Pharmacokinetics of pretargeted monoclonal antibody 2D12.5 and 88Y-Janus-2-(p-nitrobenzyl)-1,4,7,10-tetraazacyclododecanetetraacetic acid (DOTA) in BALB/c mice with KHJJ mouse adenocarcinoma: a model for 90Y radioimmunotherapy

Three-step pretargeting for radioimmunotherapy in BALB/c mice with KHJJ tumors was done with monoclonal antibody (mAb) 2D12.5, which is specific for yttrium-1,4,7,10-tetraazacyclododecanetetraacetic acid (DOTA) but nonspecific for the tumor. Tumor uptake was by passive diffusion of mAb through leaky...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 1994-11, Vol.54 (22), p.5937-5946
Hauptverfasser: GOODWIN, D. A, MEARES, C. F, WATANABE, N, MCTIGUE, M, CHAOVAPONG, W, RANSONE, C. K, RENN, O, GREINER, D. P, KUKIS, D. L, KRONENBERGER, S. I
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container_issue 22
container_start_page 5937
container_title Cancer research (Chicago, Ill.)
container_volume 54
creator GOODWIN, D. A
MEARES, C. F
WATANABE, N
MCTIGUE, M
CHAOVAPONG, W
RANSONE, C. K
RENN, O
GREINER, D. P
KUKIS, D. L
KRONENBERGER, S. I
description Three-step pretargeting for radioimmunotherapy in BALB/c mice with KHJJ tumors was done with monoclonal antibody (mAb) 2D12.5, which is specific for yttrium-1,4,7,10-tetraazacyclododecanetetraacetic acid (DOTA) but nonspecific for the tumor. Tumor uptake was by passive diffusion of mAb through leaky neovasculature in the tumor. The three steps were: (a) anti-hapten mAb 2D12.5 (0 h); (b) polyvalent haptenprotein conjugate chase (20 h); and (c) 88Y-labeled monovalent DOTA or bivalent Janus-DOTA haptens (21 h) and organ and tumor bioassay (24 h). Rapid tumor (T) uptake and high tumor:blood ratio (T:BL) was seen 3 h after injection after step c. For monovalent 88Y-DOTA, T = 1.7%/g* and T:BL = 16:1; for bivalent 88Y-Janus-DOTA, T = 4.41%/g* and T:BL = 21:1 at 3 h (*, P < 0.001). Blood and bone plus marrow were 80% of injected dose. The biological half-life in the tumor of 0.9 microCi 88Y-Janus-DOTA was approximately 24 h, measured daily for 5 days. Activity in microCi/g of tumor and blood for 90Y equimolar to the amount of 88Y injected (0.9 microCi 88Y = 0.744 pmol = 36.47 microCi 90Y) was used for calculating the area under the curve of tumor and blood in microCi-h/g of 90Y. The 90Y radiation absorbed dose (RAD) from multiplying microCi-h/g x the 90Y absorbed dose constant, 1.99 RAD-g/microCi-h, gave T = 89 RAD and BL = 3.7 RAD. The therapeutic ratio from RAD T:RAD BL = 24:1. These results indicate that pretargeting 90Y hapten-specific mAb for radioimmunotherapy has considerable promise.
