Breast Cancer
Conditions
Keywords
stage II breast cancer, stage IIIA breast cancer, stage IIIB breast cancer, inflammatory breast cancer
Brief summary
RATIONALE: Breast-conserving treatments such as radiation therapy or limited surgery are less invasive than mastectomy and may improve the quality of life. It is not yet known if breast-conserving treatments are as effective as mastectomy followed by radiation therapy in treating locally advanced breast cancer. PURPOSE: Randomized phase III trial to compare the effectiveness of breast-conserving therapy with mastectomy followed by radiation therapy in treating women who have locally advanced breast cancer that has been previously treated with chemotherapy.
Detailed description
OBJECTIVES: * Compare the overall survival and time to loco-regional failure in women with locally advanced breast cancer treated with breast-conserving local therapy vs mastectomy followed by radiotherapy after they have received prior induction chemotherapy. * Compare the quality of life of patients treated with these regimens. OUTLINE: This is a randomized, multicenter study. Patients are stratified according to participating center, initial stage (T0, T1, T2, T3, or Tx vs T4), response to prior induction chemotherapy (complete response (CR) vs other), and menopausal status (premenopausal vs postmenopausal). Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients undergo mastectomy followed by radiotherapy. * Arm II: Patients receive breast-conserving treatment comprising 1 of 3 of the following therapeutic options: * Regimen A: Patients receive radiotherapy alone. * Regimen B: Patients with a partial response (PR) to prior induction chemotherapy undergo limited surgery followed by radiotherapy. Patients with a CR to prior induction chemotherapy undergo radiotherapy alone. * Regimen C: Patients with a partial response (PR) or CR to prior induction chemotherapy undergo radiotherapy alone. Patients with a CR to radiotherapy receive no further treatment. Patients with a PR to radiotherapy undergo limited surgery. Quality of life is assessed at baseline, at the end of therapy, every 3 months for 2 years, every 6 months for 3 years, and then annually thereafter. Patients are followed within 1 month, every 3 months for 2 years, every 6 months for 3 years, and then annually thereafter. PROJECTED ACCRUAL: A total of 1,300 patients (650 per treatment arm) will be accrued for this study within 5 years.
Interventions
PROCEDUREconventional surgery
RADIATIONradiation therapy
Sponsors
Central and Eastern European Oncology Group
Grupo Oncologico Cooperativo Chileno de Investigation
International Collaborative Cancer Group
European Organisation for Research and Treatment of Cancer - EORTC
Study design
Allocation
RANDOMIZED
Primary purpose
TREATMENT
Eligibility
Sex/Gender
FEMALE
Healthy volunteers
No
Inclusion criteria
DISEASE CHARACTERISTICS: * Histologically or cytologically confirmed locally advanced breast cancer * T3 inoperable, N0-N2 * Any T, N2 * T4, N0-N2 * Inflammatory breast carcinoma * Prior treatment with 4-6 courses of standard induction chemotherapy or active investigational regimens completed within the past 4 weeks * Residual tumor size less than 5 cm * No fixed axillary lymph nodes * No multifocal or bilateral breast cancer * No clinical suspicion of extensive ductal carcinoma in situ * No unresolved skin edema * No distant metastases (including ipsilateral supraclavicular node) * Positive bone scan allowed provided there are no bone metastases on x-ray * Hormone receptor status: * Not specified PATIENT CHARACTERISTICS: Age: * Any age Sex: * Female Menopausal status: * Not specified Performance status: * WHO 0-1 Life expectancy: * Not specified Hematopoietic: * Neutrophil count at least 2,000/mm\^3 * Platelet count at least 100,000/mm\^3 Hepatic: * Bilirubin less than 1.5 times normal * SGOT and SGPT no greater than 2 times normal * Alkaline phosphatase no greater than 2 times normal Renal: * Creatinine less than 1.5 times normal Other: * No other prior or concurrent malignancy except adequately treated squamous cell or basal cell skin cancer or adequately treated cone-biopsied carcinoma in situ of the cervix * No serious underlying medical illness that would preclude study * No psychiatric or addictive disorder that would preclude study * No contraindication to study treatment * Not pregnant * Fertile patients must use effective barrier contraception PRIOR CONCURRENT THERAPY: Biologic therapy: * Not specified Chemotherapy: * See Disease Characteristics Endocrine therapy: * No concurrent hormonal replacement therapy * No concurrent oral contraceptives Radiotherapy: * See Disease Characteristics * No prior radiotherapy for breast cancer Surgery: * No prior surgery for breast cancer other than biopsy for diagnosis confirmation Other: * No other prior systemic therapy for breast cancer
Countries
Belgium, Chile, Israel, Netherlands, Poland, Portugal, United Kingdom
Outcome results
None listed