Radiation Therapy in Treating Women Undergoing Lumpectomy for Stage I or Stage IIA Breast Cancer

Mayo Clinic

Status and phase: Completed; Phase 2

Conditions: Breast Cancer

Treatments: Procedure: conventional surgery; Radiation: hypofractionated radiation therapy; Procedure: adjuvant therapy; Radiation: intraoperative radiation therapy

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT00602108

P30CA015083 (U.S. NIH Grant/Contract)

CDR0000583007

806-04 (Other Identifier)

MCS314 (Other Identifier)

Details and patient eligibility

About

RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. Giving intraoperative radiation therapy after lumpectomy followed by external-beam radiation therapy may kill any tumor cells that remain after surgery.

PURPOSE: This phase II trial is studying the side effects and how well radiation therapy works in treating women undergoing lumpectomy for stage I or stage IIA breast cancer.

Full description

OBJECTIVES:

• To determine the feasibility and acute patient tolerance of intraoperative electron irradiation (IOERT) and hypofractionated external-beam irradiation (HYPORT) after lumpectomy for patients with stage I-IIA breast cancer treated with breast conservation therapy.
• To determine the local tumor control and distant tumor control rates for patients with stage I-IIA breast cancer treated with breast conservation therapy using IOERT and HYPORT after lumpectomy.
• To determine the long-term side effects and cosmetic outcome of IOERT to tumor bed and HYPORT after lumpectomy for patients with stage I-IIA breast cancer.

OUTLINE: Patients undergo lumpectomy per standard procedures. Patients undergo intraoperative electron irradiation (IOERT) to the tumor bed right after completion of lumpectomy with axillary lymph node dissection or sentinel lymph node biopsy.

Beginning 2-6 weeks after lumpectomy with axillary lymph node dissection/sentinel lymph node sampling and IOERT, patients receive hypofractionated external-beam irradiation once daily for 16 days.

After completion of study treatment, patients are followed at 3 months, every 6 months for 5 years, and then annually thereafter for 8 years.

Enrollment: 50 patients

Sex: Female

Ages: 21+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed primary invasive breast carcinoma

  • Stage I-IIA disease (T1, N0, M0 or T2, N0, M0)

  • Pathologically determined single, discrete, and well-defined primary tumor ≤ 5 cm in diameter

    • Pathologically negative surgical margins

• No multicentric disease and/or diffuse malignant appearing microcalcifications

  • Micro-calcifications must be focal

    • Specimen radiograph is required after lumpectomy for tumors associated with malignant appearing calcifications to assure removal of all malignant appearing calcifications
    • Specimen radiograph is optional if the tumor appears as a discrete mass on mammogram

• No axillary lymph node involvement

• No evidence of metastatic breast cancer

• Hormone receptor status not specified

PATIENT CHARACTERISTICS:

• ECOG performance status 0-2
• Menopausal status not specified
• No pre-existing collagen vascular disease except rheumatoid arthritis that does not require immunosuppressive therapy
• Not pregnant or nursing

PRIOR CONCURRENT THERAPY:

• No prior irradiation to the area of planned radiation field
• No prior placement of breast prosthesis in the treated breast
• Concurrent hormonal therapy with external-beam irradiation allowed