Breast Cancer
Conditions
Keywords
stage IA breast cancer, stage IB breast cancer, stage II breast cancer
Brief summary
RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells and may be a less invasive treatment and cause fewer side effects than complete axillary lymph node dissection. It is not yet known which treatment is more effective for invasive breast cancer. PURPOSE: Randomized phase III trial to compare the effectiveness of complete axillary lymph node dissection with that of axillary radiation therapy in treating women who have invasive breast cancer.
Detailed description
OBJECTIVES: * Compare the regional control of the axilla obtained by complete axillary lymph node dissection vs axillary radiotherapy in sentinel lymph node-positive women with operable invasive breast cancer. * Determine whether local and regional axillary control can be obtained without axillary lymph node dissection in sentinel lymph node-negative women. * Compare the axillary 5-year recurrence-free survival of these patients treated with these regimens. * Compare the morbidity of patients treated with these regimens. * Compare the quality of life of these patients treated with these regimens. OUTLINE: This is a randomized, multicenter study. Patients are stratified according to participating center and type of breast surgery (conservation vs total mastectomy). Patients are randomized to 1 of 2 treatment arms. Patients are given an injection of a tracer and undergo lymphoscintigraphy 2-3 hours later to identify the sentinel lymph node. Within 24 hours after lymphoscintigraphy, patients undergo wide local excision of the tumor or mastectomy after the sentinel node is removed. If no sentinel node is found or metastasis is found in a nonsentinel node, patients undergo complete axillary lymph node dissection (ALND) regardless of randomization. Sentinel node-negative patients receive no further treatment. Sentinel node-positive patients continue treatment according to randomization. * Arm I: Within 8 weeks after surgery, patients undergo complete ALND. * Arm II: Within 8 weeks after surgery, patients undergo axillary lymph node radiotherapy daily 5 days a week for 5 weeks. Patients in arm I may receive postoperative axillary irradiation if 4 or more nodes are positive and more than 1 axillary level is involved. Quality of life is assessed at baseline and then at 1, 2, 3, and 5 years. Patients are followed annually for 5 years. PROJECTED ACCRUAL: A total of 3,485 patients (1,394 sentinel node-positive and 2,091 sentinel node-negative) will be accrued for this study within 3 years.
Interventions
PROCEDUREaxillary lymph node dissection
PROCEDURElymphoscintigraphy
PROCEDUREtherapeutic conventional surgery
RADIATIONradiation therapy
Sponsors
ALMANAC Trialists Group
Borstkanker Onderzoeksgroup Nederland
European Organisation for Research and Treatment of Cancer - EORTC
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Healthy volunteers
No
Inclusion criteria
DISEASE CHARACTERISTICS: * Histologically or triple diagnosis (palpation, mammogram or ultrasound, and cytology) confirmed operable invasive breast cancer * T0-2, N0 * Diagnosis by excisional tumorectomy allowed * Clinically occult invasive disease must be histologically confirmed * Only 1 tumor in 1 breast * Tumor between 5 and 50 mm in largest diameter, within 1 quadrant by mammogram, ultrasound or MRI * Multifocal (i.e., within one quadrant and sharing the same histological characteristics) is allowed * Multicentric (i.e., in different quadrants) breast cancer is not allowed * Clinically negative axillary lymph nodes * No metastatic disease * No previous treatment of the primary breast tumor by neoadjuvant hormonal or systemic treatment * Hormone receptor status: * Not specified PATIENT CHARACTERISTICS: Age: * Any age Sex: * Female Menopausal status: * Not specified Performance status: * Not specified Life expectancy: * Not specified Hematopoietic: * Not specified Hepatic: * Not specified Renal: * Not specified Other: * Fit to undergo sentinel node biopsy, axillary clearance, breast surgery, and/or axillary radiotherapy * No psychological, familial, sociological, or geographical condition that would preclude study compliance * No other prior malignancy except basal cell skin cancer or carcinoma in situ of the cervix * Not pregnant PRIOR CONCURRENT THERAPY: Biologic therapy: * Not specified Chemotherapy: * Not specified Endocrine therapy: * Not specified Radiotherapy: * No prior radiotherapy to axilla Surgery: * No prior surgery to axilla Other: * See Disease Characteristics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Axillary recurrence rate | from randomization |
Secondary
| Measure | Time frame |
|---|---|
| Shoulder function as assessed by arm function test questionnaire at baseline, 1, 3, and 5 years after surgery | from randomization |
| Quality of life as measured by Quality of Life Questionnaire Core 30 Items (QLQ-C30) and QLQ-BR25 at baseline, 1, 2, 3, and 5 years after surgery | from randomization |
| Axillary recurrence-free survival | from randomization |
| Disease-free survival | from randomization |
| Overall survival | from randomization |
Countries
France, Italy, Netherlands, Poland, Slovenia, Switzerland, Turkey (Türkiye), United Kingdom
Outcome results
None listed