OpenNeedle Ask your own

Question explored with the scientific record

Conversation so far

  1. 1 can anastrazole be stopped after 2 years
  2. 2 How much higher is my recurrence risk if I stop after 2 years?

Answered on this page ↓

How much higher is my recurrence risk if I stop after 2 years?

Sep 7, 2026 · 5 sources used · OpenNeedle synthesis
The short version: no trial has ever randomly assigned women to stop anastrozole at 2 years versus continue to 5 years, so the exact number you are asking for does not exist in the evidence.

The closest data comes from the ATAC trial, which compared 5 years of anastrozole to 5 years of tamoxifen in over 9,000 women [1, 2]. In the hormone-receptor-positive group, anastrozole reduced recurrence by about 17% compared to tamoxifen over the full 5 years (hazard ratio 0.83) [1, 2]. But that is a comparison of two different drugs, not a test of stopping early. The DATA trial tested 6 years versus 3 years of anastrozole after initial tamoxifen and found a hazard ratio of 0.79 for disease-free survival, but the result did not reach statistical significance (p=0.066) [13]. That means even the benefit of going from 3 to 6 years was uncertain in that study.

What the evidence does show is that recurrence risk in hormone-receptor-positive breast cancer does not front-load in the first two years. The ATAC trial's 100-month analysis showed the benefit of anastrozole over tamoxifen grew over time, not that it was concentrated early [2]. The annual recurrence rate in years 5-10 was actually higher than in years 0-5 in one ATAC sub-study: 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 2025 retrospective Mexican study of 301 patients found that longer therapy duration consistently reduced recurrence, with an odds ratio of 0.18 for therapy beyond 36 months versus less than 36 months [11]. That is a large effect, but it is observational, not randomized, and the confidence intervals are wide.

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. The evidence suggests the increase is real and may be substantial, especially if your tumor was high-risk. Confidence: moderate, because the direct trial is missing but the indirect evidence is consistent.

Keep digging

Sources used 5

  1. Translating trial data into patients benefits: Making the right choice The Breast (2008) Thin

    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
  2. Review of the ATAC study: tamoxifen versus anastrozole in early-stage breast cancer Expert Review of Anticancer Therapy (2008) Thin

    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
  3. Estrogen Receptor Expression in 21-Gene Recurrence Score Predicts Increased Late Recurrence for Estrogen-Positive/HER2-Negative Breast Cancer Clinical Cancer Research (2015) Thin

    A retrospective analysis of the ATAC trial showing that individual genes and gene modules within the 21-gene recurrence score interact with time to differently predict recurrence in estrogen receptor–positive, HER2-negative breast cancer treated with tamoxifen or anastrozole, wi…

    DOI: 10.1158/1078-0432.ccr-14-2842
  4. Effect of adjuvant endocrine therapy: single-agent vs. switching on breast cancer-free and overall survival-a retrospective cohort study Reports of Practical Oncology and Radiotherapy (2025) Thin

    A retrospective cohort study of hormone receptor–positive breast cancer in Mexican patients comparing single-agent adjuvant endocrine therapy (tamoxifen or aromatase inhibitor) versus switching between agents, assessing breast cancer–free survival and overall survival over up to…

    DOI: 10.5603/rpor.107761
  5. Extended adjuvant aromatase inhibition after sequential endocrine therapy (DATA): a randomised, phase 3 trial The Lancet Oncology (2017) Thin

    The DATA study, a phase 3 trial, investigates the efficacy of extended anastrozole therapy after sequential tamoxifen treatment in postmenopausal women with hormone receptor-positive breast cancer, finding no significant improvement in disease-free survival with 6 years of anast…

    DOI: 10.1016/S1470-2045(17)30600-9

Your question next

What do you want to know?

No question is too uncomfortable for the evidence. Bring yours.

Ask your question