論文

査読有り
2005年10月

Serum lipid profiles in patients receiving endocrine treatment for breast cancer - the results from the Celecoxib Anti-Aromatase Neoadjuvant (CAAN) Trial

BIOMEDICINE & PHARMACOTHERAPY
  • LWC Chow
  • ,
  • CWL Cheng
  • ,
  • JLN Wong
  • ,
  • M Toi

59
SUPPL. 2
開始ページ
S302
終了ページ
S305
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/S0753-3322(05)80051-4
出版者・発行元
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER

Background. - Anti-aromatase therapy is important in the treatment of breast cancer. Cyclooxygenase-2 (COX-2) inhibitors may be effective in chernoprevention. A proof of principle study was performed to investigate the efficacy and side effects including changes in lipid profiles of combining anti-aromatase therapy and COX-2 inhibitor preoperatively in hormone sensitive postmenopausal breast cancers.
Methods. - From February 2002 to April 2003, 41 postmenopausal women with histologically proven LABC were recruited. The patients were randomly assigned to receive exemestane 25 mg daily and celecoxib 400 mg twice-daily (group A), exemestane 25 mg daily (group 13) and letrozole 2.5 mg daily (group Q.
Results. - Observed clinical response rates were 61.5%, 60% and 54.5% for Groups A-C, respectively, with no pathologic complete response. Cholesterol levels for Group A dropped progressively and a statistical difference was observed between fifth week after operation and preoperative level (P = 0.026). In addition, Group A has significantly lowered cholesterol and LDL levels than Groups B and C after 18 weeks of treatment.
Conclusion. - The initial results show that different neoadjuvant anti-aromatase therapies has similar efficacy but the combination with celecoxib may have an advantageous effects on the serum lipid profiles. (c) 2005 Elsevier SAS. All rights reserved.

リンク情報
DOI
https://doi.org/10.1016/S0753-3322(05)80051-4
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000234423600011&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/S0753-3322(05)80051-4
  • ISSN : 0753-3322
  • Web of Science ID : WOS:000234423600011

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