Radiation Therapy in Treating Women Who Have Undergone Breast Conservation Surgery and Systemic Therapy for Early Breast Cancer

Institute of Cancer Research, United Kingdom

Status and phase: Unknown; Phase 3

Conditions: Breast Cancer

Treatments: Radiation: intensity-modulated radiation therapy

Study type: Interventional

Funder types: Other

Identifiers

NCT00818051

ICR-IMPORT-HIGH

CDR0000629770

ICR-CTSU/2007/10013

EU-20897

ISRCTN47437448

Details and patient eligibility

About

RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. Specialized radiation therapy, such as intensity-modulated radiation therapy, that delivers a high dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue. It is not yet known which radiation therapy schedule is more effective in treating breast cancer.

PURPOSE: This randomized phase III trial is studying three different radiation therapy schedules to compare how well they work in treating women who have undergone breast conservation surgery and systemic therapy for early breast cancer.

Full description

OBJECTIVES:

• To test dose-escalated intensity-modulated radiotherapy after breast conservation surgery in women with early breast cancer who are at higher than average risk for local recurrence.

OUTLINE: This is a multicenter study. Patients are stratified according to center. Patients are randomized to 1 of 3 treatment arms.

• Arm I (control): Patients undergo sequential boost dose intensity-modulated radiotherapy (IMRT) 5 days a week for 4.6 weeks (23 fractions; 56 Gy).
• Arm II: Patients undergo concurrent boost dose IMRT 5 days a week for 3 weeks (15 fractions; 48 Gy).
• Arm III: Patients undergo concurrent boost dose IMRT 5 days a week for 3 weeks (15 fractions; 53 Gy).

Quality-of-life questionnaires are administered at baseline, 6 months, and at 1, 3, and 5 years. Photograph assessments of the breasts are taken at baseline and at 3 and 5 years. Blood samples are collected at baseline and periodically thereafter. Tissue samples are also collected from primary tumor, including new primary tumor in either breast, and recurrent tumor.

After completion of study treatment, patients are followed annually for 10 years.

Enrollment: 840 estimated patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed invasive breast cancer

  • Resectable, unilateral disease
  • T1-3, N0-1, M0 disease

• Has undergone prior breast conservation surgery with complete microscopic resection AND received appropriate systemic therapy for early breast cancer

• Requires a tumor bed boost plus whole breast radiotherapy as indicated by ≥ 1 of the following:

  • Age 18-49 years
  • Tumor size > 2.0 cm after primary surgery (maximum microscopic diameter of invasive component)
  • Tumor of any size treated by primary medical therapy
  • Grade III disease
  • Minimum microscopic margin of noncancerous tissue < 5 mm (excluding deep margin if at deep fascia)
  • Lymphovascular invasion
  • Axillary node positive

• Hormone receptor status not specified

PATIENT CHARACTERISTICS:

• Menopausal status not specified
• No prior malignancy other than non-melanoma skin cancer or carcinoma in situ of the cervix

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics
• No prior mastectomy
• No concurrent chemotherapy except primary or sequential chemotherapy

Trial design

840 participants in 3 patient groups

Arm I (control)

Active Comparator group

Description:

Patients undergo sequential boost dose intensity-modulated radiotherapy (IMRT) 5 days a week for 4.6 weeks (23 fractions; 56 Gy).

Treatment:

Radiation: intensity-modulated radiation therapy

Arm II

Experimental group

Description:

Patients undergo concurrent boost dose IMRT 5 days a week for 3 weeks (15 fractions; 48 Gy).

Treatment:

Radiation: intensity-modulated radiation therapy

Arm III

Experimental group

Description:

Patients undergo concurrent boost dose IMRT 5 days a week for 3 weeks (15 fractions; 53 Gy).

Treatment:

Radiation: intensity-modulated radiation therapy