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A Pilot Study of CyberKnife Radiosurgery Delivered to the Partial Breast for Women With Stage 0, 1, or IIA (<=3cm) Breast Cancer


N/A
45 Years
N/A
Not Enrolling
Female
Breast Cancer

Thank you

Trial Information

A Pilot Study of CyberKnife Radiosurgery Delivered to the Partial Breast for Women With Stage 0, 1, or IIA (<=3cm) Breast Cancer


Inclusion Criteria:



- DCIS or infiltrating ductal carcinoma of the breast <= 3cm

- margins clear by at least 2 mm

- age >=45 years

Exclusion Criteria:

- invasive lobular carcinoma

- multicentric disease

- nodal metastases

- breast implants

- pregnancy

- connective tissue disease

Type of Study:

Interventional

Study Design:

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

1. To evaluate the feasibility of CyberKnife body radiosurgery as the sole radiation therapy for this patient population 2. To evaluate the complication rate of CyberKnife body radiosurgery as the sole radiation therapy for this patient population

Outcome Time Frame:

1 year

Principal Investigator

Jefferson EC Moulds, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Georgetown University

Authority:

United States: Institutional Review Board

Study ID:

GUMC 2007-153

NCT ID:

NCT00529334

Start Date:

September 2007

Completion Date:

September 2008

Related Keywords:

  • Breast Cancer
  • Breast Cancer
  • Partial breast irradiation
  • Radiosurgery
  • CyberKnife
  • Radiotherapy
  • PBI
  • Breast Neoplasms

Name

Location
Georgtown University Medical Center Washington, District of Columbia  20057