Breast Cancer Clinical Trial
Official title:
A Pilot Study of CyberKnife Radiosurgery Delivered to the Partial Breast for Women With Stage 0, 1, or IIA (<=3cm) Breast Cancer
This pilot study will evaluate the technical feasibility and acute toxicity of Partial
Breast Irradiation (PBI) with the CyberKnife in anticipation of a larger multi-institutional
Phase II study. It will evaluate quality of life (QOL) issues as they relate to treatment
related side effects, cosmetic result, and patient convenience.
Radiosurgery is defined as the stereotactic delivery of ionizing radiation in 5 stages or
less to a designated target with sub-millimeter accuracy. Radiosurgery in the context of
this protocol will be given to the region of the tumor bed within 7 weeks of lumpectomy and
sentinel/axillary node sampling over a period of five to ten days using the CyberKnife (CK).
Subjects will receive CK before chemotherapy, if applicable.
n/a
Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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