Phase III, multicenter, double-blind, randomized study of letrozole, an aromatase inhibitor, for advanced breast cancer versus megestrol acetate

被引:269
作者
Buzdar, A
Douma, J
Davidson, N
Elledge, R
Morgan, M
Smith, R
Porter, L
Nabholtz, J
Xiang, X
Brady, C
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Breast Med Oncol, Houston, TX 77030 USA
[2] Baylor Coll Med, Houston, TX 77030 USA
[3] St Thomas Med Grp, Nashville, TN USA
[4] Baptist Med Ctr, Columbia, SC USA
[5] Ziekenhuis Rijnstate, Arnhem, Netherlands
[6] N Middlesex Hosp, London N18 1QX, England
[7] Cross Canc Inst, Edmonton, AB T6G 1Z2, Canada
关键词
D O I
10.1200/JCO.2001.19.14.3357
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To compare two doses of letrozole (0.5 mg and 2.5 mg every day) and megestrol acetate (40 mg qid) as endocrine therapy in postmenopausal women with advanced breast cancer previously treated with antiestrogens. Patient and Methods: This double-blind, randomized, multicenter, multinational study enrolled 602 patients, all of whom were included in the primary analysis in the protocol. Patients had advanced or metastatic breast cancer with evidence of disease progression while receiving continuous adjuvant antiestrogen therapy, held experienced relapse within 12 months of stopping adjuvant antiestrogen therapy given for at least 6 months, or had experienced disease progression while receiving antiestrogen therapy for advanced disease. Tumors were required to be estrogen receptor and/or progesterone receptor-positive or of unknown status. Confirmed objective response rate was the primary efficacy variable. Karnofsky Performance Status and European Organization for Research and Treatment of Cancer quality-of-life assessments were collected for 1 year. Results: There were no statistically significant differences among the three treatment groups for overall objective tumor response. Patients treated with letrozole 0.5 mg had improvements in disease progression (P = .044) and a decreased risk of treatment failure (P = .018), compared with patients treated with megestrol acetate. Letrozole 0.5 mg showed a trend (P = .053) for survival benefit when compared with megestrol acetate. Megestrol acetate was more likely to produce weight gain, dyspnea, and vaginal bleeding, and the letrozole groups were more likely to experience headache, hair thinning, and diarrhea. Conclusion: Given a favorable tolerability profile, once-daily dosing, and evidence of clinically relevant benefit, letrozole is equivalent to megestrol acetate and should be considered for use as an alternative treatment of advanced breast cancer in postmenopausal women after treatment failure with antiestrogens. (C) 2001 by American Society of Clinical Oncology.
引用
收藏
页码:3357 / 3366
页数:10
相关论文
共 25 条
  • [1] Aaronson NK, 1991, EFFECT CANC QUALITY, P185
  • [2] HIGHLY SELECTIVE-INHIBITION OF ESTROGEN BIOSYNTHESIS BY CGS-20267, A NEW NONSTEROIDAL AROMATASE INHIBITOR
    BHATNAGAR, AS
    HAUSLER, A
    SCHIEWECK, K
    LANG, M
    BOWMAN, R
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1990, 37 (06) : 1021 - 1027
  • [3] Buzdar AU, 1997, CANCER, V79, P730, DOI 10.1002/(SICI)1097-0142(19970215)79:4<730::AID-CNCR10>3.0.CO
  • [4] 2-0
  • [5] Chaudri HA, 1999, J CLIN ONCOL, V17, P3859
  • [6] Predictors of response to second-line endocrine therapy for breast cancer
    Cheung, KL
    Willsher, PC
    Pinder, SE
    Ellis, IO
    Elston, CW
    Nicholson, RI
    Blamey, RW
    Robertson, JFR
    [J]. BREAST CANCER RESEARCH AND TREATMENT, 1997, 45 (03) : 219 - 224
  • [7] THE EFFICACY OF CGS-20267 IN SUPPRESSING ESTROGEN BIOSYNTHESIS IN PATIENTS WITH ADVANCED STAGE BREAST-CANCER
    DEMERS, LM
    LIPTON, A
    HARVEY, HA
    KAMBIC, KB
    GROSSBERG, H
    BRADY, C
    SANTEN, RJ
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1993, 44 (4-6) : 687 - 691
  • [8] Letrozole, a new oral aromatase inhibitor for advanced breast cancer: Double-blind randomized trial showing a dose effect and improved efficacy and tolerability compared with megestrol acetate
    Dombernowsky, P
    Smith, I
    Falkson, G
    Leonard, R
    Panasci, L
    Bellmunt, J
    Bezwoda, W
    Gardin, G
    Gudgeon, A
    Morgan, M
    Fornasiero, A
    Hoffmann, W
    Michel, J
    Hatschek, T
    Tjabbes, T
    Chaudri, HA
    Hornberger, U
    Trunet, PF
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (02) : 453 - 461
  • [9] Letrozole, a new oral aromatase inhibitor: Randomised trial comparing 2.5mg daily, 0.5mg daily and aminoglutethimide in postmenopausal women with advanced breast cancer
    Gershanovich, M
    Chaudri, HA
    Campos, D
    Lurie, H
    Bonaventura, A
    Jeffrey, M
    Buzzi, F
    Bodrogi, I
    Ludwig, H
    Reichardt, P
    O'Higgins, N
    Romieu, G
    Friederich, P
    Lassus, M
    [J]. ANNALS OF ONCOLOGY, 1998, 9 (06) : 639 - 645
  • [10] The third-generation non-steroidal aromatase inhibitors: A review of their clinical benefits in the second-line hormonal treatment of advanced breast cancer
    Hamilton, A
    Piccart, M
    [J]. ANNALS OF ONCOLOGY, 1999, 10 (04) : 377 - 384