioisotopes</subject><subject>Radiology</subject><subject>Scintigraphy</subject><subject>Stability analysis</subject><subject>Steroid 11β-hydroxylase</subject><subject>Theragnostic</subject><subject>Tissue 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Britta</creator><creator>Schirbel, Andreas</creator><creator>Nannen, Lukas</creator><creator>Michelmann, David</creator><creator>Hartrampf, Philipp E.</creator><creator>Bluemel, Christina</creator><creator>Schneider, Magdalena</creator><creator>Herrmann, Ken</creator><creator>Haenscheid, Heribert</creator><creator>Fassnacht, Martin</creator><creator>Buck, Andreas K.</creator><creator>Hahner, Stefanie</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><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>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope></search><sort><creationdate>20211201</creationdate><title>Novel CYP11B-ligand [123/131I]IMAZA as promising theranostic tool for adrenocortical tumors: comprehensive preclinical characterization and first clinical experience</title><author>Heinze, Britta ; Schirbel, Andreas ; Nannen, Lukas ; Michelmann, David ; Hartrampf, Philipp E. ; Bluemel, Christina ; Schneider, Magdalena ; Herrmann, Ken ; Haenscheid, Heribert ; Fassnacht, Martin ; Buck, Andreas K. ; Hahner, Stefanie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-6a34a2daf5290c154ab495ab308aae48f4bee44d4aa0200968e50e8a83ae68763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adrenal Cortex Neoplasms - diagnostic imaging</topic><topic>Adrenal Cortex Neoplasms - drug therapy</topic><topic>Adrenocortical Carcinoma - diagnostic imaging</topic><topic>Adrenocortical Carcinoma - drug therapy</topic><topic>Aldosterone</topic><topic>Aldosterone synthase</topic><topic>Amides</topic><topic>Animals</topic><topic>Binding</topic><topic>Carboxylic acids</topic><topic>Cardiology</topic><topic>Cortisol</topic><topic>Cytochrome P450</topic><topic>Cytochromes P450</topic><topic>Enzymes</topic><topic>Esters</topic><topic>Humans</topic><topic>Imaging</topic><topic>Imidazole</topic><topic>Ligands</topic><topic>Medical imaging</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metabolism</topic><topic>Metastases</topic><topic>Mice</topic><topic>Neuroendocrine tumors</topic><topic>Nuclear Medicine</topic><topic>Oncology</topic><topic>Original</topic><topic>Original Article</topic><topic>Orthopedics</topic><topic>Patients</topic><topic>Pharmaceuticals</topic><topic>Pharmacokinetics</topic><topic>Precision Medicine</topic><topic>Radiochemistry</topic><topic>Radioisotopes</topic><topic>Radiology</topic><topic>Scintigraphy</topic><topic>Stability analysis</topic><topic>Steroid 11β-hydroxylase</topic><topic>Theragnostic</topic><topic>Tissue Distribution</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Heinze, Britta</creatorcontrib><creatorcontrib>Schirbel, Andreas</creatorcontrib><creatorcontrib>Nannen, Lukas</creatorcontrib><creatorcontrib>Michelmann, David</creatorcontrib><creatorcontrib>Hartrampf, Philipp E.</creatorcontrib><creatorcontrib>Bluemel, Christina</creatorcontrib><creatorcontrib>Schneider, Magdalena</creatorcontrib><creatorcontrib>Herrmann, Ken</creatorcontrib><creatorcontrib>Haenscheid, Heribert</creatorcontrib><creatorcontrib>Fassnacht, Martin</creatorcontrib><creatorcontrib>Buck, Andreas K.</creatorcontrib><creatorcontrib>Hahner, Stefanie</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE 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Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>European journal of nuclear medicine and molecular imaging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Heinze, Britta</au><au>Schirbel, Andreas</au><au>Nannen, Lukas</au><au>Michelmann, David</au><au>Hartrampf, Philipp E.</au><au>Bluemel, Christina</au><au>Schneider, Magdalena</au><au>Herrmann, Ken</au><au>Haenscheid, Heribert</au><au>Fassnacht, Martin</au><au>Buck, Andreas K.</au><au>Hahner, Stefanie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel CYP11B-ligand [123/131I]IMAZA as promising theranostic tool for adrenocortical tumors: comprehensive preclinical characterization and first clinical experience</atitle><jtitle>European journal of nuclear medicine and molecular imaging</jtitle><stitle>Eur J Nucl Med Mol Imaging</stitle><addtitle>Eur J Nucl Med Mol Imaging</addtitle><date>2021-12-01</date><risdate>2021</risdate><volume>49</volume><issue>1</issue><spage>301</spage><epage>310</epage><pages>301-310</pages><issn>1619-7070</issn><eissn>1619-7089</eissn><abstract>Purpose
Adrenal tumors represent a diagnostic and therapeutic challenge. Promising results have been obtained through targeting the cytochrome P450 enzymes CYP11B1 and CYP11B2 for molecular imaging, and [
123/131
I]iodometomidate ([
123/131
I]IMTO) has even been successfully introduced as a theranostic agent. As this radiopharmaceutical shows rapid metabolic inactivation, we aimed at developing new improved tracers.
