Extended Adjuvant Endocrine Therapy in Breast Cancer: Current Status and Future Directions

被引:29
作者
Goss, Paul E. [1 ,2 ]
Muss, Hyman B. [3 ]
Ingle, James N. [4 ]
Whelan, Timothy J. [5 ]
Wu, Melinda [6 ]
机构
[1] Massachusetts Gen Hosp, Ctr Canc, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Univ Vermont, Burlington, VT 05405 USA
[4] Mayo Clin, Div Med Oncol, Rochester, MN USA
[5] McMaster Univ, Juravinski Canc Ctr, Hamilton, ON L8S 4L8, Canada
[6] Univ Toronto, Toronto, ON M5S 1A1, Canada
关键词
Anastrozole; Aromatase inhibitors; Hormone receptor; Letrozole; Tamoxifen;
D O I
10.3816/CBC.2008.n.049
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Women with hormone receptor-positive breast cancer have traditionally been treated with 5 years of adjuvant tamoxifen to reduce their risk of subsequent recurrent disease. Among those who experience subsequent disease recurrence, the majority do so after 5 years, suggesting that longer durations of endocrine therapy might be beneficial. Two options tested include longer tamoxifen and, in postmenopausal women, a switch to an aromatase inhibitor (AI). In the National Cancer Institute of Canada Cooperative Trials Group MA.17 trial, we tested the Al letrozole given to postmenopausal women for 5 years after tamoxifen as extended adjuvant therapy because of its efficacy in patients with advanced breast cancer in progression on previous tamoxifen. The first interim analysis (median, 2.4 patient years) showed substantial benefits from letrozole, and all patients were unblinded and offered the option of letrozole. Despite two thirds of the patients crossing over to letrozole, an intent-to-treat analysis at 54 months' follow-up continued to demonstrate the strong beneficial effect of extended adjuvant letrozole. Furthermore, significant benefit was demonstrated among patients who had been randomized to placebo but elected to take letrozole after a prolonged washout from previous tamoxifen (late extended adjuvant therapy). A trial examining the merits of > 5 years of treatment with an Al, MA.17R, is ongoing, as are a number of other trials of duration of therapy. This article reviews results from MA.17 and the design of these trials of duration.
引用
收藏
页码:411 / 417
页数:7
相关论文
共 48 条
[1]  
*ABCSG, 2007, BREAST CARE, V2, P47
[2]  
Abe O, 2005, LANCET, V365, P1687, DOI 10.1016/s0140-6736(05)66544-0
[3]  
[Anonymous], N ENGL J MED
[4]  
[Anonymous], BREAST CANC RES T S1
[5]  
Barghout V, 2005, BREAST CANCER RES TR, V94, pS97
[6]  
BRYANT J, 2001, J NATL CANC I MONOGR, V30, P56
[7]   Competing causes of death from a randomized trial of extended adjuvant endocrine therapy for breast cancer [J].
Chapman, Judith-Anne W. ;
Meng, Daniel ;
Shepherd, Lois ;
Parulekar, Wendy ;
Ingle, James N. ;
Muss, Hyman B. ;
Palmer, Michael ;
Yu, Changhong ;
Goss, Paul E. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2008, 100 (04) :252-260
[8]   Ten-year outcomes in a population-based cohort of node-negative, lymphatic, and vascular invasion-negative early breast cancers without adjuvant systemic therapies [J].
Chia, SK ;
Speers, CH ;
Bryce, CJ ;
Hayes, MM ;
Olivotto, IA .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (09) :1630-1637
[9]  
*CLINICALTRIALS GO, DIFF DUR ADJ AN THER
[10]  
*CLINICALTRIALS GO, SEC ADJ LONG TERM ST