Celecoxib anti-aromatase neoadjuvant (CAAN) trial for locally advanced breast cancer: preliminary report

被引:34
作者
Chow, LWC [1 ]
Wong, JLN
Toi, M
机构
[1] Univ Hong Kong, Med Ctr, Queen Marys Hosp, Dept Surg,Div Breast Surg, Hong Kong, Hong Kong, Peoples R China
[2] Tokyo Metropolitan Komagome Hosp, Dept Surg, Breast Unit, Tokyo, Japan
关键词
CAAN; COX-2; breast cancer;
D O I
10.1016/S0960-0760(03)00355-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Anti-aromatase therapy is important in the treatment of breast cancer in postmenopausal women. Cyclooxygenase-2 (COX-2) inhibitors have been shown to be effective in chemoprevention in animal and clinical studies. A proof of principle study was performed to investigate the efficacy of combing anti-aromatase therapy (exemestane) and COX-2 inhibitors neoadjuvantly in hormone-sensitive postmenopausal breast cancers. The initial results are reported. The patients were randomly assigned to receive exemestane 25 mg daily and celecoxib 400 mg twice daily (group A), exemestane 25 mg daily (group B) and letrozole 2.5 mg daily (group C). The analysis was based on 20 patients who received at least one cycle of treatment. Fourteen patients completed two cycles and 12 patients three cycles. All groups showed clinical response and there was decrease in tumor area in each group. However, complete clinical response was only observed for group A patients. There was also progressive decline in blood CEA and CA15.3 levels but the differences between the three groups were not significant. The results of the preliminary analysis are encouraging but definitive conclusion could only be drawn after the completion of the study. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:443 / 447
页数:5
相关论文
共 21 条
[1]   Correlation of aromatase and cyclooxygenase gene expression in human breast cancer specimens [J].
Brueggemeier, RW ;
Quinn, AL ;
Parrett, ML ;
Joarder, FS ;
Harris, RE ;
Robertson, FM .
CANCER LETTERS, 1999, 140 (1-2) :27-35
[2]  
Chow LWC, 1997, CHINESE MED J-PEKING, V110, P474
[3]  
Chow LWC, 2000, J SURG ONCOL, V75, P172, DOI 10.1002/1096-9098(200011)75:3<172::AID-JSO4>3.0.CO
[4]  
2-A
[5]  
Dixon JM, 2000, CLIN CANCER RES, V6, P2229
[6]  
Forrest A P, 1982, J R Coll Surg Edinb, V27, P253
[7]   ASPIRIN AND THE RISK OF COLORECTAL-CANCER IN WOMEN [J].
GIOVANNUCCI, E ;
EGAN, KM ;
HUNTER, DJ ;
STAMPFER, MJ ;
COLDITZ, GA ;
WILLETT, WC ;
SPEIZER, FE .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (10) :609-614
[8]  
Goss Paul, 2002, Cancer Control, V9, P2
[9]   Nonsteroidal antiinflammatory drugs and breast cancer [J].
Harris, RE ;
Namboodiri, KK ;
Farrar, WB .
EPIDEMIOLOGY, 1996, 7 (02) :203-205
[10]  
Harris RE, 2000, CANCER RES, V60, P2101