Clinical trial · Interventional
Anastrozole in Preventing Breast Cancer in Postmenopausal Women at Increased Risk of Breast Cancer
International Breast Cancer Intervention Study
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development of cancer. Anastrozole may be effective in preventing breast cancer. PURPOSE: This randomized clinical trial is studying how well anastrozole works in preventing breast cancer in postmenopausal women who are at increased risk for the disease.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| anastrozole | Drug | Anastrozole | ALIAS |
| placebo | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- anastrozole
- description
- anastrozole 1mg
- interventionNames
- Drug: anastrozole
- type
- PLACEBO_COMPARATOR
- label
- placebo
- description
- anastrozole 1mg PLACEBO
- interventionNames
- Drug: placebo
Primary outcomes (1)
- measure
- Development of histologically confirmed breast cancer, both invasive and non-invasive with median follow-up at 5 years
- timeFrame
- Dec 2013
Secondary outcomes (1)
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 40 Years
- Maximum age
- 70 Years
Show eligibility criteria text
DISEASE CHARACTERISTICS:
* Meets at least 1 of the relative risk factors based on age as follows:
* 45 to 70 years of age:
* First-degree relative who developed breast cancer at ≤ 50 years of age
* First-degree relative who developed bilateral breast cancer
* Two or more first- or second-degree relatives who developed breast cancer or ovarian cancer
* Participants having both relatives who are second degree and on the opposite sides of the family must have at least one that was diagnosed at ≤ 50 years of age
* Nulliparous (or first birth at ≥ 30 years of age) and a first-degree relative who developed breast cancer
* Benign biopsy with proliferative disease and a first-degree relative who developed breast cancer
* Mammographic opacity covering at least 50% of the breast in the absence of hormone replacement therapy within the past 3 months
* 60 to 70 years of age:
* First-degree relative with breast cancer at any age
* Age at menopause ≥ 55 years
* Nulliparous or age at first birth ≥ 30 years
* 40 to 44 years of age:
* Two or more first- or second-degree relatives who developed breast cancer or ovarian cancer at ≤ 50 years of age
* First-degree relative with bilateral breast cancer who developed the first breast cancer at ≤ 50 years of age
* Nulliparous (or first birth at ≥ 30 years of age) and a first-degree relative who developed breast cancer at ≤ 40 years of age
* Benign biopsy with proliferative disease and a first-degree relative who developed breast cancer at ≤ 40 years of age
* All age groups (40 to 70 ears of age) with a 10-year risk \> 5% who do not fit into the above categories are allowed
* Clearly apparent family history AND/OR other risk factors indicating appropriate increased risk of breast cancer for age
* The following prior breast conditions are allowed (for all age groups):
* Lobular carcinoma in situ
* Atypical ductal or lobular hyperplasia in a benign lesion
* Ductal carcinoma in-situ (DCIS), diagnosed within the past 6 months, and treated by mastectomy
* No evidence of breast cancer on mammogram within the past year
* Hormone receptor status:
* For patients with prior DCIS, estrogen- or progesterone-receptor status must have been positive
* Must have had greater than or equal to 5% positive cells
PATIENT CHARACTERISTICS:
Age
* 40 to 70
Sex
* Female
Menopausal status
* Postmenopausal, defined as at least 1 of the following:
* Over 60 years of age
* Bilateral oophorectomy
* ≤ 60 years of age with a uterus and amenorrhea for at least 12 months
* ≤ 60 years of age without a uterus and with follicle-stimulating hormone levels \> 30 IU/L
Performance status
* Not specified
Life expectancy
* At least 10 years
Hematopoietic
* Not specified
Hepatic
* Not specified
Renal
* Not specified
Other
* Psychologically and physically suitable to receive 5 years of anti-estrogen therapy
* No cancer within the past 5 years except non-melanoma skin cancer or carcinoma in situ of the cervix
* No evidence of osteoporosis or fragility fractures within the spine
* Participants with a T-score \> minus 4 and no more than 2 fragility fractures are allowed
* No concurrent severe disease that would place the participant at unusual risk or confound the results of the study
* No other medical condition that would preclude the ability to receive the study treatment
PRIOR CONCURRENT THERAPY:
Biologic therapy
* Not specified
Chemotherapy
* Not specified
Endocrine therapy
* No prior tamoxifen, raloxifene, or other selective estrogen receptor modulator (SERM) use for more than 6 months in duration unless an IBIS-I participant (must have been off trial therapy for at least 5 years.
* No concurrent tamoxifen, raloxifene, or other SERM
* No concurrent estrogen-based hormone replacement therapy
* No concurrent systemic estrogen replacement therapy, including vaginal estrogen preparations
Radiotherapy
* Not specified
Surgery
* See Disease Characteristics
* No prior prophylactic mastectomy
* No concurrent prophylactic mastectomy
Other
* More than 6 months since prior investigational drugsReferences
Publications (4)
- BACKGROUNDSestak I, Singh S, Cuzick J, Blake GM, Patel R, Gossiel F, Coleman R, Dowsett M, Forbes JF, Howell A, Eastell R. Changes in bone mineral density at 3 years in postmenopausal women receiving anastrozole and risedronate in the IBIS-II bone substudy: an international, double-blind, randomised, placebo-controlled trial. Lancet Oncol. 2014 Dec;15(13):1460-1468. doi: 10.1016/S1470-2045(14)71035-6. Epub 2014 Nov 11. PMID 25456365
- BACKGROUNDJenkins VA, Ambroisine LM, Atkins L, Cuzick J, Howell A, Fallowfield LJ. Effects of anastrozole on cognitive performance in postmenopausal women: a randomised, double-blind chemoprevention trial (IBIS II). Lancet Oncol. 2008 Oct;9(10):953-61. doi: 10.1016/S1470-2045(08)70207-9. Epub 2008 Sep 1. PMID 18768369
- BACKGROUNDSestak I, Smith SG, Howell A, Forbes JF, Cuzick J. Early participant-reported symptoms as predictors of adherence to anastrozole in the International Breast Cancer Intervention Studies II. Ann Oncol. 2018 Feb 1;29(2):504-509. doi: 10.1093/annonc/mdx713. PMID 29126161
- BACKGROUNDCuzick J, Sestak I, Forbes JF, Dowsett M, Knox J, Cawthorn S, Saunders C, Roche N, Mansel RE, von Minckwitz G, Bonanni B, Palva T, Howell A; IBIS-II investigators. Anastrozole for prevention of breast cancer in high-risk postmenopausal women (IBIS-II): an international, double-blind, randomised placebo-controlled trial. Lancet. 2014 Mar 22;383(9922):1041-8. doi: 10.1016/S0140-6736(13)62292-8. Epub 2013 Dec 12. PMID 24333009