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Clinical Trials (PDQ®)

Radiation Therapy in Treating Women Who Have Undergone Surgery for Early-Stage Invasive Breast Cancer

Basic Trial Information
Trial Description
     Summary
     Further Trial Information
     Eligibility Criteria
Trial Contact Information

Basic Trial Information

PhaseTypeStatusAgeSponsorProtocol IDs
Phase IIITreatmentClosed16 and overNCI, OtherMA20
CAN-NCIC-MA20, NSABP-CAN-NCIC-MA20, NCCTG-CAN-NCIC-MA20, RTOG-CAN-NCIC-MA20, SWOG-CAN-NCIC-MA20, TROG-CAN-NCIC-MA20, CDR0000067938, NCIC-MA20, NCT00005957

Trial Description

Summary

RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells. Radiation to the tumor site and surrounding area may kill more tumor cells. It is not yet known if radiation therapy to the breast alone following surgery is more effective than radiation therapy to the breast plus surrounding tissue in treating invasive breast cancer.

PURPOSE: This randomized phase III trial is studying radiation therapy to the breast alone to see how well it works compared to radiation therapy to the breast plus surrounding tissue in treating women who have undergone surgery for early-stage invasive breast cancer.

Further Study Information

OBJECTIVES:

  • Compare the overall survival, disease-free survival, isolated local regional disease-free survival, and distant disease-free survival in women with previously resected, early stage, invasive breast cancer treated with breast radiotherapy with or without regional radiotherapy.
  • Compare the toxic effects of these regimens in these patients.
  • Compare the quality of life of patients (in certain participating centers) treated with these regimens.
  • Compare the cosmetic outcomes in patients (in certain participating centers) treated with these regimens.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to number of positive nodes (0 vs 1-3 vs more than 3), number of axillary nodes removed (<10, > or equal to 10); type of chemotherapy (anthracycline containing vs other vs none), hormonal therapy (yes vs no), number of axillary lymph nodes excised*, and participating center. Patients are randomized to one of two treatment arms.

NOTE: * Patients with a negative sentinel node dissection with or without an axillary dissection will be stratified according to the total number of nodes removed

  • Arm I: Patients undergo standard breast radiotherapy alone 5 days a week for 5 weeks in the absence of disease progression or unacceptable toxicity.
  • Arm II: Patients undergo breast and regional radiotherapy 5 days a week for 5 weeks in the absence of disease progression or unacceptable toxicity.

Radiotherapy in both arms begins as soon as possible after randomization. Radiotherapy must begin within 8 weeks after completion of adjuvant IV chemotherapy, unless radiotherapy is administered concurrently with chemotherapy (i.e., cyclophosphamide, methotrexate, and fluorouracil [CMF]), or within 16 weeks after the last breast surgery for patients treated with hormonal therapy alone.

Quality of life is assessed (in patients in certain participating centers) within 2 weeks prior to randomization, during the last week of radiotherapy, at 3 and 9 months after completion of radiotherapy, and then annually until first distant disease recurrence.

Cosmetic outcome is assessed (in patients in certain participating centers) within 2 weeks prior to randomization, and then at 3 and 5 years after completion of radiotherapy or until first distant disease recurrence.

Patients are followed at 3, 6, and 9 months, every 6 months for 2 years, and then annually thereafter.

PROJECTED ACCRUAL: Approximately 1,822 patients will be accrued for this study within approximately 4 years.

