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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
1992-12-16
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pubmed:abstractText |
Disease recurrence remains a major limitation to the use of marrow transplantation to treat leukemia. Previous transplant studies have demonstrated that higher doses of total-body irradiation result in less disease recurrence, but more toxicity. In this study, the possibility of delivering radiotherapy specifically to marrow using a radiolabeled anti-CD33 antibody (p67) was explored. Biodistribution studies were performed in nine patients using .05-.5 mg/kg p67 trace-labeled with 131I. In most patients initial specific uptake of 131I-p67 in the marrow was seen, but the half-life of the radiolabel in the marrow space was relatively brief, ranging from 9-41 hr, presumably due to modulation of the 131I-p67-CD33 complex with subsequent digestion and release of 131I from the marrow space. In four of nine patients these biodistribution studies demonstrated that with 131I-p67 marrow and spleen would receive more radiation than any normal nonhematopoietic organ, and therefore these four patients were treated with 110-330 mCi 131I conjugated to p67 followed by a standard transplant regimen of cyclophosphamide plus 12 Gy TBI. All four patients tolerated the procedure well and three of the four are alive in remission 195-477 days posttransplant. This study demonstrates the feasibility of using a radiolabeled antimyeloid antibody as part of a marrow transplant preparative regimen and also highlights a major limitation of using conventionally labeled anti-CD33--namely, the short residence time in marrow. Strategies to overcome this limitation include the use of alternative labeling techniques or the selection of cell surface stable antigens as targets.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Differentiation...,
http://linkedlifedata.com/resource/pubmed/chemical/CD33 antigen,
http://linkedlifedata.com/resource/pubmed/chemical/Iodine Radioisotopes
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0041-1337
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
54
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pubmed:owner |
NLM
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pubmed:authorsComplete |
N
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pubmed:pagination |
829-33
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:1440849-Adolescent,
pubmed-meshheading:1440849-Adult,
pubmed-meshheading:1440849-Antibodies,
pubmed-meshheading:1440849-Antigens, CD,
pubmed-meshheading:1440849-Antigens, Differentiation, Myelomonocytic,
pubmed-meshheading:1440849-Bone Marrow,
pubmed-meshheading:1440849-Bone Marrow Transplantation,
pubmed-meshheading:1440849-Female,
pubmed-meshheading:1440849-Half-Life,
pubmed-meshheading:1440849-Humans,
pubmed-meshheading:1440849-Iodine Radioisotopes,
pubmed-meshheading:1440849-Leukemia, Myeloid, Acute,
pubmed-meshheading:1440849-Male,
pubmed-meshheading:1440849-Middle Aged,
pubmed-meshheading:1440849-Pharmacokinetics,
pubmed-meshheading:1440849-Time Factors
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pubmed:year |
1992
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pubmed:articleTitle |
The use of radiolabeled anti-CD33 antibody to augment marrow irradiation prior to marrow transplantation for acute myelogenous leukemia.
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pubmed:affiliation |
Fred Hutchinson Cancer Research Center, Seattle, WA 98104.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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