National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
NCT Number: NCT01468883
Patients with biopsy proven breast cancer, clinical stage I and II, will be randomized to receive treatment by one of two methods: (1) total mastectomy and axillary dissection; or (2) excisional biopsy, axillary dissection, and definitive irradiation.
Data from single institutions and from retrospective comparisons suggest that definitive irradiation with cosmetically acceptable breast preservation offers survival and local control results equivalent to extirpative surgery. This study will test this hypothesis in a prospective, randomized manner. After primary therapy, subjects will be followed for: (1) survival; (2) sites of recurrence; (3) anatomic function; (4) complications of therapy; and (5) cosmesis.
Looking for future studies?
Notify Me18 year and older
Female
Interventional
Phase 3
Bethesda, Maryland, 20892, United States
Patients with biopsy proven breast cancer, clinical stage I and II, will be randomized to receive treatment by one of two methods: (1) total mastectomy and axillary dissection; or (2) excisional biopsy, axillary dissection, and definitive irradiation.
Data from single institutions and from retrospective comparisons suggest that definitive irradiation with cosmetically acceptable breast preservation offers survival and local control results equivalent to extirpative surgery. This study will test this hypothesis in a prospective, randomized manner. After primary therapy, subjects will be followed for: (1) survival; (2) sites of recurrence; (3) anatomic function; (4) complications of therapy; and (5) cosmesis.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Female patients of any age with a dominant breast mass meeting the following requirements are eligible for this protocol:
On clinical evaluation the tumor must be confined to the breast and axillary lymph nodes (stage I and II).
Biopsy of the tumor must be classified as a primary breast neoplasm of epithelial origin.
Patients must be geographically accessible for follow-up and willing to return for the follow-up at the NCI.
Patient must be mentally competent to understand and give informed consent for the protocol.
Exclusion criteria
Patients will be excluded from this protocol for the following reasons:
Advanced local disease or distant metastases (stage III and IV);
Inflammatory cancer;
Chronic diseases such as heart, lung, liver, kidney, blood, or metabolic disorders which may render the patient a poor operative risk;
History of another cancer other than skin cancer (non-melanoma);
Concurrent pregnancy or lactation;
Non-palpable lesions manifested only by nipple discharge or skin rash (Paget's disease);
Previous therapy to the breast cancer other than excisional biopsy;
Multiple masses or multiple suspicious areas on mammogram unless all but one are proven histologically benign; and
Bilateral breast carcinoma, either invasive or in-situ.
Modified radical mastectomy
Excisional biopsy plus radiation
Time frame: survival rate completion of study
To compare the results of excisional biopsy followed by radiation therapy versus modified radiacal mastectomy
National Cancer Institute (NCI)
Nih
The Treatment of Stage I and II Carcinoma of the Breast With Mastectomy and Axillary Dissection vs. Excisional Biopsy Axillary Dissection, and Definitive Irradiation
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06068257
Breast Cancer, Breast Diseases
Orlando, Florida, United States
View Trial DetailsNCT05754658
Breast Cancer, Breast Diseases
Philadelphia, Pennsylvania, United States
View Trial DetailsNCT07040514
Breast Cancer, Breast Diseases
Lebanon, New Hampshire, United States
View Trial DetailsNCT06604858
Breast Cancer, Breast Diseases
A Coruña, Spain
View Trial Details