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A ; MEARES, C. F ; WATANABE, N ; MCTIGUE, M ; CHAOVAPONG, W ; RANSONE, C. K ; RENN, O ; GREINER, D. P ; KUKIS, D. L ; KRONENBERGER, S. I</creator><creatorcontrib>GOODWIN, D. A ; MEARES, C. F ; WATANABE, N ; MCTIGUE, M ; CHAOVAPONG, W ; RANSONE, C. K ; RENN, O ; GREINER, D. P ; KUKIS, D. L ; KRONENBERGER, S. I</creatorcontrib><description>Three-step pretargeting for radioimmunotherapy in BALB/c mice with KHJJ tumors was done with monoclonal antibody (mAb) 2D12.5, which is specific for yttrium-1,4,7,10-tetraazacyclododecanetetraacetic acid (DOTA) but nonspecific for the tumor. Tumor uptake was by passive diffusion of mAb through leaky neovasculature in the tumor. The three steps were: (a) anti-hapten mAb 2D12.5 (0 h); (b) polyvalent haptenprotein conjugate chase (20 h); and (c) 88Y-labeled monovalent DOTA or bivalent Janus-DOTA haptens (21 h) and organ and tumor bioassay (24 h). Rapid tumor (T) uptake and high tumor:blood ratio (T:BL) was seen 3 h after injection after step c. For monovalent 88Y-DOTA, T = 1.7%/g* and T:BL = 16:1; for bivalent 88Y-Janus-DOTA, T = 4.41%/g* and T:BL = 21:1 at 3 h (*, P &lt; 0.001). Blood and bone plus marrow were &lt;&lt; 1%/g, and liver was &lt; 1%/g. The 24-h whole body retention was approximately 5% of injected dose with 1% in tumor (20% of total), 1.8% in other organs, and 2.2% in carcass; the 24-h whole body retention of covalent nonspecific antibody conjugates was &gt; 80% of injected dose. The biological half-life in the tumor of 0.9 microCi 88Y-Janus-DOTA was approximately 24 h, measured daily for 5 days. Activity in microCi/g of tumor and blood for 90Y equimolar to the amount of 88Y injected (0.9 microCi 88Y = 0.744 pmol = 36.47 microCi 90Y) was used for calculating the area under the curve of tumor and blood in microCi-h/g of 90Y. The 90Y radiation absorbed dose (RAD) from multiplying microCi-h/g x the 90Y absorbed dose constant, 1.99 RAD-g/microCi-h, gave T = 89 RAD and BL = 3.7 RAD. The therapeutic ratio from RAD T:RAD BL = 24:1. These results indicate that pretargeting 90Y hapten-specific mAb for radioimmunotherapy has considerable promise.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 7954426</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Acetates - blood ; Acetates - pharmacokinetics ; Animals ; Antibodies, Monoclonal - blood ; Antibodies, Monoclonal - pharmacokinetics ; Biological and medical sciences ; Half-Life ; Heterocyclic Compounds - blood ; Heterocyclic Compounds - pharmacokinetics ; Mammary Neoplasms, Experimental - blood ; Mammary Neoplasms, Experimental - metabolism ; Mammary Neoplasms, Experimental - radiotherapy ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Radiation therapy and radiosensitizing agent ; Radioimmunotherapy - methods ; Tissue Distribution ; Treatment with physical agents ; Treatment. General aspects ; Tumors ; Yttrium Radioisotopes - blood ; Yttrium Radioisotopes - pharmacokinetics</subject><ispartof>Cancer research (Chicago, Ill.), 1994-11, Vol.54 (22), p.5937-5946</ispartof><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=3321686$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7954426$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>GOODWIN, D. A</creatorcontrib><creatorcontrib>MEARES, C. F</creatorcontrib><creatorcontrib>WATANABE, N</creatorcontrib><creatorcontrib>MCTIGUE, M</creatorcontrib><creatorcontrib>CHAOVAPONG, W</creatorcontrib><creatorcontrib>RANSONE, C. K</creatorcontrib><creatorcontrib>RENN, O</creatorcontrib><creatorcontrib>GREINER, D. P</creatorcontrib><creatorcontrib>KUKIS, D. L</creatorcontrib><creatorcontrib>KRONENBERGER, S. I</creatorcontrib><title>Pharmacokinetics of pretargeted monoclonal antibody 2D12.5 and 88Y-Janus-2-(p-nitrobenzyl)-1,4,7,10-tetraazacyclododecanetetraacetic acid (DOTA) in BALB/c mice with KHJJ mouse adenocarcinoma: a model for 90Y radioimmunotherapy</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>Three-step pretargeting for