Abstract | BACKGROUND: The randomized, double-blind Multiple Outcomes of Raloxifene Evaluation (MORE) trial found that 4 years of raloxifene therapy decreased the incidence of invasive breast cancer among postmenopausal women with osteoporosis by 72% compared with placebo. We conducted the Continuing Outcomes Relevant to Evista (CORE) trial to examine the effect of 4 additional years of raloxifene therapy on the incidence of invasive breast cancer in women in MORE who agreed to continue in CORE. METHODS: Women who had been randomly assigned to receive raloxifene (either 60 or 120 mg/day) in MORE were assigned to receive raloxifene (60 mg/day) in CORE (n = 3510), and women who had been assigned to receive placebo in MORE continued on placebo in CORE (n = 1703). Breast cancer incidence was analyzed by a log-rank test, and a Cox proportional hazards model was used to compute hazard ratios (HRs) and 95% confidence intervals (CIs). All statistical tests were two-sided. RESULTS: During the CORE trial, the 4-year incidences of invasive breast cancer and estrogen receptor (ER)-positive invasive breast cancer were reduced by 59% (HR = 0.41; 95% CI = 0.24 to 0.71) and 66% (HR = 0.34; 95% CI = 0.18 to 0.66), respectively, in the raloxifene group compared with the placebo group. There was no difference between the two groups in incidence of ER-negative invasive breast cancer during CORE (P = .86). Over the 8 years of both trials, the incidences of invasive breast cancer and ER-positive invasive breast cancer were reduced by 66% (HR = 0.34; 95% CI = 0.22 to 0.50) and 76% (HR = 0.24; 95% CI = 0.15 to 0.40), respectively, in the raloxifene group compared with the placebo group. During the CORE trial, the relative risk of thromboembolism in the raloxifene group compared with that in the placebo group was 2.17 (95% CI = 0.83 to 5.70). This increased risk, also observed in the MORE trial, persisted over the 8 years of both trials. CONCLUSIONS:
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Authors | Silvana Martino, Jane A Cauley, Elizabeth Barrett-Connor, Trevor J Powles, John Mershon, Damon Disch, Roberta J Secrest, Steven R Cummings, CORE Investigators |
Journal | Journal of the National Cancer Institute
(J Natl Cancer Inst)
Vol. 96
Issue 23
Pg. 1751-61
(Dec 01 2004)
ISSN: 1460-2105 [Electronic] United States |
PMID | 15572757
(Publication Type: Clinical Trial, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents, Hormonal
- Estrogen Receptor Modulators
- Selective Estrogen Receptor Modulators
- Raloxifene Hydrochloride
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Topics |
- Aged
- Antineoplastic Agents, Hormonal
(administration & dosage, therapeutic use)
- Breast Neoplasms
(complications, epidemiology, prevention & control)
- Double-Blind Method
- Drug Administration Schedule
- Estrogen Receptor Modulators
(administration & dosage, therapeutic use)
- Female
- Humans
- Incidence
- Middle Aged
- Osteoporosis, Postmenopausal
(complications)
- Patient Selection
- Raloxifene Hydrochloride
(administration & dosage, therapeutic use)
- Selective Estrogen Receptor Modulators
(therapeutic use)
- Treatment Outcome
- United States
(epidemiology)
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