Identifying breast cancer patients most likely to benefit from aromatase inhibitor therapy after adjuvant radiation and tamoxifen

被引:5
作者
Freedman, Gary M.
Anderson, Penny
Li, Tianyu
Ross, Eric
Swaby, Ramona
Goldstein, Lori
机构
[1] Fox Chase Canc Ctr, Dept Radiat Oncol, Philadelphia, PA 19111 USA
[2] Fox Chase Canc Ctr, Dept Biostat, Philadelphia, PA 19111 USA
[3] Fox Chase Canc Ctr, Dept Med Oncol, Philadelphia, PA 19111 USA
关键词
breast cancer; radiation therapy; hormonal therapy; event-free survival;
D O I
10.1002/cncr.22291
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. The purpose of the current study was to examine patient selection for an aromatase inhibitor in breast cancer patients who were free from adverse events 5 years after treatment with tamoxifen. METHODS. In all, 471 women were treated with breast-conserving surgery, axillary lymph node dissection, and radiation. Eligibility included T1-2 disease, tamoxifen use, follow-up of >= 5 years, no prior breast cancer, and freedom from all events at 5 years of follow-up. Patients treated with chemotherapy more often had T2 disease and positive lymph nodes, and were aged < 60 years compared with patients treated with tamoxifen alone. No patient during the period of the current study (1982-1999) received an aromatase inhibitor. The median follow-up was 8.25 years. RESULTS. There were 36 events: 10 contralateral breast cancers (CBCs) and 26 recurrences (8 local, I regional, and 17 distant). The 10-year risk of locoregional recurrence was 2.5%, the 10-year risk of CBC was 3.6%, and the 10-year risk of distant metastasis was 4.4%. The event-free survival rate for all patients was 93%. Only >= 4 positive lymph nodes and premenopausal status were found to be independent variables for decreased event-free survival on multivariate analysis. The overall survival rate was 89%. Only younger age and lower lymph node status were found to be significant predictors of improved overall survival. CONCLUSIONS. In the current study, a 40% reduction in recurrence/CBC with the addition of an aromatase inhibitor after 5 years of tamoxifen treatment would have had a marginal benefit of 1% to 2%. Women who were premenopausal and patients with >= 4 positive lymph nodes would have the greatest absolute benefit of > 3% in the 10-year event-free survival rate from extended therapy. The decision needs to be individualized for patients aged >= 60 years based on their initial lymph node status and the presence of comorbidities that could lower their 5-year life expectancy.
引用
收藏
页码:2552 / 2558
页数:7
相关论文
共 9 条
[1]  
[Anonymous], 2004, Bone Health and Osteoporosis: A report of the Surgeon General
[2]   Cyclophosphamide, methotrexate, and fluorouracil versus tamoxifen plus ovarian suppression as adjuvant treatment of estrogen receptor-positive pre-/perimenopausal breast cancer patients: Results of the Italian Breast Cancer Adjuvant Study Group 02 Randomized Trial [J].
Boccardo, F ;
Rubagotti, A ;
Amoroso, D ;
Mesiti, M ;
Romeo, D ;
Sismondi, P ;
Giai, M ;
Genta, F ;
Pacini, P ;
Distante, V ;
Bolognesi, A ;
Aldrighetii, D ;
Farris, A .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (14) :2718-2727
[3]  
*EARL BREAST CANC, 2005, LANCET, V65, P1687
[4]   Five versus more than five years of tamoxifen for lymph node-negative breast cancer: Updated findings from the National Surgical Adjuvant Breast and Bowel Project B-14 randomized trial [J].
Fisher, B ;
Dignam, J ;
Bryant, J ;
Wolmark, N .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2001, 93 (09) :684-690
[5]  
FOWBLE B, 2000, CLIN RAD ONCOLOGY IN
[6]   Randomized trial of letrozole following tamoxifen as extended adjuvant therapy in receptor-positive breast cancer: Updated findings from NCICCTG MA.17 [J].
Goss, PE ;
Ingle, JN ;
Martino, S ;
Robert, NJ ;
Muss, HB ;
Piccart, MJ ;
Castiglione, M ;
Tu, DS ;
Shepherd, LE ;
Pritchard, KI ;
Livingston, RB ;
Davidson, NE ;
Norton, L ;
Perez, EA ;
Abrams, JS ;
Cameron, DA ;
Palmer, MJ ;
Pater, JL .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (17) :1262-1271
[7]  
Greene FL., 2002, AJCC CANC STAGING HD, V6th
[8]  
*NAT COMPR CANC NE, 2005, NCCN PRACT GUID BREA
[9]   Annual hazard rates of recurrence for breast cancer after primary therapy [J].
Saphner, T ;
Tormey, DC ;
Gray, R .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (10) :2738-2746