Source:http://linkedlifedata.com/resource/pubmed/id/12026045
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
|
pubmed:dateCreated |
2002-5-23
|
pubmed:abstractText |
Anorexia is a common problem in advanced cancer. Low-dose megestrol acetate, a semi-synthetic progesterone, given twice daily, is an effective appetite stimulant in advanced cancer patients. There was an excellent correlation between patient satisfaction and the primary response criteria (appetite improvement). Given cost, side-effect profile, ease of administration, and efficacy, 80 mg twice daily after meals is an appropriate starting dose of megestrol acetate for anorexia in advanced cancer. If this is not effective, considerable dose escalation is possible.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
N
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:issn |
1049-9091
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
19
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
206-10
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:12026045-Adult,
pubmed-meshheading:12026045-Aged,
pubmed-meshheading:12026045-Aged, 80 and over,
pubmed-meshheading:12026045-Anorexia,
pubmed-meshheading:12026045-Appetite Stimulants,
pubmed-meshheading:12026045-Drug Administration Schedule,
pubmed-meshheading:12026045-Female,
pubmed-meshheading:12026045-Humans,
pubmed-meshheading:12026045-Male,
pubmed-meshheading:12026045-Megestrol Acetate,
pubmed-meshheading:12026045-Middle Aged,
pubmed-meshheading:12026045-Neoplasms,
pubmed-meshheading:12026045-Patient Satisfaction,
pubmed-meshheading:12026045-Questionnaires,
pubmed-meshheading:12026045-Treatment Outcome
|
pubmed:articleTitle |
A phase II study of low-dose megestrol acetate using twice-daily dosing for anorexia in nonhormonally dependent cancer.
|
pubmed:affiliation |
Taussig Cancer Center, Cleveland Clinic Foundation, Ohio, USA.
|
pubmed:publicationType |
Journal Article,
Clinical Trial,
Clinical Trial, Phase II
|