Overview

Hormone Therapy and Chemotherapy in Treating Perimenopausal or Postmenopausal Women With Node-Positive Breast Cancer

Status:
Completed
Trial end date:
2010-08-01
Target enrollment:
0
Participant gender:
Female
Summary
RATIONALE: Estrogen can stimulate the growth of breast cancer cells. Hormone therapy may fight breast cancer by blocking the uptake of estrogen. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining chemotherapy with hormone therapy may kill more tumor cells. It is not yet known which treatment regimen is more effective for breast cancer. PURPOSE: Randomized phase III trial to compare the effectiveness of hormone therapy during or after combination chemotherapy or hormone therapy alone in treating perimenopausal or postmenopausal women who have stage II or stage IIIA breast cancer.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
International Breast Cancer Study Group
Treatments:
Cyclophosphamide
Doxorubicin
Epirubicin
Liposomal doxorubicin
Tamoxifen
Toremifene
Criteria
DISEASE CHARACTERISTICS: Histologically proven stage T1-3, pN1, M0 carcinoma of the breast
considered suitable for adjuvant treatment with endocrine therapy alone Estrogen receptor
at least 10 fmol/mg cytosol protein or positive on immunohistochemical assay Potentially
curative resection within 6 weeks of entry by one of the following: Total mastectomy with
negative margins Breast-conserving procedure (lumpectomy or quadrantectomy) for tumors less
than 5 cm Adequate re-resection or mastectomy within 4 weeks of initial surgery required if
margins are positive after initial surgery Axillary clearance (not sampling) required at
surgery, with at least 1 node positive upon histopathologic examination of at least 8 nodes
Suspicious manifestations of metastatic disease (e.g., hot spots on bone scan, skeletal
pain of unknown cause) must be proven benign No bilateral breast cancer Any mass in
contralateral breast must be proven benign by biopsy

PATIENT CHARACTERISTICS: Age: 70 and under Sex: Women only Menopausal status:
Peri/postmenopausal, i.e.: More than 6 months since last normal menstrual period (LNMP)
with no prior hysterectomy and no hormone replacement therapy (HRT) Prior hysterectomy and
no HRT and either age greater than 55 or age 55 or less with postmenopausal LH, FSH, and E2
levels On HRT and either age 50 or greater or LNMP more than 6 months prior to starting HRT
Performance status: Not specified Hematopoietic: WBC greater than 4,000 Platelets greater
than 100,000 Hepatic: Bilirubin less than 1.1 mg/dL (20 micromoles/L) AST less than 60 IU/L
Renal: Creatinine less than 1.3 mg/dL (120 micromoles/L) Other: No nonmalignant systemic
disease that would preclude protocol therapy or prolonged follow-up No psychiatric or
addictive disorder that would preclude informed consent No prior or concurrent second
malignancy except: Nonmelanomatous skin cancer Adequately treated in situ carcinoma of the
cervix Geographically accessible for follow-up

PRIOR CONCURRENT THERAPY: No prior therapy for breast cancer other than potentially
curative surgery (see Disease Characteristics)