Antibody distribution and dosimetry in patients receiving radiolabelled antibody therapy for colorectal cancer: Clinical Oncology/Epidemiology
The distribution of iodine-131 (131I) labelled antibody to carcinoembryonic antigen (CEA) has been studied in 16 patients with colorectal cancer. Levels of tumour and normal tissue radioactivity were measured by serial gamma-camera imaging and counting of blood and urine. Maximum concentrations were...
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Veröffentlicht in: | British journal of cancer 1989-09, Vol.60 (3), p.406-412 |
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description | The distribution of iodine-131 (131I) labelled antibody to carcinoembryonic antigen (CEA) has been studied in 16 patients with colorectal cancer. Levels of tumour and normal tissue radioactivity were measured by serial gamma-camera imaging and counting of blood and urine. Maximum concentrations were found in tumour 8 h after administration and varied up to 9-fold in different patients. Higher levels were found on average in tumour than in any other tissue. Liver, lung and blood were the other tissues in which antibody was concentrated relative to the rest of the body. Antibody cleared from all these tissues over 1 week. Second antibody directed against the antitumour (first) antibody was given 24 h after first antibody in order to accelerate clearance from the blood. This increased the tumour to blood ratio but had little effect on other tissues. Cumulative radiation dose to tumour and normal tissue was estimated. In patients with the most efficient localisation the tumour to body ratio was 20:1 and tumour to blood ratio 5:1. This may be sufficient for effective therapy of cancer in patients selected for efficient antibody localisation. The data may be used to estimate the effect of different therapeutic strategies. For instance, in the time after second antibody administration the average tumour to blood ratio of radiation dose was 11:1, suggesting that two phase systems in which the therapeutic modality is given after a good tumour to normal tissue ratio is obtained may be effective for the majority of patients. |
doi_str_mv | 10.1038/bjc.1989.295 |
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Levels of tumour and normal tissue radioactivity were measured by serial gamma-camera imaging and counting of blood and urine. Maximum concentrations were found in tumour 8 h after administration and varied up to 9-fold in different patients. Higher levels were found on average in tumour than in any other tissue. Liver, lung and blood were the other tissues in which antibody was concentrated relative to the rest of the body. Antibody cleared from all these tissues over 1 week. Second antibody directed against the antitumour (first) antibody was given 24 h after first antibody in order to accelerate clearance from the blood. This increased the tumour to blood ratio but had little effect on other tissues. Cumulative radiation dose to tumour and normal tissue was estimated. In patients with the most efficient localisation the tumour to body ratio was 20:1 and tumour to blood ratio 5:1. This may be sufficient for effective therapy of cancer in patients selected for efficient antibody localisation. The data may be used to estimate the effect of different therapeutic strategies. For instance, in the time after second antibody administration the average tumour to blood ratio of radiation dose was 11:1, suggesting that two phase systems in which the therapeutic modality is given after a good tumour to normal tissue ratio is obtained may be effective for the majority of patients.</description><identifier>ISSN: 0007-0920</identifier><identifier>EISSN: 1532-1827</identifier><identifier>DOI: 10.1038/bjc.1989.295</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; clinical-oncology-epidemiology ; Drug Resistance ; Epidemiology ; Molecular Medicine ; Oncology</subject><ispartof>British journal of cancer, 1989-09, Vol.60 (3), p.406-412</ispartof><rights>Cancer Research Campaign 1989</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/bjc.1989.295$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/bjc.1989.295$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids></links><search><creatorcontrib>Begent, RHJ</creatorcontrib><creatorcontrib>Ledermann, JA</creatorcontrib><creatorcontrib>Green, AJ</creatorcontrib><creatorcontrib>Bagshawe, KD</creatorcontrib><creatorcontrib>Riggs, SJ</creatorcontrib><creatorcontrib>Searle, F</creatorcontrib><creatorcontrib>Keep, PA</creatorcontrib><creatorcontrib>Adam, T</creatorcontrib><creatorcontrib>Dale, RG</creatorcontrib><creatorcontrib>Glaser, MG</creatorcontrib><title>Antibody distribution and dosimetry in patients receiving radiolabelled antibody therapy for colorectal cancer: Clinical Oncology/Epidemiology</title><title>British journal of cancer</title><addtitle>Br J Cancer</addtitle><description>The distribution of iodine-131 (131I) labelled antibody to carcinoembryonic antigen (CEA) has been studied in 16 patients with colorectal cancer. Levels of tumour and normal tissue radioactivity were measured by serial gamma-camera imaging and counting of blood and urine. Maximum concentrations were found in tumour 8 h after administration and varied up to 9-fold in different patients. Higher levels were found on average in tumour than in any other tissue. Liver, lung and blood were the other tissues in which antibody was concentrated relative to the rest of the body. Antibody cleared from all these tissues over 1 week. Second antibody directed against the antitumour (first) antibody was given 24 h after first antibody in order to accelerate clearance from the blood. This increased the tumour to blood ratio but had little effect on other tissues. Cumulative radiation dose to tumour and normal tissue was estimated. In patients with the most efficient localisation the tumour to body ratio was 20:1 and tumour to blood ratio 5:1. This may be sufficient for effective therapy of cancer in patients selected for efficient antibody localisation. The data may be used to estimate the effect of different therapeutic strategies. For instance, in the time after second antibody administration the average tumour to blood ratio of radiation dose was 11:1, suggesting that two phase systems in which the therapeutic modality is given after a good tumour to normal tissue ratio is obtained may be effective for the majority of patients.