The Breast International Group 1-98 trial: big results for women with hormone-sensitive early breast cancer

被引:11
作者
Monnier, Alain M. [1 ]
机构
[1] Ctr Hosp A Boulloche, Dept Med Oncol, F-25209 Montbeliard, France
关键词
anastrozole; aromatase inhibitor; disease-free survival; hormone-sensitive breast cancer; letrozole; taraoxifen; AROMATASE INHIBITOR AI; ESTRADIOL E2 LEVELS; POSTMENOPAUSAL WOMEN; PLASMA ESTRADIOL; RANDOMIZED-TRIAL; ADJUVANT TREATMENT; ENDOCRINE THERAPY; UPDATED FINDINGS; PHASE-III; TAMOXIFEN;
D O I
10.1586/14737140.7.5.627
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
As there is a risk for relapse in early breast cancer, especially at 1-3 years post surgery, the need for adjuvant therapy is clear. In terms of disease-free survival, aromatase inhibitors have emerged as superior to tamoxifen for the adjuvant treatment of hormone-sensitive breast cancer in several Phase III clinical trials. Of these trials, the Breast International Group (BIG) 1-98 trial stands out as unique in design, as it is the only trial to address whether an aromatase inhibitor is more effective as initial adjuvant therapy or as sequential therapy with an aromatase inhibitor and tamoxifen in either order and in rigor of end points and safety evaluations. When compared with tamoxifen, letrozole has been shown to significantly reduce recurrence risk in the overall population by 19% and also significantly reduced recurrence risk in the patient subgroups at increased risk: node-positive and previously chemotherapy-treated patients. Letrozole is the only aromatase inhibitor to demonstrate a significant 27% reduction in the risk of distant metastases (p = 0.001) in the clinically relevant, hormone receptor-positive population in the initial adjuvant setting. Recent results also suggest that letrozole in particular reduces the risk of distant metastases early on after initial surgery for breast cancer. This is important, as early distant metastatic events compose the majority of early recurrences and are a well-recognized predictor of breast cancer death. Letrozole has been found to be well tolerated in the initial adjuvant treatment setting, and these data have been confirmed by long-term safety data from the monotherapy analysis in the BIG 1-98 study. Thus far, the results from the BIG 1-98 trial provide clear support for the use of letrozole in the initial adjuvant treatment of breast cancer. Future studies will provide the definitive answer to questions of which initial adjuvant therapy is superior (i.e., anastrozole or letrozole) and information as to the optimal treatment strategy (i.e., initial adjuvant aromatase inhibitor therapy or sequential adjuvant aromatase inhibitor therapy).
引用
收藏
页码:627 / 634
页数:8
相关论文
共 49 条
  • [11] Survival and safety of exemestane versus tamoxifen after 2-3 years' tamoxifen treatment (Intergroup Exemestane Study): a randomised controlled trial
    Coombes, R. C.
    Kilburn, L. S.
    Snowdon, C. F.
    Paridaens, R.
    Coleman, R. E.
    Jones, S. E.
    Jassem, J.
    Van de Velde, C. J. H.
    Delozier, T.
    Alvarez, I.
    Del Mastro, L.
    Ortmann, O.
    Diedrich, K.
    Coates, A. S.
    Bajetta, E.
    Holmberg, S. B.
    Dodwell, D.
    Mickiewicz, E.
    Andersen, J.
    Lonning, P. E.
    Cocconi, G.
    Forbes, J.
    Castiglione, M.
    Stuart, N.
    Stewart, A.
    Fallowfield, L. J.
    Bertelli, G.
    Hall, E.
    Bogle, R. G.
    Carpentieri, M.
    Colajori, E.
    Subar, M.
    Ireland, E.
    Bliss, J. M.
    [J]. LANCET, 2007, 369 (9561) : 559 - 570
  • [12] Coombes RC, 2004, NEW ENGL J MED, V351, P2461
  • [13] A randomized trial of exemestane after two to three years of tamoxifen therapy in postmenopausal women with primary breast cancer
    Coombes, RC
    Hall, E
    Gibson, LJ
    Paridaens, R
    Jassem, J
    Delozier, T
    Jones, SE
    Alvarez, I
    Bertelli, G
    Ortmann, O
    Coates, AS
    Bajetta, E
    Dodwell, D
    Coleman, RE
    Fallowfield, LJ
    Mickiewicz, E
    Andersen, J
    Lonning, PE
    Cocconi, G
    Stewart, A
    Stuart, N
    Snowdon, CF
    Carpentieri, M
    Massimini, G
    Bliss, JM
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (11) : 1081 - 1092
  • [14] DEBOER R, 2006, J CLIN ONCOL, V24, pS582
  • [15] Dixon JM, 2006, ANN ONCOL, V17, P100
  • [16] Dixon JM, 2006, J CLIN ONCOL, V24, p15S
  • [17] Dowsett M, 2006, BREAST CANCER RES TR, V100, pS21
  • [18] Retrospective analysis of time to recurrence in the ATAC trial according to hormone receptor status: An hypothesis-generating study
    Dowsett, M
    Cuzick, J
    Wale, C
    Howell, T
    Houghton, J
    Baum, M
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (30) : 7512 - 7517
  • [19] DOWSETT M, 2005, 28 ANN SAN ANT BREAS
  • [20] Ellis MJ, 2003, CANCER RES, V63, P6523