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S9927 Radiation Therapy After Surgery, Chemotherapy, and/or Hormone Therapy in Stage II Breast Cancer

Randomized Trial of Post-Mastectomy Radiotherapy in Stage II Breast Cancer in Women With One to Three Positive Axillary Nodes Phase III

Status
Terminated
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00005983
Enrollment
98
Registered
2003-01-27
Start date
2000-06-30
Completion date
2005-03-31
Last updated
2013-01-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

stage II breast cancer

Brief summary

RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells. It is not yet known whether mastectomy, chemotherapy, and/or hormone therapy are more effective with or without radiation therapy in treating breast cancer. PURPOSE: Randomized phase III trial to compare the effectiveness of mastectomy, chemotherapy, and/or hormone therapy with or without radiation therapy in treating women who have stage II breast cancer.

Detailed description

OBJECTIVES: * Compare overall and disease-free survival in women with stage II breast cancer with one to three positive nodes treated with radiotherapy vs observation only after mastectomy and adjuvant chemotherapy and/or hormonal therapy. * Compare local regional control in patients treated with these regimens. * Assess the potential toxic effects of radiotherapy in this patient population. OUTLINE: This is a randomized, multicenter study. Patients are stratified according to prior systemic hormonal therapy (chemotherapy with or without hormonal therapy vs hormonal therapy alone), prior taxane exposure (yes vs no), and duration of chemotherapy (no chemotherapy vs less than 3 months vs 3-5 months vs 6 months or more). Patients are randomized to one of two treatment arms. * Arm I: Patients undergo radiotherapy 5 days a week for 5 weeks. * Arm II: Patients are observed for disease progression. Patients are followed every 6 months for 2 years and then annually for 15 years. PROJECTED ACCRUAL: A total of 2,500 patients (1,250 per treatment arm) will be accrued for this study within 5 years.

Interventions

RADIATIONradiation therapy
PROCEDUREsurgery

surgery

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
North Central Cancer Treatment Group
CollaboratorNETWORK
American College of Surgeons
CollaboratorOTHER
Eastern Cooperative Oncology Group
CollaboratorNETWORK
Radiation Therapy Oncology Group
CollaboratorNETWORK
Cancer and Leukemia Group B
CollaboratorNETWORK
NCIC Clinical Trials Group
CollaboratorNETWORK
NSABP Foundation Inc
CollaboratorNETWORK
SWOG Cancer Research Network
Lead SponsorNETWORK

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
21 Years to No maximum
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Histologically confirmed stage II adenocarcinoma of the breast (T1-2, N1, M0) * Primary tumor no greater than 5 cm * At least 1 but no more than 3 positive axillary lymph nodes * Nodes cannot be positive solely by cytokeratin staining * No apocrine, adenocystic, or squamous cell carcinomas or sarcomas of the breast * No bilateral breast cancer * No active local regional disease * Must have undergone a modified radical mastectomy with a level I and II with or without a level III axillary dissection (at least 10 nodes examined) within the past 8 months * Surgical margins negative for invasive and noninvasive ductal carcinoma * No gross extracapsular disease or residual disease in the axilla * Microscopic extracapsular extension allowed * No mastectomy after local failure following lumpectomy * Must have received adjuvant chemotherapy and/or hormonal therapy after mastectomy * Hormone receptor status: * Not specified PATIENT CHARACTERISTICS: Age: * 21 and over Sex: * Female Menopausal status: * Pre- or post-menopausal Performance status: * Zubrod 0-1 Life expectancy: * Not specified Hematopoietic: * Not specified Hepatic: * Not specified Renal: * Not specified Other: * Not pregnant or nursing * Fertile patients must use effective contraception * No other prior malignancy within the past 5 years except adequately treated basal cell or squamous cell skin cancer or carcinoma in situ of the cervix * No serious medical or psychiatric illness that would preclude study compliance PRIOR CONCURRENT THERAPY: Biologic therapy: * No prior trastuzumab (Herceptin) Chemotherapy: * See Disease Characteristics * No more than 6 weeks since prior adjuvant chemotherapy * No other prior chemotherapy * Concurrent adjuvant chemotherapy allowed Endocrine therapy: * See Disease Characteristics * Concurrent adjuvant hormonal therapy allowed Radiotherapy: * No prior chest wall or nodal radiotherapy Surgery: * See Disease Characteristics * Breast reconstruction allowed Other: * Concurrent registration on another adjuvant chemotherapy or hormonal therapy study is allowed

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026