aTTom: Long-term effects of continuing adjuvant tamoxifen to 10 years versus stopping at 5 years in 6,953 women with early breast cancer.

Author:

Gray Richard G.1,Rea Daniel2,Handley Kelly2,Bowden Sarah Jane2,Perry Philip3,Earl Helena Margaret4,Poole Christopher John5,Bates Tom6,Chetiyawardana Shan7,Dewar John A.8,Fernando Indrajit Nalinika7,Grieve Robert9,Nicoll Jonathan10,Rayter Zenor11,Robinson Anne12,Salman Asad13,Yarnold John14,Bathers Sarah2,Marshall Andrea15,Lee Martin16,

Affiliation:

1. University of Oxford, Oxford, United Kingdom

2. University of Birmingham, Birmingham, United Kingdom

3. AO Foundation, Zurich, Switzerland

4. NIHR Cambridge Biomedical Research Centre, Cambridge, United Kingdom

5. Department of Medical Oncology, Arden Cancer Centre, University Hospital Coventry and Warwickshire and University of Warwick, Coventry, United Kingdom

6. William Harvey Hospital, Ashford, United Kingdom

7. University Hospital Birmingham NHS Foundation Trust, Birmingham, United Kingdom

8. University of Dundee, Dundee, United Kingdom

9. University Hospital, Coventry, United Kingdom

10. North Cumbria University Hospitals, Carlisle, United Kingdom

11. University of Bristol NHS Foundation Trust, Bristol, United Kingdom

12. Southend University Hospital, Southend, United Kingdom

13. Worthing Hospital, Worthing, United Kingdom

14. The Royal Marsden NHS Foundation Trust, Sutton, United Kingdom

15. Warwick Clinical Trials Unit, University of Warwick, Coventry, United Kingdom

16. Arden NHS, Coventry, United Kingdom

Abstract

5 Background: In estrogen-receptor-positive (ER+) early breast cancer, 5 years of tamoxifen reduces breast cancer death rates by about a third throughout years 0-14. It has been uncertain how 10 years of tamoxifen compares with this. Methods: During 1991-2005, 6,953 women with ER+ (n=2755), or ER untested (4198, estimated 80% ER+ if status known) invasive breast cancer from 176 UK centres were, after 5 years of tamoxifen, randomized to stop tamoxifen or continue to year 10. Annual follow-up recorded compliance, recurrence, mortality, and hospital admissions. Results: Allocation to continue tamoxifen reduced breast cancer recurrence (580/3468 vs 672/3485, p=0.003). This reduction was time dependent: rate ratio 0.99 during years 5-6 [95%CI 0.86-1.15], 0.84 [0.73-0.95] during years 7-9, and 0.75 [0.66-0.86] later. Longer treatment also reduced breast cancer mortality (392 vs 443 deaths after recurrence, p=0.05), rate ratio 1.03 [0.84-1.27] during years 5-9 and 0.77 [0.64-0.92] later; and overall mortality (849 vs 910 deaths, p=0.1), rate ratio 1.05 [0.90-1.22] during years 5-9 and 0.86 [0.75-0.97] later. Non-breast-cancer mortality was little affected (457 vs 467 deaths, rate ratio 0.94 [0.82-1.07]). There were 102 vs 45 endometrial cancers RR=2.20 (1.31-2.34, p<0.0001) with 37 (1.1%) vs 20 (0.6%) deaths (absolute hazard 0.5%, p=0.02). Combining the similar results of aTTom and its international counterpart ATLAS (Lancet 2013) enhances statistical significance of recurrence (p<0.0001), breast cancer mortality (p=0.002) and overall survival (p=0.005) benefits. Conclusions: aTTom confirms that, in ER+ disease, continuing tamoxifen to year 10 rather than just to year 5 produces further reductions in recurrence, from year 7 onward, and breast cancer mortality after year 10. Taken together with the reduction in breast cancer deaths seen in trials of 5 years of tamoxifen vs none, these results indicate that 10 years of adjuvant tamoxifen, compared to no tamoxifen, reduces breast cancer mortality by about one third in the first 10 years following diagnosis and by a half subsequently. Clinical trial information: ISRCTN17222211.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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