Methods
Several IMTO derivatives were newly designed by replacing the unstable methyl ester by different carboxylic esters or amides. The inhibition of aldosterone and cortisol synthesis was tested in different adrenocortical cell lines. The corresponding radiolabeled compounds were assessed regarding their stability, in vitro cell uptake, in vivo biodistribution in mice, and their binding specificity to cryosections of human adrenocortical and non-adrenocortical tissue. Furthermore, a first investigation was performed in patients with known metastatic adrenal cancer using both [
123
I]IMTO and the most promising compound (R)-1-[1-(4-[
123
I]iodophenyl)ethyl]-1H-imidazole-5-carboxylic acid azetidinylamide ([
123
I]IMAZA) for scintigraphy. Subsequently, a first endoradiotherapy with [
131
I]IMAZA in one of these patients was performed.
Results
We identified three analogues to IMTO with high-affinity binding to the target enzymes and comparable or higher metabolic stability and very high and specific accumulation in adrenocortical cells in vitro and in vivo. Labeled IMAZA exhibited superior pharmacokinetic and imaging properties compared to IMTO in mice and 3 patients, too. An endoradiotherapy with [
131
I]IMAZA induced a 21-month progression-free interval in a patient with rapidly progressing ACC prior this therapy.
Conclusion
We developed the new radiopharmaceutical [
123/131
I]IMAZA with superior properties compared to the reference compound IMTO and promising first experiences in humans.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>34215922</pmid><doi>10.1007/s00259-021-05477-y</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; SpringerLink Journals |
subjects | Adrenal Cortex Neoplasms - diagnostic imaging Adrenal Cortex Neoplasms - drug therapy Adrenocortical Carcinoma - diagnostic imaging Adrenocortical Carcinoma - drug therapy Aldosterone Aldosterone synthase Amides Animals Binding Carboxylic acids Cardiology Cortisol Cytochrome P450 Cytochromes P450 Enzymes Esters Humans Imaging Imidazole Ligands Medical imaging Medicine Medicine & Public Health Metabolism Metastases Mice Neuroendocrine tumors Nuclear Medicine Oncology Original Original Article Orthopedics Patients Pharmaceuticals Pharmacokinetics Precision Medicine Radiochemistry Radioisotopes Radiology Scintigraphy Stability analysis Steroid 11β-hydroxylase Theragnostic Tissue Distribution Tumors |
title | Novel CYP11B-ligand [123/131I]IMAZA as promising theranostic tool for adrenocortical tumors: comprehensive preclinical characterization and first clinical experience |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T00%3A41%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Novel%20CYP11B-ligand%20%5B123/131I%5DIMAZA%20as%20promising%20theranostic%20tool%20for%20adrenocortical%20tumors:%20comprehensive%20preclinical%20characterization%20and%20first%20clinical%20experience&rft.jtitle=European%20journal%20of%20nuclear%20medicine%20and%20molecular%20imaging&rft.au=Heinze,%20Britta&rft.date=2021-12-01&rft.volume=49&rft.issue=1&rft.spage=301&rft.epage=310&rft.pages=301-310&rft.issn=1619-7070&rft.eissn=1619-7089&rft_id=info:doi/10.1007/s00259-021-05477-y&rft_dat=%3Cproquest_pubme%3E2614506015%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2614506015&rft_id=info:pmid/34215922&rfr_iscdi=true |