Source:http://linkedlifedata.com/resource/pubmed/id/16585018
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
2006-4-4
|
pubmed:abstractText |
In vitro statins induce apoptosis in myeloma and lymphoma cells in a dose-and time-dependent way. In combination with dexamethasone and doxorubicin, statins have a chemo-sensitizing effect. Twenty-eight patients with relapsed myeloma or lymphoma were treated with a dose-escalating regimen of simvastatin for 7 days followed by VAD in myeloma patients and CHOP in lymphoma patients. The maximum tolerated dose was 15 mg/kg/day simvastatin. The most frequently reported side-effects were fatigue, gastrointestinal CTC grade 1-2 and neutropenic fever. The dose-limiting toxicity was neutropenic sepsis and grade 3 gastrointestinal side effects. High-dose simvastatin given immediately prior to chemotherapy is safe and tolerable up to a dose of 15 mg/kg/day.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
1592-8721
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:volume |
91
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
542-5
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:16585018-Aged,
pubmed-meshheading:16585018-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:16585018-Humans,
pubmed-meshheading:16585018-Lymphoma,
pubmed-meshheading:16585018-Maximum Tolerated Dose,
pubmed-meshheading:16585018-Multiple Myeloma,
pubmed-meshheading:16585018-Recurrence,
pubmed-meshheading:16585018-Salvage Therapy,
pubmed-meshheading:16585018-Simvastatin,
pubmed-meshheading:16585018-Treatment Outcome
|
pubmed:year |
2006
|
pubmed:articleTitle |
Dose-finding study of high-dose simvastatin combined with standard chemotherapy in patients with relapsed or refractory myeloma or lymphoma.
|
pubmed:affiliation |
Department of Hematology and Immunology, University Medical Centre Utrecht, Utrecht, The Netherlands.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Clinical Trial, Phase I
|