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.

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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.

View Eligibility Criteria

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

Study is for people with:

Breast Cancer

Phase:

Phase 3

Estimated Enrollment:

86

Study ID:

NCT00659373

Recruitment Status:

Completed

Sponsor:

ETOP IBCSG Partners Foundation

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There are 13 Locations for this study

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Mercy General Hospital
Sacramento California, 95819, United States
Front Range Cancer Specialists
Fort Collins Colorado, 80528, United States
Norwalk Hospital
Norwalk Connecticut, 06856, United States
Piedmont Hospital
Atlanta Georgia, 30309, United States
Northside Hospital Cancer Center
Atlanta Georgia, 30342, United States
Saint Joseph's Hospital of Atlanta
Atlanta Georgia, 30342, United States
CCOP - Atlanta Regional
Atlanta Georgia, 30342, United States
CCOP - Northern Indiana CR Consortium
South Bend Indiana, 46601, United States
New Hampshire Oncology - Hematology, PA at Payson Center for Cancer Care
Concord New Hampshire, 03301, United States
Don Monti Comprehensive Cancer Center at North Shore University Hospital
Manhasset New York, 11030, United States
Mission Hospitals - Memorial Campus
Asheville North Carolina, 28801, United States
Batte Cancer Center at Northeast Medical Center
Concord North Carolina, 28025, United States
Abramson Cancer Center of the University of Pennsylvania
Philadelphia Pennsylvania, 19104, United States
British Columbia Cancer Agency - Centre for the Southern Interior
Kelowna British Columbia, V1Y 5, Canada
Ottawa Hospital Regional Cancer Centre - General Campus
Ottawa Ontario, K1H 1, Canada

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 3

Estimated Enrollment:

86

Study ID:

NCT00659373

Recruitment Status:

Completed

Sponsor:


ETOP IBCSG Partners Foundation

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