Source:http://linkedlifedata.com/resource/pubmed/id/11418314
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-2
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pubmed:dateCreated |
2001-6-21
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pubmed:abstractText |
We have recently reported that a radioiodinated, DTPA-appended peptide, designated IMP-R1, is a residualizing iodine label that overcomes many of the limitations that have impeded the development of residualizing iodine for clinical use. In this study the potential of 131I-IMP-R1-RS7, an internalizing anti-EGP-1 monoclonal antibody, was evaluated by performing preclinical therapy studies in nude mice bearing Calu-3 human non-small cell carcinoma of the lung xenografis. Elimination of 6 of 9 established tumors (mean tumor volume=0.3 cm(3)) was observed using a single dose of 350 microCi/mouse of 131I-IMP-R1-RS7, with all animals tolerating the dose. At the same dose and specific activity of 131I-RS7, labeled using the conventional chloramine-T method, there were four deaths, and one complete remission in nine treated mice. At the maximum tolerated dose of conventionally 131I-labeled RS7, 275 microCi, mean stable disease for approximately 5 weeks was observed, with no complete responses. Specificity of the therapeutic effect was shown in an isotype-matched control experiment, where 131I-IMP-R1-RS7 was markedly more effective than the (131)I-IMP-R1-labeled control antibody. These studies demonstrate that (131)I-IMP-R1-RS7 provides a therapeutic advantage in comparison to conventional 131I-labeled RS7, as predicted by the increased tumor accretion observed previously in targeting studies. A direct comparison of the maximum tolerated doses of (131)I-IMP-R1-RS7 (350 microCi) and 90Y-DOTA-RS7 (105 microCi) was performed in this tumor model using large established tumors (mean tumor volume=0.85 cm(3)). Anti-tumor efficacy and toxicity of the two treatments were comparable.
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pubmed:grant | |
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:issn |
1040-8428
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
39
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
173-80
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:11418314-Animals,
pubmed-meshheading:11418314-Antibodies, Monoclonal,
pubmed-meshheading:11418314-Carcinoma, Non-Small-Cell Lung,
pubmed-meshheading:11418314-Dose-Response Relationship, Radiation,
pubmed-meshheading:11418314-Drug Evaluation, Preclinical,
pubmed-meshheading:11418314-Humans,
pubmed-meshheading:11418314-Iodine Radioisotopes,
pubmed-meshheading:11418314-Lung Neoplasms,
pubmed-meshheading:11418314-Membrane Proteins,
pubmed-meshheading:11418314-Mice,
pubmed-meshheading:11418314-Mice, Nude,
pubmed-meshheading:11418314-Neoplasm Transplantation,
pubmed-meshheading:11418314-Radioimmunotherapy,
pubmed-meshheading:11418314-Transplantation, Heterologous,
pubmed-meshheading:11418314-Treatment Outcome
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pubmed:articleTitle |
Successful therapy of a human lung cancer xenograft using MAb RS7 labeled with residualizing radioiodine.
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pubmed:affiliation |
Garden State Cancer Center, 520 Belleville Avenue, Belleville, NJ 07109, USA. rstein.gscancer@att.net
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.
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