Complete Tumor Ablation With Iodine 131-Radiolabeled Disialoganglioside GD2-Specific Monoclonal Antibody Against Human Neuroblastoma Xenografted in Nude Mice
The antibody 3F8, an IgG3 murine monoclonal antibody (MoAb) against disialoganglioside GD2, could target iodine-131 (131I) to established subcutaneous human neuroblastoma (NB) xenografts in BALB/c nude mice. 131l-radiolabeled MoAb (0.125–1 mCi) was injected iv. Tumor radioactivity over time was calc...
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Veröffentlicht in: | JNCI : Journal of the National Cancer Institute 1986-09, Vol.77 (3), p.739-745 |
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creator | Cheung, Nai-Kong V. Landmeier, Bonnie Neely, John Nelson, A. Dennis Abramowsky, Carlos Ellery, Susan Adams, Robert B. Miraldi, Floro |
description | The antibody 3F8, an IgG3 murine monoclonal antibody (MoAb) against disialoganglioside GD2, could target iodine-131 (131I) to established subcutaneous human neuroblastoma (NB) xenografts in BALB/c nude mice. 131l-radiolabeled MoAb (0.125–1 mCi) was injected iv. Tumor radioactivity over time was calculated from scintigraphy, and radiation dose to individual tumors was calculated. Tumor shrinkage occurred only with 131I-labeled 3F8, but not with nonradioactive 3F8 or radiolabeled irrelevant antibody. While the tumor of the control mice enlarged by tenfold, the treated tumor showed over 95% shrinkage by 12 days. Both the rate of shrinkage and duration of tumor response were dose dependent. Calculated doses of more than 10,000 rad could be achieved. Only those tumors that received more than 4,200 rad were completely ablated without recurrence. Recurrent tumors were not antigen negative or radioresistant. These results confirmed the prediction based on imaging studies that human NB xenografts could be effectively eradicated with the use of 131I-labeled MoAb 3F8 with tolerable toxicities. |
doi_str_mv | 10.1093/jnci/77.3.739 |
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Dennis ; Abramowsky, Carlos ; Ellery, Susan ; Adams, Robert B. ; Miraldi, Floro</creator><creatorcontrib>Cheung, Nai-Kong V. ; Landmeier, Bonnie ; Neely, John ; Nelson, A. Dennis ; Abramowsky, Carlos ; Ellery, Susan ; Adams, Robert B. ; Miraldi, Floro</creatorcontrib><description>The antibody 3F8, an IgG3 murine monoclonal antibody (MoAb) against disialoganglioside GD2, could target iodine-131 (131I) to established subcutaneous human neuroblastoma (NB) xenografts in BALB/c nude mice. 131l-radiolabeled MoAb (0.125–1 mCi) was injected iv. Tumor radioactivity over time was calculated from scintigraphy, and radiation dose to individual tumors was calculated. Tumor shrinkage occurred only with 131I-labeled 3F8, but not with nonradioactive 3F8 or radiolabeled irrelevant antibody. While the tumor of the control mice enlarged by tenfold, the treated tumor showed over 95% shrinkage by 12 days. Both the rate of shrinkage and duration of tumor response were dose dependent. Calculated doses of more than 10,000 rad could be achieved. Only those tumors that received more than 4,200 rad were completely ablated without recurrence. Recurrent tumors were not antigen negative or radioresistant. These results confirmed the prediction based on imaging studies that human NB xenografts could be effectively eradicated with the use of 131I-labeled MoAb 3F8 with tolerable toxicities.</description><identifier>ISSN: 0027-8874</identifier><identifier>EISSN: 1460-2105</identifier><identifier>DOI: 10.1093/jnci/77.3.739</identifier><identifier>PMID: 3091900</identifier><language>eng</language><publisher>Cary, NC: Oxford University Press</publisher><subject>Animal tumors. Experimental tumors ; Animals ; Antibodies, Monoclonal - therapeutic use ; Biological and medical sciences ; Dose-Response Relationship, Radiation ; Experimental nervous system tumors ; Female ; Gangliosides - immunology ; Humans ; Iodine Radioisotopes - therapeutic use ; Iodine Radioisotopes - toxicity ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Mice, Nude ; Neoplasm Transplantation ; Neuroblastoma - pathology ; Neuroblastoma - radiotherapy ; Transplantation, Heterologous ; Tumors</subject><ispartof>JNCI : Journal of the National Cancer Institute, 1986-09, Vol.77 (3), p.739-745</ispartof><rights>1987 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8079751$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3091900$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cheung, Nai-Kong V.