American Society of Clinical Oncology technology assessment of pharmacologic interventions for breast cancer risk reduction including tamoxifen, raloxifene, and aromatase inhibition

被引:142
作者
Chlebowski, RT [1 ]
Col, N [1 ]
Winer, EP [1 ]
Collyar, DE [1 ]
Cummings, SR [1 ]
Vogel, VG [1 ]
Burstein, HJ [1 ]
Eisen, A [1 ]
Lipkus, I [1 ]
Pfister, DG [1 ]
机构
[1] Amer Soc Clin Oncol, Hlth Serv Res Dept, Alexandria, VA 22314 USA
关键词
D O I
10.1200/JCO.2002.06.029
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective : To update an evidence-based technology assessment of chemoprevention strategies for breast cancer risk reduction. Potential Interventions: Tamoxifen, raloxifene, aromatase inhibition, and fenretinide. Outcomes: Outcomes of interest include breast cancer incidence, breast cancer-specific survival, overall survival, and net health benefit. Evidence: A comprehensive, formal literature review was conducted for relevant topics. Testimony was collected from invited experts and interested parties. The American Society of Clinical Oncology (ASCO) prescribed technology assessment procedure was followed. Values: More weight was given to published randomized trials. Benefits/Harms: A woman's decision regarding breast cancer risk reduction strategies is complex and will depend on the importance and weight attributed to information regarding both cancer- and noncancer-related risks and benefits. Conclusions: For women with a defined 5-year projected breast cancer risk of : 1.66%, tamoxifen (at 20 mg/d for 5 years) may be offered to reduce their risk. Risk/benefit models suggest that greatest clinical benefit with least side effects is derived from use of tamoxifen in younger (premenopausal) women (who are less likely to have thromboembolic sequelae and uterine cancer), women without a uterus, and women at higher breast cancer risk. Data do not as yet suggest that tamoxifen provides an overall health benefit or increases survival. In all circumstances, tamoxifen use should be discussed as part of an informed decision-making process with careful consideration of individually calculated risks and benefits. Use of tamoxifen combined with hormone replacement therapy or use of raloxifene, any aromatase inhibitor or inactivator, or fenretinide to lower the risk of developing breast cancer is not recommended outside of a clinical trial setting. This technology assessment represents an ongoing process and recommendations will be updated in a timely matter. Validation: The conclusions were endorsed by the ASCO Health Services Research Committee and the ASCO Board of Directors. Sponsor : American Society of Clinical Oncology. (C) 2002 by American Society of Clinical Oncology.
引用
收藏
页码:3328 / 3343
页数:16
相关论文
共 121 条
  • [1] Anderson G, 1998, CONTROL CLIN TRIALS, V19, P61
  • [2] [Anonymous], 1988, CLIN CHEM
  • [3] Assessing the risk of breast cancer.
    Armstrong, K
    Eisen, A
    Weber, B
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (08) : 564 - 571
  • [4] Effect of adjuvant tamoxifen on the endometrium in women with breast cancer: A prospective study using office endometrial biopsy
    Barakat, RR
    Gilewski, TA
    Almadrones, L
    Saigo, PE
    Venkatraman, E
    Hudis, C
    Hoskins, WJ
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (20) : 3459 - 3463
  • [5] Raloxifene and cardiovascular events in osteoporotic postmenopausal women - Four-year results from the MORE (Multiple Outcomes of Raloxifene Evaluation) randomized trial
    Barrett-Connor, E
    Grady, D
    Sashegyi, A
    Anderson, PW
    Cox, DA
    Hoszowski, K
    Rautaharju, P
    Harper, KD
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 287 (07): : 847 - 857
  • [6] Women's interest in chemoprevention for breast cancer
    Bastian, LA
    Lipkus, IM
    Kuchibhatla, MN
    Weng, HH
    Halabi, S
    Ryan, PD
    Skinner, CS
    Rimer, BK
    [J]. ARCHIVES OF INTERNAL MEDICINE, 2001, 161 (13) : 1639 - 1644
  • [7] Baum M, 2001, BREAST CANCER RES TR, V69, P210
  • [8] Beral V, 1997, LANCET, V350, P1047, DOI 10.1016/S0140-6736(97)08233-0
  • [9] Effect of endocrine treatment on sexuality in premenopausal breast cancer patients:: A prospective randomized study
    Berglund, G
    Nystedt, M
    Bolund, C
    Sjödén, PO
    Rutquist, LE
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (11) : 2788 - 2796
  • [10] Risk and prognosis of endometrial cancer after tamoxifen for breast cancer
    Bergman, L
    Beelen, MLR
    Gallee, MPW
    Hollema, H
    Benraadt, J
    van Leeuwen, FE
    [J]. LANCET, 2000, 356 (9233) : 881 - 887