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
Hauptverfasser: 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
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container_issue 1
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container_title European journal of nuclear medicine and molecular imaging
container_volume 49
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
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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 &amp; 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”). 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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. 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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 &amp; 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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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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
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