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Clinical Trials/NCT02118636
NCT02118636
Completed
Not Applicable

Prospective Observational Study of Breast Cancer Patients Starting Therapy With an AI to Evaluate Mechanisms Underlying Development of Aromatase Inhibitor Associated Musculoskeletal Symptoms

Lynn Henry1 site in 1 country75 target enrollmentOctober 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Breast Cancer
Sponsor
Lynn Henry
Enrollment
75
Locations
1
Primary Endpoint
Change in estradiol and development of musculoskeletal symptoms between baseline and 3 months
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Early stage hormone receptor positive breast cancer is typically treated with adjuvant endocrine therapy in order to decrease risk of breast cancer recurrence and to improve overall survival from the disease. Typical agents used for treatment include tamoxifen and the aromatase inhibitors. In postmenopausal women, aromatase inhibitor therapy is increasingly common because it is associated with fewer long-term serious toxicities compared to tamoxifen. However, aromatase inhibitors cause arthralgias in 40-50% of patients, which can influence adherence to therapy and can lead to treatment discontinuation in a minority of cases. The mechanism underlying development of this toxicity remains unclear, and predictors of who will develop these symptoms remain undefined. This observational study is designed to collect patient-reported outcomes and serial serum samples in order to investigate potential etiologies of this bothersome toxicity.

Registry
clinicaltrials.gov
Start Date
October 2009
End Date
September 2015
Last Updated
10 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Lynn Henry
Responsible Party
Sponsor Investigator
Principal Investigator

Lynn Henry

Assistant Professor

University of Michigan Rogel Cancer Center

Eligibility Criteria

Inclusion Criteria

  • Stage I-III breast cancer who are scheduled to receive endocrine therapy with an aromatase inhibitor
  • All prior surgery, chemotherapy, and radiation therapy should be complete or should be completed by the time of AI treatment initiation (within 28 days of study enrollment)
  • Age 21 and above and postmenopausal

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Change in estradiol and development of musculoskeletal symptoms between baseline and 3 months

Time Frame: 12 months

To identify associations between estradiol serum concentrations at baseline and after 3 months of aromatase inhibitor therapy and the development of aromatase inhibitor-associated musculoskeletal symptoms by 12 months

Secondary Outcomes

  • Change in sex hormones and development of musculoskeletal symptoms between baseline and 3 months(12 months)

Study Sites (1)

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