FULVESTRANT - A NOVEL ESTROGEN RECEPTOR ANTAGONIST FOR THE TREATMENT OF ADVANCED BREAST CANCER

被引:0
|
作者
Buzdar, Aman U. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
关键词
D O I
10.1358/dot.2008.44.9.1269854
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Endocrine therapy is often the preferred treatment option for postmenopausal women with hormone receptor-positive breast cancer. However, as many patients eventually develop resistance there is a need for novel, efficacious and well-tolerated treatments that lack cross-resistance with current therapies. This review describes the development of fulvestrant (Faslodex (TM)), an estrogen receptor antagonist with a different and distinct mode of action and no agonist effects. Phase III clinical trials in postmenopausal women with advanced breast cancer have found fulvestrant at the approved dose of 250 mg/month to be at least as effective and well tolerated as anastrozole following disease progression or recurrence on tamoxifen, and as effective as exemestane following disease progression or recurrence on nonsteroidal aromatase inhibitors. In addition, fulvestrant has also demonstrated activity in patients with visceral and HER2+ disease, who are generally regarded as being less responsive to endocrine therapy. Data from a recent neoadjuvant study suggest that a higher dose of fulvestrant may possess greater activity. Trials evaluating higher fulvestrant doses, and regimens combining fulvestrant with aromatase inhibitors or agents targeting growth factor receptors, are ongoing and will help determine the optimum use of fulvestrant in the endocrine treatment sequence for postmenopausal women with advanced breast cancer. Copyright 2008 Prous Science, S.A.U. or its licensors. All rights reserved.
引用
收藏
页码:679 / 692
页数:14
相关论文
共 50 条
  • [1] Fulvestrant - A new type of estrogen receptor antagonist for the treatment of advanced breast cancer
    Buzdar, AU
    DRUGS OF TODAY, 2004, 40 (09): : 751 - 764
  • [2] Fulvestrant: An estrogen receptor antagonist that downregulates the estrogen receptor
    Jones, SE
    SEMINARS IN ONCOLOGY, 2003, 30 (05) : 14 - 20
  • [3] Fulvestrant for the treatment of advanced breast cancer
    Blackburn, Sophie A.
    Parks, Ruth M.
    Cheung, Kwok-Leung
    EXPERT REVIEW OF ANTICANCER THERAPY, 2018, 18 (07) : 619 - 628
  • [4] The estrogen receptor antagonist fulvestrant, but not the partial antagonist tamoxifen, is an effective endocrine treatment in a xenograft model of HER2 overexpressing breast cancer.
    Massarweh, S
    Shou, J
    Mollsin, SK
    Hilsenbeck, S
    DiPietro, M
    Wakeling, A
    Osborne, CK
    Schiff, R
    BREAST CANCER RESEARCH AND TREATMENT, 2002, 76 : S71 - S71
  • [5] Fulvestrant in the treatment of postmenopausal women with advanced breast cancer
    Gradishar, W
    EXPERT REVIEW OF ANTICANCER THERAPY, 2005, 5 (03) : 445 - 453
  • [6] Clinical efficacy of fulvestrant and effects on estrogen receptor levels during first-line endocrine treatment of patients with advanced breast cancer
    Robertson, JFR
    Gutteridge, E
    Cheung, KL
    Pinder, S
    Wakeling, A
    BREAST CANCER RESEARCH AND TREATMENT, 2004, 88 : S236 - S237
  • [7] Effects of fulvestrant on estrogen receptor levels during long-term treatment of patients with advanced breast cancer - final results.
    Gutteridge, E
    Robertson, JFR
    Cheung, KL
    Pinder, S
    Wakeling, A
    BREAST CANCER RESEARCH AND TREATMENT, 2004, 88 : S177 - S177
  • [8] Tolerability and efficacy of 500 mg fulvestrant in postmenopausal women with estrogen receptor (ER) plus advanced breast cancer
    Come, S. E.
    Parker, L. M.
    Wulf, G.
    Kuter, I.
    Ryan, P. D.
    Tkaczuk, K.
    Borges, V.
    Kasper, H.
    Gelman, R.
    Winer, E. P.
    JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (15)
  • [10] Endocrine treatment options for advanced breast cancer - the role of fulvestrant
    Robertson, JFR
    Come, SE
    Jones, SE
    Beex, L
    Kaufmann, M
    Makris, A
    Nortier, JWR
    Possinger, K
    Rutqvist, LE
    EUROPEAN JOURNAL OF CANCER, 2005, 41 (03) : 346 - 356