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Lancet. 2009 Dec 19;374(9707):2055-2063. doi: 10.1016/S0140-6736(09)61523-3. Epub 2009 Dec 10.

Adjuvant chemotherapy and timing of tamoxifen in postmenopausal patients with endocrine-responsive, node-positive breast cancer: a phase 3, open-label, randomised controlled trial.

Author information

1
Loyola University Stritch School of Medicine, Maywood, IL, USA. Electronic address: kalbain@lumc.edu.
2
Southwest Oncology Group Statistical Center, Seattle, WA, USA.
3
University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
4
Ohio State University Health Center, Columbus, OH, USA.
5
Louisiana State University, Shreveport, LA, USA.
6
University of Arizona Cancer Center, Tucson, AZ, USA.
7
Flower Memorial Hospital, Sylvania, OH, USA.
8
Roswell Park Cancer Institute, Buffalo, NY, USA.
9
Mayo Clinic, Rochester, MN, USA.
10
Toronto Sunnybrook Regional Cancer Centre, Toronto, ON, USA.
11
University of Michigan, Ann Arbor, MI, USA.
12
Loyola University Stritch School of Medicine, Maywood, IL, USA.
13
Johns Hopkins Medical Center, Baltimore, MD, USA.
14
University of California, San Francisco, San Francisco, CA, USA.
15
Vermont Cancer Center and University of Vermont, Burlington, VT, USA.
16
The Angeles Clinic and Research Institute, Santa Monica, CA, USA.
17
Baylor College of Medicine, Houston, TX, USA.

Abstract

BACKGROUND:

Tamoxifen is standard adjuvant treatment for postmenopausal women with hormone-receptor-positive breast cancer. We assessed the benefit of adding chemotherapy to adjuvant tamoxifen and whether tamoxifen should be given concurrently or after chemotherapy.

METHODS:

We undertook a phase 3, parallel, randomised trial (SWOG-8814, INT-0100) in postmenopausal women with hormone-receptor-positive, node-positive breast cancer to test two major objectives: whether the primary outcome, disease-free survival, was longer with cyclophosphamide, doxorubicin, and fluorouracil (CAF) given every 4 weeks for six cycles plus 5 years of daily tamoxifen than with tamoxifen alone; and whether disease-free survival was longer with CAF followed by tamoxifen (CAF-T) than with CAF plus concurrent tamoxifen (CAFT). Overall survival and toxicity were predefined, important secondary outcomes for each objective. Patients in this open-label trial were randomly assigned by a computer algorithm in a 2:3:3 ratio (tamoxifen:CAF-T:CAFT) and analysis was by intention to treat of eligible patients. Groups were compared by stratified log-rank tests, followed by Cox regression analyses adjusted for significant prognostic factors. This trial is registered with ClinicalTrials.gov, number NCT00929591.

FINDINGS:

Of 1558 randomised women, 1477 (95%) were eligible for inclusion in the analysis. After a maximum of 13 years of follow-up (median 8.94 years), 637 women had a disease-free survival event (tamoxifen, 179 events in 361 patients; CAF-T, 216 events in 566 patients; CAFT, 242 events in 550 patients). For the first objective, therapy with the CAF plus tamoxifen groups combined (CAFT or CAF-T) was superior to tamoxifen alone for the primary endpoint of disease-free survival (adjusted Cox regression hazard ratio [HR] 0.76, 95% CI 0.64-0.91; p=0.002) but only marginally for the secondary endpoint of overall survival (HR 0.83, 0.68-1.01; p=0.057). For the second objective, the adjusted HRs favoured CAF-T over CAFT but did not reach significance for disease-free survival (HR 0.84, 0.70-1.01; p=0.061) or overall survival (HR 0.90, 0.73-1.10; p=0.30). Neutropenia, stomatitis, thromboembolism, congestive heart failure, and leukaemia were more frequent in the combined CAF plus tamoxifen groups than in the tamoxifen-alone group.

INTERPRETATION:

Chemotherapy with CAF plus tamoxifen given sequentially is more effective adjuvant therapy for postmenopausal patients with endocrine-responsive, node-positive breast cancer than is tamoxifen alone. However, it might be possible to identify some subgroups that do not benefit from anthracycline-based chemotherapy despite positive nodes.

FUNDING:

National Cancer Institute (US National Institutes of Health).

PMID:
20004966
PMCID:
PMC3140679
DOI:
10.1016/S0140-6736(09)61523-3
[Indexed for MEDLINE]
Free PMC Article

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