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

SWOG Cancer Research Network

Status and phase: Terminated; Phase 3

Conditions: Breast Cancer

Treatments: Radiation: radiation therapy; Procedure: surgery

Study type: Interventional

Funder types: Other; NETWORK; NIH

Identifiers

NCT00005983

CAN-NCIC-MA25 (Other Identifier)

CLB-49910 (Other Identifier)

RTOG-9915 (Other Identifier)

S9927 (Other Identifier)

U10CA032102 (U.S. NIH Grant/Contract)

CDR0000067971

Details and patient eligibility

About

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.

Full 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.

Enrollment: 98 patients

Sex: Female

Ages: 21+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion 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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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98 participants in 2 patient groups

surgery

Active Comparator group

Description:

surgery followed by observation

Treatment:

Procedure: surgery

surgery followed by RT

Experimental group

Description:

Surgery followed by radiation therapy

Treatment:

Procedure: surgery

Radiation: radiation therapy