</creatorcontrib><creatorcontrib>Landmeier, Bonnie</creatorcontrib><creatorcontrib>Neely, John</creatorcontrib><creatorcontrib>Nelson, A. Dennis</creatorcontrib><creatorcontrib>Abramowsky, Carlos</creatorcontrib><creatorcontrib>Ellery, Susan</creatorcontrib><creatorcontrib>Adams, Robert B.</creatorcontrib><creatorcontrib>Miraldi, Floro</creatorcontrib><title>Complete Tumor Ablation With Iodine 131-Radiolabeled Disialoganglioside GD2-Specific Monoclonal Antibody Against Human Neuroblastoma Xenografted in Nude Mice</title><title>JNCI : Journal of the National Cancer Institute</title><addtitle>Journal of the National Cancer Institute</addtitle><description>The antibody 3F8, an IgG3 murine monoclonal antibody (MoAb) against disialoganglioside GD2, could target iodine-131 (131I) to established subcutaneous human neuroblastoma (NB) xenografts in BALB/c nude mice. 131l-radiolabeled MoAb (0.125–1 mCi) was injected iv. Tumor radioactivity over time was calculated from scintigraphy, and radiation dose to individual tumors was calculated. Tumor shrinkage occurred only with 131I-labeled 3F8, but not with nonradioactive 3F8 or radiolabeled irrelevant antibody. While the tumor of the control mice enlarged by tenfold, the treated tumor showed over 95% shrinkage by 12 days. Both the rate of shrinkage and duration of tumor response were dose dependent. Calculated doses of more than 10,000 rad could be achieved. Only those tumors that received more than 4,200 rad were completely ablated without recurrence. Recurrent tumors were not antigen negative or radioresistant. These results confirmed the prediction based on imaging studies that human NB xenografts could be effectively eradicated with the use of 131I-labeled MoAb 3F8 with tolerable toxicities.</description><subject>Animal tumors. Experimental tumors</subject><subject>Animals</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Dose-Response Relationship, Radiation</subject><subject>Experimental nervous system tumors</subject><subject>Female</subject><subject>Gangliosides - immunology</subject><subject>Humans</subject><subject>Iodine Radioisotopes - therapeutic use</subject><subject>Iodine Radioisotopes - toxicity</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Nude</subject><subject>Neoplasm Transplantation</subject><subject>Neuroblastoma - pathology</subject><subject>Neuroblastoma - radiotherapy</subject><subject>Transplantation, Heterologous</subject><subject>Tumors</subject><issn>0027-8874</issn><issn>1460-2105</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE2P0zAURS0EGsrAkiWSF2zTef5IHC-rlrYjdQYJihixiV4Sp3hw7Cp2JObH8F-xNNW8zV2co_ukS8hHBksGWtw8-s7eKLUUSyX0K7JgsoKCMyhfkwUAV0VdK_mWvIvxEfJpLq_IlQDNNMCC_FuH8exMMvQ4j2Giq9ZhssHTnzb9preht95QJljxDXsbHLbGmZ5ubLTowgn9ydkQbW_obsOL72fT2cF29C740Lng0dGVT7YN_RNdndD6mOh-HtHTezNPIf-KKYxIH4wPpwmHlLtthnMuvLOdeU_eDOii-XDJa_Jj--W43heHr7vb9epQWFbXqcBWc6U5ly3rQIE0cgDeVwMHWVbQlsBZpdoKWIUd8hL5ALKtQQrZDzpTcU0-Pfee53Y0fXOe7IjTU3OZKfPPF46xQzdMmEePL1oNSquSZa141mxM5u8LxulPUymhymb_8Ks5HLe7zVbr5l78B7FzhlE</recordid><startdate>198609</startdate><enddate>198609</enddate><creator>Cheung, Nai-Kong V.</creator><creator>Landmeier, Bonnie</creator><creator>Neely, John</creator><creator>Nelson, A. Dennis</creator><creator>Abramowsky, Carlos</creator><creator>Ellery, Susan</creator><creator>Adams, Robert B.