Source:http://linkedlifedata.com/resource/pubmed/id/12353818
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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
2002-9-30
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pubmed:abstractText |
Aromatase inhibitors (AIs) are a class of compounds that inhibit the cytochrome P450 aromatase enzyme that mediates conversion of androgens to estrogen in the adrenal gland. AIs have been approved for second-line and, more recently, first-line treatment of advanced breast cancer in postmenopausal women. The most recent, third generation of AIs are the non-steroidal agents anastrozole ('Arimidex') and letrozole, and the steroidal compound exemestane. As second-line therapy, anastrozole demonstrated a significant survival advantage over megestrol acetate (26.7 months v.s. 22.5 months; p < 0.025). Exemestane also produced better survival than megestrol acetate, although these data were less mature. Letrozole 2.5 mg has not demonstrated a survival advantage versus megestrol acetate in the second-line setting. As first-line therapy, anastrozole has demonstrated significant superiority in response rates with respect to time to progression (TTP) (11.1 months v.s. 5.6 months; p = 0.005) and has also demonstrated significantly greater clinical benefit rates compared with tamoxifen (59.1% v.s. 45.6%; p = 0.0098). Letrozole has also demonstrated significantly longer TTP than tamoxifen in the first-line setting (9.5 months v.s. 6 months; p = 0.0001). Important differences between the pharmacological profiles of these agents have been noted, particularly with respect to their effects on glucocorticoid metabolism; data for individual agents should not be extrapolated from one to another, particularly in the adjuvant setting.
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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/Androstadienes,
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Aromatase Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Nitriles,
http://linkedlifedata.com/resource/pubmed/chemical/Triazoles,
http://linkedlifedata.com/resource/pubmed/chemical/anastrozole,
http://linkedlifedata.com/resource/pubmed/chemical/exemestane,
http://linkedlifedata.com/resource/pubmed/chemical/letrozole
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0167-6806
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
75 Suppl 1
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
S13-7; discussion S33-5
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pubmed:dateRevised |
2005-11-16
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pubmed:meshHeading |
pubmed-meshheading:12353818-Androstadienes,
pubmed-meshheading:12353818-Antineoplastic Agents,
pubmed-meshheading:12353818-Aromatase Inhibitors,
pubmed-meshheading:12353818-Breast Neoplasms,
pubmed-meshheading:12353818-Chemotherapy, Adjuvant,
pubmed-meshheading:12353818-Enzyme Inhibitors,
pubmed-meshheading:12353818-Female,
pubmed-meshheading:12353818-Humans,
pubmed-meshheading:12353818-Nitriles,
pubmed-meshheading:12353818-Triazoles
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pubmed:year |
2002
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pubmed:articleTitle |
New generation aromatase inhibitors--from the advanced to the adjuvant setting.
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pubmed:affiliation |
Department of Medical Oncology, MD Anderson Cancer Center, The University of Texas, Houston 77030-4009, USA. abuzdar@mdanderson.org
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pubmed:publicationType |
Journal Article,
Review
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