Source:http://linkedlifedata.com/resource/pubmed/id/11585290
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2001-10-4
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pubmed:abstractText |
The somatostatin analogue [DOTA0,Tyr3]octreotate has a nine-fold higher affinity for the somatostatin receptor subtype 2 as compared with [DOTA0, Tyr3]octreotide. Also, labelled with the beta- and gamma-emitting radionuclide lutetium-177, this compound has been shown to have a very favourable impact on tumour regression and animal survival in a rat model. Because of these reported advantages over the analogues currently used for somatostatin receptor-mediated radiotherapy, we decided to compare [177Lu-DOTA0,Tyr3]octreotate (177Lu-octreotate) with [111In-DTPA0]octreotide (111In-octreotide) in six patients with somatostatin receptor-positive tumours. Plasma radioactivity after 177Lu-octreotate expressed as a percentage of the injected dose was comparable with that after 111In-octreotide. Urinary excretion of radioactivity was significantly lower than after 111In-octreotide, averaging 64% after 24 h. The uptake after 24 h, expressed as a percentage of the injected dose of 177Lu-octreotate, was comparable to that after 111In-octreotide for kidneys, spleen and liver, but was three- to fourfold higher for four of five tumours. The spleen and kidneys received the highest absorbed doses. The doses to the kidneys were reduced by a mean of 47% after co-infusion of amino acids. It is concluded that in comparison with the radionuclide-coupled somatostatin analogues that are currently available for somatostatin receptor-mediated radiotherapy, 177Lu-octreotate potentially represents an important improvement. Higher absorbed doses can be achieved to most tumours, with about equal doses to potentially dose-limiting organs; furthermore, the lower tissue penetration range of 177Lu as compared with 90Y may be especially important for small tumours.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Indium Radioisotopes,
http://linkedlifedata.com/resource/pubmed/chemical/Lutetium,
http://linkedlifedata.com/resource/pubmed/chemical/Octreotide,
http://linkedlifedata.com/resource/pubmed/chemical/Organometallic Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Radioisotopes,
http://linkedlifedata.com/resource/pubmed/chemical/Radiopharmaceuticals,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Somatostatin,
http://linkedlifedata.com/resource/pubmed/chemical/Somatostatin,
http://linkedlifedata.com/resource/pubmed/chemical/pentetreotide
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0340-6997
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
28
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1319-25
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:11585290-Adolescent,
pubmed-meshheading:11585290-Adult,
pubmed-meshheading:11585290-Aged,
pubmed-meshheading:11585290-Female,
pubmed-meshheading:11585290-Humans,
pubmed-meshheading:11585290-Indium Radioisotopes,
pubmed-meshheading:11585290-Lutetium,
pubmed-meshheading:11585290-Male,
pubmed-meshheading:11585290-Middle Aged,
pubmed-meshheading:11585290-Neoplasms,
pubmed-meshheading:11585290-Octreotide,
pubmed-meshheading:11585290-Organometallic Compounds,
pubmed-meshheading:11585290-Radiation Dosage,
pubmed-meshheading:11585290-Radioisotopes,
pubmed-meshheading:11585290-Radiopharmaceuticals,
pubmed-meshheading:11585290-Receptors, Somatostatin,
pubmed-meshheading:11585290-Somatostatin
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pubmed:year |
2001
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pubmed:articleTitle |
[177Lu-DOTAOTyr3]octreotate: comparison with [111In-DTPAo]octreotide in patients.
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pubmed:affiliation |
Department of Nuclear Medicine, University Hospital Rotterdam, The Netherlands. djkwekkeboom@hotmail.com
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pubmed:publicationType |
Journal Article,
Comparative Study
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