Eligibility Criteria

DISEASE CHARACTERISTICS:

  • Histologically proven invasive carcinoma of the breast
  • No evidence of T4, N2-3, or M1 disease prior to surgery
  • Node positive or high-risk node negative
  • Prior breast-conserving therapy (BCT) (e.g., lumpectomy, partial mastectomy, or segmental mastectomy) and axillary node dissection or sentinel node biopsy required and must be a candidate for breast radiotherapy after BCT
  • Normally patients should have microscopically clear resection margins and those with positive margins should undergo reexcision
  • Patients with microscopically focally positive margins (defined as no greater than 3 times high power fields) are candidates for breast radiotherapy plus a boost to the lumpectomy site
  • Patients with prior sentinel node dissection eligible if node negative, but still meet high-risk criteria
  • If node positive, then a level I and II axillary dissection must be performed
  • No evidence of residual disease in axilla after dissection
  • Must be treated with currently accepted adjuvant systemic chemotherapy and/or hormonal therapy
  • High risk of regional and systemic recurrence due to one of the following:
  • Pathologically positive axillary lymph nodes
  • Pathologically negative axillary lymph nodes with one of the following:
  • Primary tumor greater than 5 cm
  • Primary tumor greater than 2 cm and less than 10 axillary lymph nodes excised and one of the following:
  • Estrogen receptor negative
  • Skarf-Bloom-Richardson grade 3
  • Lymphovascular invasion
  • Hormone receptor status:
  • Estrogen and progesterone receptor status known

PATIENT CHARACTERISTICS:

Age:

  • 16 and over

Sex:

  • Female

Menopausal status:

  • Premenopausal or postmenopausal

Performance status:

  • ECOG 0-2

Life expectancy:

  • At least 5 years

Hematopoietic:

  • Not specified

Hepatic:

  • SGOT and/or SGPT no greater than 3 times upper limit of normal (ULN)*
  • Alkaline phosphatase no greater than 3 times ULN* NOTE: * Patients with laboratory values greater than 3 times ULN may still be eligible if no metastatic disease by imaging examinations

Renal:

  • No serious nonmalignant renal disease

Cardiovascular:

  • No serious nonmalignant cardiovascular disease

Pulmonary:

  • No serious nonmalignant pulmonary disease

Other:

  • Not pregnant or nursing
  • Fertile patients must use effective contraception
  • No other serious nonmalignant disease (e.g., systemic lupus erythematosus or scleroderma) that would preclude definitive surgery or radiotherapy
  • No other malignancy except:
  • Nonmelanomatous skin cancer
  • Carcinoma in situ of the cervix or endometrium
  • Contralateral noninvasive breast cancer (unless prior radiotherapy to the contralateral breast)
  • Invasive carcinoma of the cervix, endometrium, colon, thyroid, or melanoma that was curatively treated at least 5 years prior to study participation
  • No psychiatric or addictive disorder that would preclude informed consent or study compliance

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • Not specified

Chemotherapy:

  • See Disease Characteristics
  • Concurrent standard adjuvant chemotherapy allowed

Endocrine therapy:

  • See Disease Characteristics
  • Concurrent standard adjuvant hormonal therapy allowed

Radiotherapy:

  • See Disease Characteristics

Surgery:

  • See Disease Characteristics

Trial Contact Information

Trial Lead Organizations/Sponsors

NCIC-Clinical Trials Group

National Cancer Institute

NSABP Foundation Inc

Radiation Therapy Oncology Group

Southwest Oncology Group

Trans-Tasman Radiation Oncological Group Incorporated

North Central Cancer Treatment Group

Timothy Joseph WhelanStudy Chair

David S. PardaStudy Chair

Julia R. WhiteStudy Chair

Lori J. PierceStudy Chair

Boon ChuaStudy Chair

Laura A. VallowStudy Chair

Link to the current ClinicalTrials.gov record.
NLM Identifer NCT00005957
ClinicalTrials.gov processed this data on October 20, 2014

Note: Information about this trial is from the ClinicalTrials.gov database. The versions designated for health professionals and patients contain the same text. Minor changes may be made to the ClinicalTrials.gov record to standardize the names of study sponsors, sites, and contacts. Cancer.gov only lists sites that are recruiting patients for active trials, whereas ClinicalTrials.gov lists all sites for all trials. Questions and comments regarding the presented information should be directed to ClinicalTrials.gov.

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