</creator><creator>Miraldi, Floro</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>198609</creationdate><title>Complete Tumor Ablation With Iodine 131-Radiolabeled Disialoganglioside GD2-Specific Monoclonal Antibody Against Human Neuroblastoma Xenografted in Nude Mice</title><author>Cheung, Nai-Kong V. ; Landmeier, Bonnie ; Neely, John ; Nelson, A. Dennis ; Abramowsky, Carlos ; Ellery, Susan ; Adams, Robert B. ; Miraldi, Floro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i188t-ab9279224b1c0704e4f02d6f204560b502167b6016aca25a2f04b80434df95023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Animal tumors. Experimental tumors</topic><topic>Animals</topic><topic>Antibodies, Monoclonal - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Dose-Response Relationship, Radiation</topic><topic>Experimental nervous system tumors</topic><topic>Female</topic><topic>Gangliosides - immunology</topic><topic>Humans</topic><topic>Iodine Radioisotopes - therapeutic use</topic><topic>Iodine Radioisotopes - toxicity</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Nude</topic><topic>Neoplasm Transplantation</topic><topic>Neuroblastoma - pathology</topic><topic>Neuroblastoma - radiotherapy</topic><topic>Transplantation, Heterologous</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cheung, Nai-Kong V.</creatorcontrib><creatorcontrib>Landmeier, Bonnie</creatorcontrib><creatorcontrib>Neely, John</creatorcontrib><creatorcontrib>Nelson, A. Dennis</creatorcontrib><creatorcontrib>Abramowsky, Carlos</creatorcontrib><creatorcontrib>Ellery, Susan</creatorcontrib><creatorcontrib>Adams, Robert B.</creatorcontrib><creatorcontrib>Miraldi, Floro</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>JNCI : Journal of the National Cancer Institute</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cheung, Nai-Kong V.</au><au>Landmeier, Bonnie</au><au>Neely, John</au><au>Nelson, A. Dennis</au><au>Abramowsky, Carlos</au><au>Ellery, Susan</au><au>Adams, Robert B.</au><au>Miraldi, Floro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Complete Tumor Ablation With Iodine 131-Radiolabeled Disialoganglioside GD2-Specific Monoclonal Antibody Against Human Neuroblastoma Xenografted in Nude Mice</atitle><jtitle>JNCI : Journal of the National Cancer Institute</jtitle><addtitle>Journal of the National Cancer Institute</addtitle><date>1986-09</date><risdate>1986</risdate><volume>77</volume><issue>3</issue><spage>739</spage><epage>745</epage><pages>739-745</pages><issn>0027-8874</issn><eissn>1460-2105</eissn><abstract>The antibody 3F8, an IgG3 murine monoclonal antibody (MoAb) against disialoganglioside GD2, could target iodine-131 (131I) to established subcutaneous human neuroblastoma (NB) xenografts in BALB/c nude mice. 131l-radiolabeled MoAb (0.125–1 mCi) was injected iv. Tumor radioactivity over time was calculated from scintigraphy, and radiation dose to individual tumors was calculated. Tumor shrinkage occurred only with 131I-labeled 3F8, but not with nonradioactive 3F8 or radiolabeled irrelevant antibody. While the tumor of the control mice enlarged by tenfold, the treated tumor showed over 95% shrinkage by 12 days. Both the rate of shrinkage and duration of tumor response were dose dependent. Calculated doses of more than 10,000 rad could be achieved. Only those tumors that received more than 4,200 rad were completely ablated without recurrence. Recurrent tumors were not antigen negative or radioresistant. These results confirmed the prediction based on imaging studies that human NB xenografts could be effectively eradicated with the use of 131I-labeled MoAb 3F8 with tolerable toxicities.</abstract><cop>Cary, NC</cop><pub>Oxford University Press</pub><pmid>3091900</pmid><doi>10.1093/jnci/77.3.739</doi><tpages>7</tpages></addata></record> |
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subjects | Animal tumors. Experimental tumors Animals Antibodies, Monoclonal - therapeutic use Biological and medical sciences Dose-Response Relationship, Radiation Experimental nervous system tumors Female Gangliosides - immunology Humans Iodine Radioisotopes - therapeutic use Iodine Radioisotopes - toxicity Medical sciences Mice Mice, Inbred BALB C Mice, Nude Neoplasm Transplantation Neuroblastoma - pathology Neuroblastoma - radiotherapy Transplantation, Heterologous Tumors |
title | Complete Tumor Ablation With Iodine 131-Radiolabeled Disialoganglioside GD2-Specific Monoclonal Antibody Against Human Neuroblastoma Xenografted in Nude Mice |
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