Status:

COMPLETED

Quality of Life in Postmenopausal Women Who Are Receiving Either Exemestane or Anastrozole With or Without Celecoxib for Stage I, Stage II, or Stage IIIA Primary Breast Cancer

Lead Sponsor:

Eastern Cooperative Oncology Group

Collaborating Sponsors:

National Cancer Institute (NCI)

NCIC Clinical Trials Group

Conditions:

Breast Cancer

Eligibility:

FEMALE

Up to 120 years

Brief Summary

RATIONALE: Quality-of-life assessment in postmenopausal women who are receiving hormone therapy for breast cancer may help to determine the effects of treatment on these patients and may improve the q...

Detailed Description

OBJECTIVES: Primary * Compare treatment-related symptoms using the Functional Assessment of Cancer Therapy-Endocrine Symptoms (FACT-ES) questionnaire in postmenopausal women with receptor-positive s...

Eligibility Criteria

Inclusion

  • DISEASE CHARACTERISTICS:
  • Histologically confirmed invasive breast cancer
  • pT1-3; pNX, pN0-2 or pN3\*; M0 NOTE: \*Only when the sole basis for this classification is the presence of 10 or more involved axillary lymph nodes
  • Registered on protocol CAN-NCIC-MA27 within the past week
  • Hormone receptor status:
  • Estrogen receptor- and/or progesterone receptor-positive by immunohistochemistry or tumor receptor content ≥ 10 fmol/mg protein
  • At least 1 tumor must be receptor-positive in patients with bilateral breast cancer
  • PATIENT CHARACTERISTICS:
  • Age
  • Postmenopausal
  • Performance status
  • ECOG 0-2
  • Sex
  • Female
  • Menopausal status
  • Postmenopausal
  • Life expectancy
  • Not specified
  • Hematopoietic
  • Not specified
  • Hepatic
  • Not specified
  • Renal
  • Not specified
  • Other
  • Able to read, understand, and complete quality of life questionnaires
  • PRIOR CONCURRENT THERAPY:
  • Biologic therapy
  • Not specified
  • Chemotherapy
  • Not specified
  • Endocrine therapy
  • Not specified
  • Radiotherapy
  • Not specified
  • Surgery
  • Not specified

Exclusion

    Key Trial Info

    Start Date :

    January 26 2005

    Trial Type :

    OBSERVATIONAL

    End Date :

    January 30 2013

    Estimated Enrollment :

    Patients enrolled

    Trial Details

    Trial ID

    NCT00090974

    Start Date

    January 26 2005

    End Date

    January 30 2013

    Last Update

    June 15 2023

    Active Locations (224)

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    Page 1 of 56 (224 locations)

    1

    Fairbanks Cancer Treatment Center at Fairbanks Memorial Hospital

    Fairbanks, Alaska, United States, 99701

    2

    Banner Good Samaritan Medical Center

    Phoenix, Arizona, United States, 85006

    3

    CCOP - Western Regional, Arizona

    Phoenix, Arizona, United States, 85006

    4

    Banner Thunderbird Medical Center

    Phoenix, Arizona, United States, 85306