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Timing of CMF chemotherapy in combination with tamoxifen in postmenopausal women with breast cancer: role of endocrine responsiveness of the tumor.

Authors :
Colleoni M
Li S
Gelber RD
Coates AS
Castiglione-Gertsch M
Price KN
Lindtner J
Rudenstam CM
Crivellari D
Collins J
Pagani O
Simoncini E
Thürlimann B
Murray E
Forbes J
Erzen D
Holmberg S
Veronesi A
Goldhirsch A
Source :
Annals of oncology : official journal of the European Society for Medical Oncology [Ann Oncol] 2005 May; Vol. 16 (5), pp. 716-25. Date of Electronic Publication: 2005 Apr 07.
Publication Year :
2005

Abstract

Background: Controversy persists about whether chemotherapy benefits all breast cancer patients.<br />Patients and Methods: In the International Breast Cancer Study Group (IBCSG) trial VII, 1212 postmenopausal patients with node-positive disease were randomized to receive tamoxifen for 5 years or tamoxifen plus three concurrent courses of cyclophosphamide, methotrexate and 5-fluorouracil ('classical' CMF) chemotherapy, either early, delayed or both. In IBCSG trial IX, 1669 postmenopausal patients with node-negative disease were randomized to receive either tamoxifen alone or three courses of adjuvant classical CMF prior to tamoxifen. Results were assessed according to estrogen receptor (ER) content of the primary tumor.<br />Results: For patients with node-positive, ER-positive disease, adding CMF either early, delayed or both reduced the risk of relapse by 21% (P=0.06), 26% (P=0.02) and 25% (P=0.02), respectively, compared with tamoxifen alone. There was no difference in disease-free survival when CMF was given prior to tamoxifen in patients with node-negative, ER-positive tumors.<br />Conclusions: CMF given concurrently (early, delayed or both) with tamoxifen was more effective than tamoxifen alone for patients with node-positive, endocrine-responsive breast cancer, supporting late administration of chemotherapy even after commencement of tamoxifen. In contrast, sequential CMF and tamoxifen for patients with node-negative, endocrine-responsive disease was ineffective.

Details

Language :
English
ISSN :
0923-7534
Volume :
16
Issue :
5
Database :
MEDLINE
Journal :
Annals of oncology : official journal of the European Society for Medical Oncology
Publication Type :
Academic Journal
Accession number :
15817593
Full Text :
https://doi.org/10.1093/annonc/mdi163