Source:http://linkedlifedata.com/resource/pubmed/id/18165618
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
|
pubmed:dateCreated |
2007-12-31
|
pubmed:abstractText |
There is a misconception that elderly cancer patients cannot tolerate standard doses of chemotherapy because of the frequency and severity of myelosuppressive complications. The reactive use of colony-stimulating factors (i.e., in response to severe neutropenia) commonly observed in this setting contributes to the frequency and severity of these complications. This study evaluated the incidence of febrile neutropenia and related events in elderly cancer patients receiving pegfilgrastim beginning with cycle 1 (proactive) in comparison with pegfilgrastim initiated after cycle 1 at the physician's discretion (reactive).
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
1083-7159
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
12
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1416-24
|
pubmed:dateRevised |
2011-11-17
|
pubmed:meshHeading |
pubmed-meshheading:18165618-Aged,
pubmed-meshheading:18165618-Aged, 80 and over,
pubmed-meshheading:18165618-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:18165618-Drug Toxicity,
pubmed-meshheading:18165618-Female,
pubmed-meshheading:18165618-Granulocyte Colony-Stimulating Factor,
pubmed-meshheading:18165618-Humans,
pubmed-meshheading:18165618-Male,
pubmed-meshheading:18165618-Neoplasms,
pubmed-meshheading:18165618-Neutropenia,
pubmed-meshheading:18165618-Recombinant Proteins
|
pubmed:year |
2007
|
pubmed:articleTitle |
Elderly cancer patients receiving chemotherapy benefit from first-cycle pegfilgrastim.
|
pubmed:affiliation |
H Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33612, USA. Balducci@moffitt.usf.edu
|
pubmed:publicationType |
Journal Article,
Randomized Controlled Trial,
Multicenter Study,
Clinical Trial, Phase IV
|