Source:http://linkedlifedata.com/resource/pubmed/id/10541365
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10 Suppl
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pubmed:dateCreated |
1999-11-24
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pubmed:abstractText |
The purpose of this study was 2-fold: to determine the maximum tolerated dose (MTD) of 64Cu-bromoacetamidobenzyl- 1,4,8,11-tetraazacyclotetradecane-N,N',N'',N'''-tetraacetic acid (BAT)-2-iminothiolane (2IT)-monoclonal antibody (MAb) 1A3 in hamsters, and second, to determine the therapeutic efficacy of 64Cu-BAT-2IT-MAb 1A3 at various dose levels in hamsters with large (600 mg), 7-day-old GW39 human colorectal carcinoma tumors. In the MTD studies, non-tumor-bearing hamsters were injected with varying amounts of Cu-64-BAT-2IT MAb 1A3 (>10 mCi) normalized to mCi injected/kg of hamster body weight. Results indicated that the MTD was 150 mCi of Cu-64/kg of body weight. Hamsters receiving higher doses (170-190 mCi/kg) lost greater than 20% of their body weight, and all died between 8 and 13 days (n = 3). All hamsters receiving doses < or = 150 mCi/kg (120-150 mCi; n = 13) survived to the experimental end point (6 weeks) with an overall gain in weight. WBC and platelet counts were depressed in all animals 7 days after treatment but returned to normal values in the survivors by 2 weeks. For larger tumor therapy studies, 40% (8 of 20) of hamsters receiving a single dose of 7.0 mCi and 62.5% (5 of 8) of hamsters receiving 15 mCi of Cu-64-BAT-2IT-MAb 1A3 remained tumor free 4 months after treatment. In dose fractionation studies, hamsters received two 3.5 mCi doses separated by 24 or 48 h with 44% (4 of 9) and 25% (2 of 8) survival, respectively. In every large tumor experimental group, 100% of animals experienced tumor growth inhibition compared to saline control animals. Together, the MTD and the large tumor therapy studies confirm that 64Cu-labeled agents are excellent candidates for radioimmunotherapy trials.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1078-0432
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
5
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3207s-3212s
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10541365-Animals,
pubmed-meshheading:10541365-Antibodies, Monoclonal,
pubmed-meshheading:10541365-Colonic Neoplasms,
pubmed-meshheading:10541365-Copper Radioisotopes,
pubmed-meshheading:10541365-Cricetinae,
pubmed-meshheading:10541365-Humans,
pubmed-meshheading:10541365-Male,
pubmed-meshheading:10541365-Mesocricetus,
pubmed-meshheading:10541365-Mice,
pubmed-meshheading:10541365-Neoplasm Transplantation,
pubmed-meshheading:10541365-Radioimmunotherapy,
pubmed-meshheading:10541365-Radiotherapy Dosage,
pubmed-meshheading:10541365-Transplantation, Heterologous
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pubmed:year |
1999
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pubmed:articleTitle |
Maximum tolerated dose and large tumor radioimmunotherapy studies of 64Cu-labeled monoclonal antibody 1A3 in a colon cancer model.
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pubmed:affiliation |
Department of Surgery, Washington University School of Medicine, St. Louis, Missouri 63110, USA. Connettj@msnotes.wustl.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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