radioimmunotherapy in BALB/c mice with KHJJ tumors was done with monoclonal antibody (mAb) 2D12.5, which is specific for yttrium-1,4,7,10-tetraazacyclododecanetetraacetic acid (DOTA) but nonspecific for the tumor. Tumor uptake was by passive diffusion of mAb through leaky neovasculature in the tumor. The three steps were: (a) anti-hapten mAb 2D12.5 (0 h); (b) polyvalent haptenprotein conjugate chase (20 h); and (c) 88Y-labeled monovalent DOTA or bivalent Janus-DOTA haptens (21 h) and organ and tumor bioassay (24 h). Rapid tumor (T) uptake and high tumor:blood ratio (T:BL) was seen 3 h after injection after step c. For monovalent 88Y-DOTA, T = 1.7%/g* and T:BL = 16:1; for bivalent 88Y-Janus-DOTA, T = 4.41%/g* and T:BL = 21:1 at 3 h (*, P &lt; 0.001). Blood and bone plus marrow were &lt;&lt; 1%/g, and liver was &lt; 1%/g. The 24-h whole body retention was approximately 5% of injected dose with 1% in tumor (20% of total), 1.8% in other organs, and 2.2% in carcass; the 24-h whole body retention of covalent nonspecific antibody conjugates was &gt; 80% of injected dose. The biological half-life in the tumor of 0.9 microCi 88Y-Janus-DOTA was approximately 24 h, measured daily for 5 days. Activity in microCi/g of tumor and blood for 90Y equimolar to the amount of 88Y injected (0.9 microCi 88Y = 0.744 pmol = 36.47 microCi 90Y) was used for calculating the area under the curve of tumor and blood in microCi-h/g of 90Y. The 90Y radiation absorbed dose (RAD) from multiplying microCi-h/g x the 90Y absorbed dose constant, 1.99 RAD-g/microCi-h, gave T = 89 RAD and BL = 3.7 RAD. The therapeutic ratio from RAD T:RAD BL = 24:1. These results indicate that pretargeting 90Y hapten-specific mAb for radioimmunotherapy has considerable promise.</description><subject>Acetates - blood</subject><subject>Acetates - pharmacokinetics</subject><subject>Animals</subject><subject>Antibodies, Monoclonal - blood</subject><subject>Antibodies, Monoclonal - pharmacokinetics</subject><subject>Biological and medical sciences</subject><subject>Half-Life</subject><subject>Heterocyclic Compounds - blood</subject><subject>Heterocyclic Compounds - pharmacokinetics</subject><subject>Mammary Neoplasms, Experimental - blood</subject><subject>Mammary Neoplasms, Experimental - metabolism</subject><subject>Mammary Neoplasms, Experimental - radiotherapy</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Radiation therapy and radiosensitizing agent</subject><subject>Radioimmunotherapy - methods</subject><subject>Tissue Distribution</subject><subject>Treatment with physical agents</subject><subject>Treatment. General aspects</subject><subject>Tumors</subject><subject>Yttrium Radioisotopes - blood</subject><subject>Yttrium Radioisotopes - pharmacokinetics</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9UcFu1DAQjRCoLIVPQPIBoVZaQ-zYjre3bQuUZaVyKIeeVrP2hDUkdrAdofRz-RIMrDiN5r2nmTdvHlULJhtNWyHk42pR17WmUrT8afUspW-llayWJ9VJu5JCcLWofn0-QBzAhO_OY3YmkdCRMWKG-BUzWjIEH0wfPPQEfHb7YGfCrxl_I0tvidb3dAN-SpTTs5F6l2PYo3-Y-3PKlmLZLllNM-YI8ABmLpNssGigLPsLmj9LCRhnydn17d36nDhPLtfby7eGDM4g-enygXy62WyKkykhAYvFEETjfBjggkDBLfakC5Gs6nsSwbrghmHyIR8wwjg_r5500Cd8cayn1Zf37-6ubuj29sPHq_WWHhhTikquzAosA2bBdNII0QjRrpjVVnPEFrVsteIKFSu4VrA3rASKRvNV3aBqTqvX_-aOMfyYMOXd4JLBvi_HFuu7VpXUlWqK8OVROO0HtLsxugHivDs-pfCvjjwkA30XwRuX_suahjOlVfMb_HCWVA</recordid><startdate>19941115</startdate><enddate>19941115</enddate><creator>GOODWIN, D. A</creator><creator>MEARES, C. 