Breast Cancer Clinical Trial
Brain Function in Premenopausal Women Receiving Tamoxifen With or Without Ovarian Function Suppression for Early-Stage Breast Cancer on Clinical Trial IBCSG 24-02
Summary
RATIONALE: Learning about the long-term effects of adjuvant tamoxifen (T), adjuvant tamoxifen with ovarian function suppression (T+OFS), and exemestane with ovarian function suppression (E+ OFS) on brain function may help doctors plan cancer treatment.
PURPOSE: This study is looking at brain function in premenopausal women who are receiving adjuvant tamoxifen (T) alone against those receive adjuvant tamoxifen (T+OFS) or exemestane (E+OFS) with ovarian function suppression (OFS) for early-stage breast cancer on clinical trial IBCSG-2402.
Full Description
OBJECTIVES:
Primary:
* To evaluate and compare the changes in cognitive function over one year in premenopausal breast cancer patients who receive adjuvant tamoxifen (T) alone against those receive adjuvant tamoxifen (T+OFS) or exemestane (E+OFS) with ovarian function suppression (OFS).
OUTLINE: This is a multicenter study.
Objective cognitive function was measured with the CogState computerized test battery. The CogState battery consists of seven tasks: Detection, Identification, Monitoring, Memory, Learning, International Shopping List Task (ISLT), and ISLT-Delayed Recall. Performance speed is measured for the Detection, Identification and Monitoring tasks and performance accuracy is measured for the Memory, Learning, ISLT, and ISLT-Delayed Recall. Measures of performance speed are normalized using measures of performance accuracy (%) are normalized using arcsine transformation. The main outcome measure is a composite score which is the average of these task scores (after transformation and standardization by age-specific norms). Patients complete these assessments at baseline (i.e. before start of protocol hormonal therapy) and approximately one year after randomization to the parent IBCSG 24-02 (SOFT) study.
Data were collected separately for the T+OFS and E+OFS participants in the parent study, IBCSG 24-02 (SOFT). The sample size for this Co-SOFT substudy was small, so the analysis plan was revised to pre-specify collective analysis for all patients receiving OFS.
Eligibility Criteria
DISEASE CHARACTERISTICS:
Histologically confirmed breast cancer
Completely resected disease
Registered for clinical trial IBCSG-2402, but not yet started protocol hormonal therapy
Has not yet received any of the following adjuvant endocrine therapy, either before or after registration on IBCSG-2402:
Tamoxifen, exemestane, or gonadotropin-releasing hormone (GnRH) agonist
Ovarian irradiation
Bilateral oophorectomy
Hormone receptor status:
Estrogen and/or progesterone receptor positive
Each tumor must be hormone receptor positive
PATIENT CHARACTERISTICS:
Premenopausal
Can speak and read the local language(s) fluently
PRIOR CONCURRENT THERAPY:
See Disease Characteristics
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There are 13 Locations for this study
Sacramento California, 95819, United States
Fort Collins Colorado, 80528, United States
Norwalk Connecticut, 06856, United States
Atlanta Georgia, 30309, United States
Atlanta Georgia, 30342, United States
Atlanta Georgia, 30342, United States
Atlanta Georgia, 30342, United States
South Bend Indiana, 46601, United States
Concord New Hampshire, 03301, United States
Manhasset New York, 11030, United States
Asheville North Carolina, 28801, United States
Concord North Carolina, 28025, United States
Philadelphia Pennsylvania, 19104, United States
Kelowna British Columbia, V1Y 5, Canada
Ottawa Ontario, K1H 1, Canada
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