Increase in response rate by prolonged treatment with neoadjuvant letrozole

被引:105
作者
Dixon, J. Michael [1 ]
Renshaw, Lorna [1 ]
Macaskill, E. Jane [1 ]
Young, Oliver [1 ]
Murray, Juliette [1 ]
Cameron, David [1 ]
Kerr, Gillian R. [1 ]
Evans, Dean B. [2 ]
Miller, William R. [1 ]
机构
[1] Western Gen Hosp, Edinburgh Breast Unit, Edinburgh EH4 2XU, Midlothian, Scotland
[2] Novartis Pharma AG, CH-4002 Basel, Switzerland
关键词
Breast conserving surgery; Endocrine therapy; Neoadjuvant; Letrozole; Large operable and locally advanced breast cancer; OPERABLE BREAST-CANCER; SURGERY PLUS TAMOXIFEN; TERM-FOLLOW-UP; ELDERLY-PATIENTS; PREOPERATIVE CHEMOTHERAPY; ENDOCRINE THERAPY; RANDOMIZED-TRIAL; MASTECTOMY; WOMEN;
D O I
10.1007/s10549-008-9915-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose The aim of this study was to investigate the potential benefits of prolonged treatment with neoadjuvant letrozole. Patients and Methods About 182 consecutive patients have been treated in Edinburgh with neoadjuvant letrozole for 3 months or longer and 63 patients have continued on letrozole beyond 3 months. Outcomes are reported. Results Of the 63 patients who continued on letrozole, 38 patients took letrozole for more than 1 year and 23 took letrozole for more than 24 months. The median reduction in clinical volume in the first 3 months in these 63 patients was 52%. Similar reductions in median clinical volume were seen between three to 6 months (50%), 6-12 months and 12-24 months (medians 37 and 33%, respectively). At 3 months 69.8% of the 182 patients had a partial or complete response. The response rate increased to 83.5% with prolonged letrozole treatment. Continuing letrozole beyond 3 months increased the number of women who initially required mastectomy or had locally advanced breast cancer who were subsequently suitable for breast conserving surgery from 60% (81/134) at 3 months to 72% (96/134). Thirty-three women remain on letrozole alone (man age at diagnosis 83 years) and at 3 years the median time to treatment failure has not been reached. Conclusion Continuing letrozole in responding patients beyond 3-4 months achieves further clinical reduction in tumour size. For elderly women with a short life expectancy letrozole alone may provide long-term disease control.
引用
收藏
页码:145 / 151
页数:7
相关论文
共 27 条
[1]
BATES T, 2001, EUR J CANC S5, V37
[2]
BEAR H, 1998, SEMIN ONCOL S3, V25, pS3
[3]
Bear HD, 2004, BREAST CANCER RES TR, V88, pS16
[4]
PRIMARY CHEMOTHERAPY TO AVOID MASTECTOMY IN TUMORS WITH DIAMETERS OF 3 CENTIMETERS OR MORE [J].
BONADONNA, G ;
VERONESI, U ;
BRAMBILLA, C ;
FERRARI, L ;
LUINI, A ;
GRECO, M ;
BARTOLI, C ;
DEYOLDI, GC ;
ZUCALI, R ;
RILKE, F ;
ANDREOLA, S ;
SILVESTRINI, R ;
DIFRONZO, G ;
VALAGUSSA, P .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1990, 82 (19) :1539-1545
[5]
Capasso I, 2000, ANN ONCOL, V11, P20
[6]
Good clinical response of breast cancers to neoa uvant chemoendocrine therapy is associated with improved overall survival [J].
Cleator, SJ ;
Makris, A ;
Ashley, SE ;
Lal, R ;
Powles, TJ .
ANNALS OF ONCOLOGY, 2005, 16 (02) :267-272
[7]
Surgical issues surrounding use of aromatase inhibitors [J].
Dixon, JM ;
Renshaw, L ;
Murray, J ;
Macaskill, EJ ;
Young, O ;
Miller, WR .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2005, 95 (1-5) :97-103
[8]
Neoadjuvant tamoxifen and aromatase inhibitors: comparisons and clinical outcomes [J].
Dixon, JM ;
Jackson, J ;
Renshaw, L ;
Miller, WR .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2003, 86 (3-5) :295-299
[9]
Letrozole as primary medical therapy for locally advanced and large operable breast cancer [J].
Dixon, JM ;
Love, CDB ;
Bellamy, COC ;
Cameron, DA ;
Leonard, RCF ;
Smith, H ;
Miller, WR .
BREAST CANCER RESEARCH AND TREATMENT, 2001, 66 (03) :191-199
[10]
Preoperative treatment of postmenopausal breast cancer patients with letrozole: A randomized double-blind multicenter study [J].
Eiermann, W ;
Paepke, S ;
Appfelstaedt, J ;
Llombart-Cussac, A ;
Eremin, J ;
Vinholes, J ;
Mauriac, L ;
Ellis, M ;
Lassus, M ;
Chaudri-Ross, HA ;
Dugan, M ;
Borgs, M ;
Semiglazov, V .
ANNALS OF ONCOLOGY, 2001, 12 (11) :1527-1532