Source:http://linkedlifedata.com/resource/pubmed/id/10088162
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1999-6-24
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pubmed:abstractText |
In this study, we evaluated the efficacy of bone marrow immunoscintigraphy (BMIS) for the detection of skeletal metastases in 23 patients with histologically confirmed breast cancer. All patients underwent whole-body BMIS 3-6 h after the intravenous injection of 0.20-0.33 mg of the intact anti-NCA 95 MAb BW 250/183 labelled with 259-555 MBq 99Tcm and a whole-body 99Tcm-MDP bone scan. In four patients, BMIS SPET of the lumbar spine was also performed. Serum alkaline phosphatase was determined in all patients and the level of human anti-mouse antibody (HAMA) in 16. Final diagnosis was confirmed by radiology and 2 years follow-up. Compared with the 99Tcm-MDP bone scan, BMIS demonstrated better specificity (88% vs 75%) and a better positive predictive value (92% vs 85%). There were no significant differences between BMIS and the bone scan in the detection of skeletal metastases (P > 0.05). In one patient with normal planar BMIS of the lumbar spine, SPET disclosed a metastatic lesion in the bone marrow. The correlation coefficient between BMIS and bone scan and between BMIS and serum alkaline phosphatase was r = 0.688 and r = 0.483 respectively. One patient developed a minor HAMA response after BMIS. Patients with diffuse increased activity of the skull on the bone scan had a significantly higher skull to whole body ratio on BMIS (P < 0.01). Thus BMIS can improve the specificity and positive predictive value of bone scanning in the detection of skeletal metastases, with a low HAMA response. Diffuse increased activity of the skull on bone scans could be explained by bone marrow extension. SPET scanning of the spine may improve the sensitivity of BMIS.
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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/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Neoplasm,
http://linkedlifedata.com/resource/pubmed/chemical/BW 250 183,
http://linkedlifedata.com/resource/pubmed/chemical/Cell Adhesion Molecules,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Radiopharmaceuticals,
http://linkedlifedata.com/resource/pubmed/chemical/Technetium Tc 99m Medronate
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0143-3636
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
135-43
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10088162-Adult,
pubmed-meshheading:10088162-Aged,
pubmed-meshheading:10088162-Antibodies, Monoclonal,
pubmed-meshheading:10088162-Antigens, Neoplasm,
pubmed-meshheading:10088162-Bone Marrow,
pubmed-meshheading:10088162-Bone Marrow Neoplasms,
pubmed-meshheading:10088162-Bone Neoplasms,
pubmed-meshheading:10088162-Breast Neoplasms,
pubmed-meshheading:10088162-Cell Adhesion Molecules,
pubmed-meshheading:10088162-Female,
pubmed-meshheading:10088162-Humans,
pubmed-meshheading:10088162-Lumbosacral Region,
pubmed-meshheading:10088162-Membrane Glycoproteins,
pubmed-meshheading:10088162-Middle Aged,
pubmed-meshheading:10088162-Radioimmunodetection,
pubmed-meshheading:10088162-Radiopharmaceuticals,
pubmed-meshheading:10088162-Sensitivity and Specificity,
pubmed-meshheading:10088162-Technetium Tc 99m Medronate,
pubmed-meshheading:10088162-Tomography, Emission-Computed,
pubmed-meshheading:10088162-Whole-Body Counting
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pubmed:year |
1999
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pubmed:articleTitle |
Bone marrow immunoscintigraphy for the detection of skeletal metastases in patients with breast cancer.
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pubmed:affiliation |
Department of Oncology and Nuclear Medicine, University Hospital Sestre Milosrdnice, Zagreb, Croatia. MiodragLacic@public.srce.hr
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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