Aromatase inhibitors versus tamoxifen in premenopausal women with oestrogen receptor-positive early-stage breast cancer treated with ovarian suppression: a patient-level meta-analysis of 7030 women from four randomised trials
Abstract
For women with early-stage oestrogen receptor (ER)-positive breast cancer, adjuvant tamoxifen reduces 15-year breast cancer mortality by a third. Aromatase inhibitors are more effective than tamoxifen in postmenopausal women but are ineffective in premenopausal women when used without ovarian suppression. We aimed to investigate whether premenopausal women treated with ovarian suppression benefit from aromatase inhibitors.
We did a meta-analysis of individual patient data from randomised trials comparing aromatase inhibitors (anastrozole, exemestane, or letrozole) versus tamoxifen for 3 or 5 years in premenopausal women with ER-positive breast cancer receiving ovarian suppression (goserelin or triptorelin) or ablation. We collected data on baseline characteristics, dates and sites of any breast cancer recurrence or second primary cancer, and dates and causes of death. Primary outcomes were breast cancer recurrence (distant, locoregional, or contralateral), breast cancer mortality, death without recurrence, and all-cause mortality. As distant recurrence invariably results in death from breast cancer several years after the occurrence, whereas locoregional recurrence and new contralateral breast cancer are not usually fatal, the distant recurrence analysis is shown separately. Standard intention-to-treat log-rank analyses estimated first-event rate ratios (RR) and their confidence intervals (CIs).
Citation impact
- FWCI
- 49.58
- Percentile
- 100%
- References
- 28
Authors
90- RBRosie BradleyCorresponding
- JBJeremy Braybrooke
- RGRichard Gray
- RKRobert K Hills
- ZLZulian Liu
Topics & keywords
- Aromatase
- Breast cancer
- Tamoxifen
- Clinical trial
- Aromatase inhibitor
- Letrozole
- Exemestane
- Cancer
Funding
- CCConquer Cancer Foundation
- BCBreast Cancer Research Foundation
- AAmgen
- BSBristol-Myers Squibb
- ELEli Lilly and Company
- PPfizer
- AAstraZeneca
- GGlaxoSmithKline
- EExelixis
- LLLes Laboratories Pierre Fabre
- IIncyte
- VVeracyte
- CRCancer Research UK
- UOUniversity of Oxford
- APAstellas Pharma
- IIpsen
- GGenentech
- MRMedical Research Council
- DSDaiichi Sankyo Europe
- CCilag