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N/A N=115

Loss of Grip Strength, BMI, and Adjuvant Endocrine Therapy Breast Cancer

Breast Cancer · Arthralgia · Obesity

Enrolled (actual)
115
Serious AEs
0.9%
Results posted
May 2016
Primary outcome: Primary: Effect of Change in Body Mass Index on Change in Grip Strength With Aromatase Inhibitor Therapy — -0.15; 2.44 kg/m^2 — p=0.03

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
anastrozole, letrozole, exemestane (Drug); Tamoxifen (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
Female
Sponsor
University of Michigan Rogel Cancer Center
Primary completion
Aug 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Effect of Change in Body Mass Index on Change in Grip Strength With Aromatase Inhibitor Therapy
-0.15; 2.44 0.03 sig
SECONDARY
Effect of Medication on Change in Grip Strength
-7.0; 0.6 0.032 sig
SECONDARY
Association Between Baseline Body Mass Index and Discontinuation of Aromatase Inhibitor Therapy Within the First 12 Months
37; 2

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. Initial reports suggest that grip strength decreases during aromatase inhibitor therapy, and that body-mass index may influence development of this symptom. Therefore, this longitudinal study has been developed to determine change in grip strength over time in women treated with aromatase inhibitors and tamoxifen, as well as to identify potential associations between change in grip strength and BMI. Patient self-reported symptoms will also be collected. A total of 115 women with early stage breast cancer who are initiating therapy with either an aromatase inhibitor or tamoxifen will be enrolled.

Eligibility Criteria

Inclusion Criteria

  • Stage 0-III breast cancer who are scheduled to receive endocrine therapy with tamoxifen or an aromatase inhibitor
  • All prior surgery and chemotherapy should be complete
  • Age 18 and above and postmenopausal

Exclusion Criteria

  • Major rheumatologic disorders
  • Concomitant sex hormone containing drugs or Leutinizing Hormone Releasing Hormone agonist therapy
  • For those subjects initiating treatment with an aromatase inhibitor, prior tamoxifen within 4 weeks of enrollment
  • For those subjects initiating treatment with tamoxifen, prior aromatase inhibitor within 4 weeks of enrollment
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01896050). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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