Clinical trial · Interventional
Effect of Bisphosphonate on Bone Loss in Postmenopausal Women With Breast Cancer Initiating Aromatase Inhibitor Therapy
The Effect of Bisphosphonate on Bone Mass and Bone Turnover in Elderly, Postmenopausal Women With Breast Cancer Following Initiation of Aromatase Inhibitor Therapy
- 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)
Elderly, postmenopausal women with breast cancer on aromatase inhibitors are at increased risk of developing bone loss and osteoporosis. We postulate that in elderly, osteopenic postmenopausal women who are on aromatase inhibitor therapy, bisphosphonate therapy will (1) prevent bone loss at clinically relevant sites, such as the spine and hip and (2) decrease bone turnover.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Bone Loss | — | UNRESOLVED | — |
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Osteoporosis | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| risedronate | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Active Medication Group
- description
- risedronate 35 mg weekly
- interventionNames
- Drug: risedronate
- type
- NO_INTERVENTION
- label
- Placebo Group
- description
- Placebo
Primary outcomes (1)
- measure
- BMD of Spine by DXA
- timeFrame
- at 24 months
- description
- BMD is the bone mineral density of the lumbar spine measured using the dual-energy x-ray absorptometry (DXA) scan.
Secondary outcomes (2)
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 55 Years
Show eligibility criteria text
Inclusion Criteria: * elderly postmenopausal women (ages 55 and older) * osteopenic (DXA T-score -1.0 to -2.5 SD). However, after full counseling about the risks, benefits, and options regarding therapy for osteoporosis and discussion with her PCP, an osteoporotic woman may enroll in the study. * with breast cancer on aromatase inhibitor therapy * with no evidence of distant metastatic disease or osteoporosis (by BMD or clinical history) * type of surgical procedure or addition of radiation therapy prior to this aromatase inhibitor therapy will not exclude patients * Participants must provide voluntary, written informed consent to participate in the study, which includes understanding of the procedures, medications, and risks and benefits Exclusion Criteria: * Women with stage 4 breast cancer (presence of distant metastases) * Women with normal bone density by DXA (T-score \> -1.0 SD)bone density by DXA, except in the instance of a fragility fracture. * Women with history of any illness known to affect bone and mineral metabolism, such as renal failure (estimated GFR \<30), hepatic failure, malignancy (excluding breast cancer, treated superficial basal and squamous cell carcinoma and malignancies where the diagnosis itself or its treatment would not adversely affect bone metabolism), untreated primary hyperparathyroidism, and malabsorption. * Women being treated with oral glucocorticoid therapy \>3 months for suppression therapy, and certain anti-seizure medications which may adversely affect bone metabolism (phenobarbital, phenytoin, carbamazepine). * Those with untreated active peptic ulcer disease * Those with osteoporosis by BMD (T-score -2.5 SD at the spine or total hip) or a history of fragility fracture as an adult. However, as discussed above, osteoporotic women may elect to enroll in the study. * Women treated with oral bisphosphonates or calcitonin for 3 months within the last year (3 month washout period) * Men and children will be excluded because they do not get postmenopausal osteoporosis following treatment with an aromatase inhibitor * Women with very poor dental hygiene (as assessed by the baseline dental exam) in need of dental extraction during the study * Use of fluoride for more than 1 month ever (except for dental treatment) * Less than 2 evaluable vertebrae * Distant metastatic disease
References
Publications (1)
- DERIVEDAdams A, Jakob T, Huth A, Monsef I, Ernst M, Kopp M, Caro-Valenzuela J, Wockel A, Skoetz N. Bone-modifying agents for reducing bone loss in women with early and locally advanced breast cancer: a network meta-analysis. Cochrane Database Syst Rev. 2024 Jul 9;7(7):CD013451. doi: 10.1002/14651858.CD013451.pub2. PMID 38979716