Question explored with the scientific record
Conversation so far
- 1 can anastrazole be stopped after 2 years
- 2 How much higher is my recurrence risk if I stop after 2 years?
- 3 What are the risks of stopping anastrozole at 2 years for ER+ tumors?
Answered on this page ↓
What are the risks of stopping anastrozole at 2 years for ER+ tumors?
The short version: the evidence you are looking for does not exist, and the closest trial tested a different question.
No trial has ever randomly assigned women to stop anastrozole at 2 years versus continue to 5 years. The ATAC trial compared 5 years of anastrozole to 5 years of tamoxifen, not a test of stopping early [1, 2]. In the hormone-receptor-positive group, anastrozole reduced recurrence by about 17% over the full 5 years compared to tamoxifen (hazard ratio 0.83) [1, 2]. But that is a comparison of two different drugs, not a test of duration.
What the ATAC trial does show is that the benefit of anastrozole over tamoxifen grew over time, not that it was concentrated in the first two years [2]. The 100-month analysis found a hazard ratio of 0.81 for time to recurrence, meaning the protection continued well beyond year 2 [2]. The annual recurrence rate in years 5-10 was actually higher than in years 0-5 in one ATAC sub-study: about 2.80% per year versus 1.82% [9]. That means stopping at 2 years removes protection during a period when the risk of recurrence is still substantial.
The real-world data on discontinuation is sobering. One study found that 32% of women stopped their initial endocrine therapy within the first year, and 81% had stopped by 5 years [16]. The median time on the first drug was only 2.2 years [16]. That means many women are stopping early in practice, but the studies that track this do not report their recurrence outcomes. The question you are asking has never been answered with a randomized trial.
My call: stopping at 2 years instead of 5 means giving up a proven reduction in recurrence that continues beyond year 2, but the exact percentage increase in your personal risk is unknown because no trial tested this question. Confidence: moderate, because the indirect evidence is consistent but the direct trial is missing.
Sources used 4
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Translating trial data into patients benefits: Making the right choice
Arimidex (anastrozole) and letrozole outperform tamoxifen as initial adjuvant therapy for postmenopausal HR-positive early breast cancer, with earlier recurrence reduction and a safer overall profile, supporting AI as the preferred first-line endocrine treatment.
DOI: 10.1016/j.breast.2007.12.003 -
Review of the ATAC study: tamoxifen versus anastrozole in early-stage breast cancer
This article reviews the ATAC trial, a large randomized comparison of anastrozole, tamoxifen, and their combination in postmenopausal women with early-stage hormone receptor–positive breast cancer, showing superior disease-free and time-to-recurrence outcomes for anastrozole ver…
DOI: 10.1586/14737140.8.12.1871 -
An estrogen‐associated dietary pattern and breast cancer risk in the S wedish M ammography C ohort
This study investigates the association between an estrogen-associated dietary pattern and breast cancer risk in a cohort of 37,004 primarily postmenopausal women from the Swedish Mammography Cohort, finding that a higher estrogen dietary pattern score is linked to an increased …
DOI: 10.1002/ijc.29586 -
Early discontinuation of endocrine therapy for breast cancer: who is at risk in clinical practice?
This population-based observational study using linked health data from the NSW 45 and Up Study examines how long women with early breast cancer stay on initial versus any endocrine therapy in clinical practice, and identifies initial therapy type and comorbidity–related predict…
DOI: 10.1186/2193-1801-3-282