Source:http://linkedlifedata.com/resource/pubmed/id/15100153
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2004-7-21
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pubmed:abstractText |
We report a phase 1 study of pharmacokinetics, dosimetry, toxicity, and response of (131)I anti-tenascin chimeric 81C6 for the treatment of lymphoma. Nine patients received a dosimetric dose of 370 MBq (10 mCi). Three patients received an administered activity of 1480 MBq (40 mCi), and 2 developed hematologic toxicity that required stem cell infusion. Six patients received an administered activity of 1110 MBq (30 mCi), and 2 developed toxicity that required stem cell infusion. The clearance of whole-body activity was monoexponential with a mean effective half-life of 110 hours (range, 90-136 hours) and a mean effective whole-body residence time of 159 hours (range, 130-196 hours). There was rapid uptake within the viscera; however, tumor uptake was slower. Activity in normal viscera decreased proportional to the whole body; however, tumor sites presented a slow clearance (T(1/2), 86-191 hours). The mean absorbed dose to whole-body was 67 cGy (range, 51-89 hours), whereas the dose to tumor sites was 963 cGy (range, 363-1517 cGy). Despite lack of a "blocking" antibody, 1 of 9 patients attained a complete remission and 1 a partial remission. These data demonstrate this radiopharmaceutical to be an encouraging agent for the treatment of lymphoma particularly if methods to protect the normal viscera are developed.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0006-4971
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pubmed:author |
pubmed-author:AkabaniGamalG,
pubmed-author:AndersonElizabethE,
pubmed-author:BignerDarell DDD,
pubmed-author:BowsherJames EJE,
pubmed-author:ChaoNelson JNJ,
pubmed-author:ClaytonSteveS,
pubmed-author:ColemanR EdwardRE,
pubmed-author:DeCastroCarlosC,
pubmed-author:GasparettoCristinaC,
pubmed-author:GockermanJon PJP,
pubmed-author:LagooAnandA,
pubmed-author:MetzlerScott DSD,
pubmed-author:MooreJoseph OJO,
pubmed-author:PegramCharles NCN,
pubmed-author:RizzieriDavid ADA,
pubmed-author:ToasoBonnieB,
pubmed-author:ZalutskyMichael RMR
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pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
104
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
642-8
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:15100153-Animals,
pubmed-meshheading:15100153-Antibodies, Monoclonal,
pubmed-meshheading:15100153-Biological Transport,
pubmed-meshheading:15100153-Biopsy,
pubmed-meshheading:15100153-Bone Marrow,
pubmed-meshheading:15100153-Female,
pubmed-meshheading:15100153-Humans,
pubmed-meshheading:15100153-Immunotoxins,
pubmed-meshheading:15100153-Iodine Radioisotopes,
pubmed-meshheading:15100153-Lymph Nodes,
pubmed-meshheading:15100153-Lymphoma, Non-Hodgkin,
pubmed-meshheading:15100153-Male,
pubmed-meshheading:15100153-Mice,
pubmed-meshheading:15100153-Patient Selection,
pubmed-meshheading:15100153-Tenascin,
pubmed-meshheading:15100153-Tissue Distribution,
pubmed-meshheading:15100153-Tomography, X-Ray Computed
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pubmed:year |
2004
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pubmed:articleTitle |
Phase 1 trial study of 131I-labeled chimeric 81C6 monoclonal antibody for the treatment of patients with non-Hodgkin lymphoma.
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pubmed:affiliation |
Department of Medicine, Duke University Medical Center, Durham, NC 27710, USA. rizzi003@mc.duke.edu
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't,
Clinical Trial, Phase I
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