Overview

NSAID Effects on Clinical and Imaging Breast Biomarkers

Status:
Unknown status
Trial end date:
2019-06-01
Target enrollment:
0
Participant gender:
Female
Summary
This study has two purposes. One is to determine if daily sulindac decreases breast density; a risk factor for breast cancer development. The second is to determine whether sulindac reduces pain and stiffness associated with regular use of aromatase inhibitors given for the treatment of breast cancer.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Stony Brook University
Treatments:
Aromatase Inhibitors
Sulindac
Criteria
Inclusion Criteria:

- Eligibility criteria will include: Postmenopausal women with of first incidence of
early stage (stages 0 - III) hormone receptor positive breast cancer stabilized on
anastrozole therapy for at least 3 months

- Patients must have started on anastrozole and plan to continue on anastrozole therapy
for a minimum of 12 months

- Patients must have an unaffected, non-irradiated contralateral breast with a baseline
breast density score of > 25% as measured by standard digital mammography (BIRADs
score > 2) or magnetic resonance imaging (MRI) performed within 12 months of
randomization to the study

- A willingness to follow the study protocol, as indicated by provision of informed
consent to participate

- A willingness to avoid taking NSAIDs outside of the trial (rare NSAID use for
musculoskeletal symptoms excepted)

- Normal renal function as determined by a serum creatinine < upper limit of normal

- No known contraindication to NSAID use

- Normotensive or controlled blood pressure (< 140/90) on a single anti-hypertensive
medication

Exclusion Criteria:

- Current or anticipated need for daily aspirin or NSAID use including aspirin for
cardiovascular protection

- Known intolerance to NSAIDs

- Age > 75 years

- History of cardiovascular disease including prior myocardial infarction, angina,
stroke, or transient ischemic attack (TIA)

- Diabetes requiring drug therapy

- Current smoker

- History of Uncontrolled hypertension

- Blood pressure > 140/90 at baseline by home monitoring

- History of GI ulcers, chronic GERD, or GI bleeding in the past 5 years

- History of a bleeding diathesis or current anticoagulant therapy

- Daily therapy with H2 blockers or protein pump inhibitors

- History of claustrophobia

- Have electrically, magnetically, or mechanically activated implants including cardiac
pacemaker, cochlear implants, magnetic surgical clips or prostheses.