</description><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>clinical-oncology-epidemiology</subject><subject>Drug Resistance</subject><subject>Epidemiology</subject><subject>Molecular Medicine</subject><subject>Oncology</subject><issn>0007-0920</issn><issn>1532-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqVj11KxDAUhcOgMNXxzQXcDbQmLUObRxHFBfge0uSOc0tMyk1G6O7NwGzAp8Ph_MAnxLOSnZLD9DIvrlN60l2vjzvRqOPQt2rqxzvRSCnHVupe7sVDzku1Wk5jI-JrLDQnv4GnXJjmS6EUwUYPPmX6wcIbUITVFsJYMjA6pF-K38DWUwp2xhDQ18Xtp5yR7brBKTG4FFIdFBvA2eiQD-L-ZEPGp5s-ivbj_evts80r109ks6QLxxoZJc0VylQoc4UyFWr4b_8PjstX9A</recordid><startdate>19890901</startdate><enddate>19890901</enddate><creator>Begent, RHJ</creator><creator>Ledermann, JA</creator><creator>Green, AJ</creator><creator>Bagshawe, KD</creator><creator>Riggs, SJ</creator><creator>Searle, F</creator><creator>Keep, PA</creator><creator>Adam, T</creator><creator>Dale, RG</creator><creator>Glaser, MG</creator><general>Nature Publishing Group UK</general><scope/></search><sort><creationdate>19890901</creationdate><title>Antibody distribution and dosimetry in patients receiving radiolabelled antibody therapy for colorectal cancer</title><author>Begent, RHJ ; Ledermann, JA ; Green, AJ ; Bagshawe, KD ; Riggs, SJ ; Searle, F ; Keep, PA ; Adam, T ; Dale, RG ; Glaser, MG</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-springer_journals_10_1038_bjc_1989_2953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>clinical-oncology-epidemiology</topic><topic>Drug Resistance</topic><topic>Epidemiology</topic><topic>Molecular Medicine</topic><topic>Oncology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Begent, RHJ</creatorcontrib><creatorcontrib>Ledermann, JA</creatorcontrib><creatorcontrib>Green, AJ</creatorcontrib><creatorcontrib>Bagshawe, KD</creatorcontrib><creatorcontrib>Riggs, SJ</creatorcontrib><creatorcontrib>Searle, F</creatorcontrib><creatorcontrib>Keep, PA</creatorcontrib><creatorcontrib>Adam, T</creatorcontrib><creatorcontrib>Dale, RG</creatorcontrib><creatorcontrib>Glaser, MG</creatorcontrib><jtitle>British journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Begent, RHJ</au><au>Ledermann, JA</au><au>Green, AJ</au><au>Bagshawe, KD</au><au>Riggs, SJ</au><au>Searle, F</au><au>Keep, PA</au><au>Adam, T</au><au>Dale, RG</au><au>Glaser, MG</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antibody distribution and dosimetry in patients receiving radiolabelled antibody therapy for colorectal cancer: Clinical Oncology/Epidemiology</atitle><jtitle>British journal of cancer</jtitle><stitle>Br J Cancer</stitle><date>1989-09-01</date><risdate>1989</risdate><volume>60</volume><issue>3</issue><spage>406</spage><epage>412</epage><pages>406-412</pages><issn>0007-0920</issn><eissn>1532-1827</eissn><abstract>The distribution of iodine-131 (131I) labelled antibody to carcinoembryonic antigen (CEA) has been studied in 16 patients with colorectal cancer. Levels of tumour and normal tissue radioactivity were measured by serial gamma-camera imaging and counting of blood and urine. Maximum concentrations were found in tumour 8 h after administration and varied up to 9-fold in different patients. Higher levels were found on average in tumour than in any other tissue. Liver, lung and blood were the other tissues in which antibody was concentrated relative to the rest of the body. Antibody cleared from all these tissues over 1 week. Second antibody directed against the antitumour (first) antibody was given 24 h after first antibody in order to accelerate clearance from the blood. This increased the tumour to blood ratio but had little effect on other tissues. Cumulative radiation dose to tumour and normal tissue was estimated. In patients with the most efficient localisation the tumour to body ratio was 20:1 and tumour to blood ratio 5:1. This may be sufficient for effective therapy of cancer in patients selected for efficient antibody localisation. The data may be used to estimate the effect of different therapeutic strategies. For instance, in the time after second antibody administration the average tumour to blood ratio of radiation dose was 11:1, suggesting that two phase systems in which the therapeutic modality is given after a good tumour to normal tissue ratio is obtained may be effective for the majority of patients.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><doi>10.1038/bjc.1989.295</doi></addata></record> |
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source | SpringerLink Journals; Nature Journals Online; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | Biomedical and Life Sciences Biomedicine Cancer Research clinical-oncology-epidemiology Drug Resistance Epidemiology Molecular Medicine Oncology |
title | Antibody distribution and dosimetry in patients receiving radiolabelled antibody therapy for colorectal cancer: Clinical Oncology/Epidemiology |
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