Adding hormonal therapy to chemotherapy and trastuzumab improves prognosis in patients with hormone receptor-positive and human epidermal growth factor receptor 2-positive primary breast cancer

被引:28
作者
Hayashi, Naoki [1 ,2 ,3 ]
Niikura, Naoki [2 ,4 ]
Yamauchi, Hideko [2 ]
Nakamura, Seigo [2 ,5 ]
Ueno, Naoto T. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Breast Med Oncol, Unit 1354, Houston, TX 77030 USA
[2] St Lukes Int Hosp, Dept Breast Surg Oncol, Chuo Ku, Tokyo 1048560, Japan
[3] Showa Univ, Sch Med, Dept Pathol 2, Shinagawa Ku, Tokyo 1428555, Japan
[4] Tokai Univ, Sch Med, Dept Breast & Endocrine Surg, Isehara, Kanagawa 2591193, Japan
[5] Showa Univ, Dept Breast Surg Oncol, Sch Med, Shinagawa Ku, Tokyo 1428555, Japan
基金
美国国家卫生研究院;
关键词
Hormonal therapy; Hormone receptor; Human epidermal growth factor receptor 2; Breast neoplasm; Chemotherapy; ESTROGEN-RECEPTOR; PROGESTERONE-RECEPTOR; TAMOXIFEN; HER-2; COMBINATION; EXPRESSION; TRIAL; EGF;
D O I
10.1007/s10549-012-2336-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Adjuvant hormonal therapy for hormone receptor (HR)-positive primary breast cancer patients and a human epidermal growth factor receptor 2 (HER2)-targeted agent for HER2-positive primary breast cancer patients are standard treatment. However, it is not well known whether adding hormonal therapy to the combination of preoperative or postoperative chemotherapy and HER2-targeted agent contributes any additional clinical benefit in patients with HR-positive/HER2-positive primary breast cancer regardless of cross-talk between HR and HER2. We retrospectively reviewed records from 897 patients with HR-positive/HER2-positive primary breast cancer with clinical stage I-III disease who underwent surgery between 1988 and 2009. We determined the overall survival (OS) and disease-free survival (DFS) rates according to whether they received hormonal therapy or not and according to the type of hormonal therapy, tamoxifen and aromatase inhibitor, they received. The median followup time was 52.8 months (range 1-294.6 months). Patients who received hormonal therapy with chemotherapy and trastuzumab (n = 128) had significantly higher OS and DFS rates than did those who received only chemotherapy and trastuzumab (n = 46) in log-rank analysis (OS 96.1 vs. 87.0 %, p = 0.023, DFS 86.7 vs. 78.3 %, p = 0.029). There was no statistical difference in OS or DFS between those given an aromatase inhibitor and those given tamoxifen. In multivariate analysis, receiving hormonal therapy in addition to the combination of chemotherapy and trastuzumab was the sole independent prognostic factor for DFS (hazard ratio 0.446; 95 % CI 0.200-0.992; p = 0.048), and there was a similar trend in OS. Our study supported that hormonal therapy, whether in the form of an aromatase inhibitor or tamoxifen, confers a survival benefit when added to chemotherapy and trastuzumab in patients with HR-positive/HER2-positive primary breast cancer. Adjuvant treatment without hormonal therapy is inferior for this patient population.
引用
收藏
页码:523 / 531
页数:9
相关论文
共 32 条
[1]  
Abe O, 2005, LANCET, V366, P2087, DOI 10.1016/s0140-6736(05)66544-0
[2]  
[Anonymous], CLIN CANC RES S
[3]   ESTROGEN-DEPENDENT, TAMOXIFEN-RESISTANT TUMORIGENIC GROWTH OF MCF-7 CELLS TRANSFECTED WITH HER2/NEU [J].
BENZ, CC ;
SCOTT, GK ;
SARUP, JC ;
JOHNSON, RM ;
TRIPATHY, D ;
CORONADO, E ;
SHEPARD, HM ;
OSBORNE, CK .
BREAST CANCER RESEARCH AND TREATMENT, 1992, 24 (02) :85-95
[4]  
Brufsky Adam, 2005, Clin Breast Cancer, V6, P247, DOI 10.3816/CBC.2005.n.027
[5]  
Daly JM, 1997, CANCER RES, V57, P3804
[6]   Benefit from adjuvant tamoxifen therapy in primary breast cancer patients according oestrogen receptor, progesterone receptor, EGF receptor and HER2 status [J].
Dowsett, M ;
Houghton, J ;
Iden, C ;
Salter, J ;
Farndon, J ;
A'Hern, R ;
Sainsbury, R ;
Baum, M .
ANNALS OF ONCOLOGY, 2006, 17 (05) :818-826
[7]   Biomarker changes during neoadjuvant anastrozole, tamoxifen, or the combination: Influence of hormonal status and HER-2 in breast cancer - A study from the IMPACT trialists [J].
Dowsett, M ;
Ebbs, SR ;
Dixon, JM ;
Skene, A ;
Griffith, C ;
Boeddinghaus, I ;
Salter, J ;
Detre, S ;
Hills, M ;
Ashley, S ;
Francis, S ;
Walsh, G ;
Smith, IE .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (11) :2477-2492
[8]  
Dowsett M, 2001, CANCER RES, V61, P8452
[9]   Relationship between quantitative estrogen and progesterone receptor expression and human epidermal growth factor receptor 2 (HER-2) status with recurrence in the arimidex, tamoxifen, alone or in combination trial [J].
Dowsett, Mitch ;
Allred, Craig ;
Knox, Jill ;
Quinn, Emma ;
Salter, Janine ;
Wale, Chris ;
Cuzick, Jack ;
Houghton, Joan ;
Williams, Norman ;
Mallon, Elizabeth ;
Bishop, Hugh ;
Ellis, Ian ;
Larsimont, Denis ;
Sasano, Hironobu ;
Carder, Pauline ;
Cussac, Antonio Llombart ;
Knox, Fiona ;
Speirs, Valerie ;
Forbes, John ;
Buzdar, Aman .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (07) :1059-1065
[10]  
Elledge RM, 1998, CLIN CANCER RES, V4, P7