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The purpose of this study is to collect clinical data from women undergoing intra-operative radiation therapy to describe the effects, both good and bad, of IORT at the time of breast conservation surgery (lumpectomy) for early-stage breast cancer.
Only patients who, for clinical care are having IORT using the Xoft Axxent eBx System, will be eligible for research participation. Vulnerable populations will not be enrolled in this registry study, and only those patients who can verbalize their consent and sign for will be enrolled.
