Source:http://linkedlifedata.com/resource/pubmed/id/19653815
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2010-5-24
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pubmed:abstractText |
Bone metastases place patients at increased risk of skeletal-related events (SREs), including pathologic fractures, spinal cord compression, severe pain requiring radiotherapy or surgery, and hypercalcemia, because of increased osteoclast-mediated bone resorption. Denosumab, a fully human monoclonal antibody, decreases bone resorption by inhibiting RANKL, which mediates osteoclast activity. We compared the effects of denosumab in two phase 2 studies in patients with bone metastases naive to intravenous bisphosphonate therapy (IV BP; n = 255) and those with elevated levels of the bone resorption marker urinary N-telopeptide (uNTX) despite ongoing IV BP treatment (n = 111). Patients were randomized to receive IV BP every 4 weeks or subcutaneous denosumab every 4 weeks (30/120/180 mg) or every 12 weeks (60/180 mg). Patients treated with denosumab experienced a rapid and sustained reduction in bone turnover regardless of prior IV BP exposure. After 25 weeks, the median uNTX reduction was 75% (IV BP-naive) and 80% (prior IV BP) after denosumab treatment and 71% (IV BP-naive) and 56% (prior IV BP) in the IV BP arms. Denosumab patients with prior IV BP exposure had marked suppression of the osteoclast marker TRAP-5b (median reduction: denosumab 73%, IV BP 11%). SRE incidence was low across both studies. In patients previously treated with BPs, the rate of first on-study SRE was lower in the denosumab groups (8%) than the IV BP group (17%). Denosumab appeared to be well tolerated in both studies. Denosumab suppresses bone resorption markers independently of prior BP treatment, even in patients who appear to respond poorly to BPs.
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pubmed:commentsCorrections | |
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/Biological Markers,
http://linkedlifedata.com/resource/pubmed/chemical/Bone Density Conservation Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Diphosphonates,
http://linkedlifedata.com/resource/pubmed/chemical/RANK Ligand,
http://linkedlifedata.com/resource/pubmed/chemical/denosumab
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1523-4681
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2010 American Society for Bone and Mineral Research.
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pubmed:issnType |
Electronic
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pubmed:volume |
25
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
440-6
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pubmed:meshHeading |
pubmed-meshheading:19653815-Antibodies, Monoclonal,
pubmed-meshheading:19653815-Biological Markers,
pubmed-meshheading:19653815-Bone Density Conservation Agents,
pubmed-meshheading:19653815-Bone Neoplasms,
pubmed-meshheading:19653815-Bone and Bones,
pubmed-meshheading:19653815-Diphosphonates,
pubmed-meshheading:19653815-Female,
pubmed-meshheading:19653815-Humans,
pubmed-meshheading:19653815-Injections, Subcutaneous,
pubmed-meshheading:19653815-Male,
pubmed-meshheading:19653815-Middle Aged,
pubmed-meshheading:19653815-Neoplasms,
pubmed-meshheading:19653815-RANK Ligand
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pubmed:year |
2010
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pubmed:articleTitle |
Effects of denosumab in patients with bone metastases with and without previous bisphosphonate exposure.
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pubmed:affiliation |
CHU Brugmann, Université Libre de Bruxelles, Brussels, Belgium. Jean-jacques.body@chu-brugmann.be
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pubmed:publicationType |
Journal Article,
Randomized Controlled Trial,
Research Support, Non-U.S. Gov't,
Multicenter Study,
Clinical Trial, Phase II
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