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Adjuvant Radiation Therapy Compared With Observation After Surgery in Treating Women With Estrogen Receptor Positive or Progesterone Receptor Positive Ductal Carcinoma In Situ of the Breast Who Are Receiving Tamoxifen or Anastrozole

Randomised Trial Testing Observation (No Radiotherapy) Against Radiotherapy In Women With Low-Risk Completely Excised ER Positive Ductal Carcinoma In Situ (DCIS) Of The Breast On Adjuvant Endocrine Therapy

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00077168
Enrollment
2000
Registered
2004-02-11
Start date
2004-04-30
Completion date
Unknown
Last updated
2009-02-09

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

Conditions

Breast Cancer

Keywords

ductal breast carcinoma in situ, breast cancer in situ

Brief summary

RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells. It is not yet known whether radiation therapy after surgery is effective in preventing a recurrence of ductal carcinoma in situ. PURPOSE: This randomized phase II trial is studying adjuvant radiation therapy to see how well it works compared to observation after surgery in treating women with estrogen receptor positive or progesterone receptor positive ductal carcinoma in situ and are also receiving either tamoxifen or anastrozole.

Detailed description

OBJECTIVES: Primary * Compare ipsilateral tumor relapse and breast cancer metastases in women with completely excised low-risk estrogen receptor- or progesterone receptor-positive ductal carcinoma in situ of the breast receiving adjuvant tamoxifen or anastrozole and treated with adjuvant radiotherapy vs observation alone. * Compare the quality of life of patients treated with these regimens. Secondary * Determine the minimal surgical margins required to minimize the local recurrence rate in patients treated with these regimens. * Identify molecular markers that predict ipsilateral tumor recurrence in patients treated with these regimens. OUTLINE: This is a randomized, multicenter study. Patients are stratified according to participating center. Patients are randomized to 1 of 2 treatment arms. All patients receive adjuvant tamoxifen or anastrozole for 5 years. * Arm I: Patients undergo radiotherapy 5 days a week for 3 or 5 weeks. * Arm II: Patients undergo observation alone. Quality of life is assessed at baseline, at 6 months, and then at 1, 2, and 5 years. Patients are followed every 6 months for 1 year and then annually for up to 10 years. Peer Reviewed and Funded or Endorsed by Cancer Research UK PROJECTED ACCRUAL: A total of 2,000 patients (1,000 per treatment arm) will be accrued for this study within 5 years.

Interventions

DRUGanastrozole
DRUGtamoxifen citrate
PROCEDUREadjuvant therapy
RADIATIONradiation therapy

Sponsors

Institute of Cancer Research, United Kingdom
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Primary purpose
TREATMENT

Eligibility

Sex/Gender
FEMALE
Age
40 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Diagnosis of unifocal ductal carcinoma in situ of the breast without an invasive component * Microinvasion (defined as 1 or more foci of invasion each \< 1 mm) allowed * Prior complete microscopic excision (within the past 6 months) with a minimum radial margin of 1 mm by specimen x-ray required * Maximum microscopic tumor diameter \< 30 mm (\< 15 mm if grade 3 tumor) * Planning to receive adjuvant tamoxifen or anastrozole for 5 years * Eligible patients may receive adjuvant endocrine therapy on ICR-IBIS-II * Hormone receptor status: * Estrogen receptor positive OR * Progesterone receptor positive * More than 10% tumor staining for receptor OR a cutpoint of ≥ 2 PATIENT CHARACTERISTICS: Sex * Female Menopausal status * Premenopausal, perimenopausal, or postmenopausal Performance status * Not specified Life expectancy * Not specified Hematopoietic * Not specified Hepatic * Not specified Renal * Not specified Cardiovascular * No prior deep vein thrombosis Pulmonary * No prior pulmonary embolus Other * No unexplained postmenopausal bleeding * No contraindication to full-dose radiotherapy to the breast * No other cancer within the past 5 years except nonmelanoma skin cancer or carcinoma in situ of the cervix PRIOR CONCURRENT THERAPY: Biologic therapy * Not specified Chemotherapy * Not specified Endocrine therapy * See Disease Characteristics * No prior tamoxifen or raloxifene use for more than 3 months in duration Radiotherapy * Not specified Surgery * See Disease Characteristics * No prior mastectomy Other * No concurrent anticoagulants

Design outcomes

Primary

MeasureTime frame
Local tumor control (invasive and in situ local recurrence)

Secondary

MeasureTime frame
Pattern of relapse in the breast
Contralateral primary
Breast cancer metastases
Mastectomy rate
Quality of life
Molecular markers that predict ipsilateral tumor recurrence
Mortality

Countries

United Kingdom

Outcome results

None listed

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