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General aspects</topic><topic>Tumors</topic><topic>Yttrium Radioisotopes - blood</topic><topic>Yttrium Radioisotopes - pharmacokinetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GOODWIN, D. A</creatorcontrib><creatorcontrib>MEARES, C. F</creatorcontrib><creatorcontrib>WATANABE, N</creatorcontrib><creatorcontrib>MCTIGUE, M</creatorcontrib><creatorcontrib>CHAOVAPONG, W</creatorcontrib><creatorcontrib>RANSONE, C. K</creatorcontrib><creatorcontrib>RENN, O</creatorcontrib><creatorcontrib>GREINER, D. P</creatorcontrib><creatorcontrib>KUKIS, D. L</creatorcontrib><creatorcontrib>KRONENBERGER, S. I</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>GOODWIN, D. A</au><au>MEARES, C. F</au><au>WATANABE, N</au><au>MCTIGUE, M</au><au>CHAOVAPONG, W</au><au>RANSONE, C. K</au><au>RENN, O</au><au>GREINER, D. P</au><au>KUKIS, D. L</au><au>KRONENBERGER, S. I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pharmacokinetics of pretargeted monoclonal antibody 2D12.5 and 88Y-Janus-2-(p-nitrobenzyl)-1,4,7,10-tetraazacyclododecanetetraacetic acid (DOTA) in BALB/c mice with KHJJ mouse adenocarcinoma: a model for 90Y radioimmunotherapy</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1994-11-15</date><risdate>1994</risdate><volume>54</volume><issue>22</issue><spage>5937</spage><epage>5946</epage><pages>5937-5946</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>Three-step pretargeting for radioimmunotherapy in BALB/c mice with KHJJ tumors was done with monoclonal antibody (mAb) 2D12.5, which is specific for yttrium-1,4,7,10-tetraazacyclododecanetetraacetic acid (DOTA) but nonspecific for the tumor. Tumor uptake was by passive diffusion of mAb through leaky neovasculature in the tumor. The three steps were: (a) anti-hapten mAb 2D12.5 (0 h); (b) polyvalent haptenprotein conjugate chase (20 h); and (c) 88Y-labeled monovalent DOTA or bivalent Janus-DOTA haptens (21 h) and organ and tumor bioassay (24 h). Rapid tumor (T) uptake and high tumor:blood ratio (T:BL) was seen 3 h after injection after step c. For monovalent 88Y-DOTA, T = 1.7%/g* and T:BL = 16:1; for bivalent 88Y-Janus-DOTA, T = 4.41%/g* and T:BL = 21:1 at 3 h (*, P &lt; 0.001). Blood and bone plus marrow were &lt;&lt; 1%/g, and liver was &lt; 1%/g. The 24-h whole body retention was approximately 5% of injected dose with 1% in tumor (20% of total), 1.8% in other organs, and 2.2% in carcass; the 24-h whole body retention of covalent nonspecific antibody conjugates was &gt; 80% of injected dose. The biological half-life in the tumor of 0.9 microCi 88Y-Janus-DOTA was approximately 24 h, measured daily for 5 days. Activity in microCi/g of tumor and blood for 90Y equimolar to the amount of 88Y injected (0.9 microCi 88Y = 0.744 pmol = 36.47 microCi 90Y) was used for calculating the area under the curve of tumor and blood in microCi-h/g of 90Y. The 90Y radiation absorbed dose (RAD) from multiplying microCi-h/g x the 90Y absorbed dose constant, 1.99 RAD-g/microCi-h, gave T = 89 RAD and BL = 3.7 RAD. The therapeutic ratio from RAD T:RAD BL = 24:1. These results indicate that pretargeting 90Y hapten-specific mAb for radioimmunotherapy has considerable promise.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>7954426</pmid><tpages>10</tpages></addata></record>
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identifier ISSN: 0008-5472
ispartof Cancer research (Chicago, Ill.), 1994-11, Vol.54 (22), p.5937-5946
issn 0008-5472
1538-7445
language eng
recordid cdi_proquest_miscellaneous_76795663
source MEDLINE; American Association for Cancer Research Journals; EZB Electronic Journals Library
subjects Acetates - blood
Acetates - pharmacokinetics
Animals
Antibodies, Monoclonal - blood
Antibodies, Monoclonal - pharmacokinetics
Biological and medical sciences
Half-Life
Heterocyclic Compounds - blood
Heterocyclic Compounds - pharmacokinetics
Mammary Neoplasms, Experimental - blood
Mammary Neoplasms, Experimental - metabolism
Mammary Neoplasms, Experimental - radiotherapy
Medical sciences
Mice
Mice, Inbred BALB C
Radiation therapy and radiosensitizing agent
Radioimmunotherapy - methods
Tissue Distribution
Treatment with physical agents
Treatment. General aspects
Tumors
Yttrium Radioisotopes - blood
Yttrium Radioisotopes - pharmacokinetics
title Pharmacokinetics of pretargeted monoclonal antibody 2D12.5 and 88Y-Janus-2-(p-nitrobenzyl)-1,4,7,10-tetraazacyclododecanetetraacetic acid (DOTA) in BALB/c mice with KHJJ mouse adenocarcinoma: a model for 90Y radioimmunotherapy
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