This is a retrospective-prospective study design. Patients who completed treatment approximately 3 years (range of 2-4 years) at time of IRB approval of this study will be identified and any existing data in the patient's record will be collected in addition to conducting office visits for long-term follow-up.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Absence of Local Recurrence at Treatment Site(s) Greater or Equal to 3 Years Follow-up
Timeframe: Range greater or equal to 3 years post last Xoft eBx or MMS treatment at the time of study start at1 long-term prospective visit by study completion.