MR Guided Focused Ultrasound Surgery in the Treatment of Breast Fibroadenomas

Breast Fibroadenoma Clinical Trial

Official title:

Phase 3 Study of MR Guided Focused Ultrasound Surgery in the Treatment of Breast Fibroadenomas

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00147108
• Other study ID #: BF002
• Status: Terminated
• Phase: Phase 3
• First received: September 2, 2005
• Last updated: September 13, 2012
• Start date: January 2003
• Est. completion date: October 2005

Study information

• Verified date: September 2012
• Source: InSightec
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The primary objective of this pivotal study is to evaluate the safety and efficacy of FUS treatment of breast fibroadenomas. Our hypothesis is that FUS lesion ablation of a fibroadenoma will have the following results: a. lead to a decrease in lesion cross-sectional area of > 50% on palpation, and >65% in lesion volume as measured by MRI (both calculations assume an elliptical shape of the lesion in all 3 dimensions). b. this decrease in size, along with the softening of the treated volume will result in satisfactory clinical results in greater than 50 % of the patients.

Description:

Many patients are now diagnosed with breast fibroadenomas. These are generally detected during breast self-exams, or annual physicals as a smooth, rubbery, oval/elliptical lump in the breast. These patients then go on to receive mammograms, sonograms and usually a core biopsy for the differential diagnosis of benign disease (fibroadenoma) vs breast cancer. Although fibroadenomas are benign, they can be of great concern to the patient because of their ability to mask the presence of other lumps in the breast, they can be painful, cause a physical deformity of the breast or have other symptoms. The current treatment is surgical excision. Surgical removal is invasive and may be cosmetically undesirable to some patients. It would be advantageous to develop a non-invasive ablative method for treatment of this disease. Measures of the clinical success of patients who elect surgical removal of fibroadenomas are generally subjective, and evaluated primarily by the patient (lack of palpable lesion, pain free, and an acceptable cosmetic result). A non-randomized study is proposed to allow for a more practical approach in subject recruitment. Analysis on safety and efficacy will be performed through the use of MRI evaluation and physical exams.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 102
• Est. completion date: October 2005
• Est. primary completion date: August 2005
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Gender: Females only

• Histologic confirmation of breast fibroadenoma by large core (needle gauge range 11-14 ) biopsy.

• Single tumor per breast quadrant

• Tumor clearly visible on non-contrast MRI

• Age > 18 years 3.2.6 Signed informed consent

• Tumor 5 mm or larger as measured on pre-treatment MR.

Exclusion Criteria:

• Gender: male

• Focal breast lesion on MRI over 3.5 cm as evaluated by MRI

• Distance from the edge of the breast fibroadenoma to the skin less than 0.5-cm or ribs less than 1 cm.

• Microcalcifications within the lesion

• Known intolerance to the MRI contrast agent (Gadolinium or Magnevist) 3.3.6 Patients on dialysis.

• Hemolytic anemia (hematocrit<30)

• Patients with unstable cardiac status including: Unstable angina pectoris on medication Patients with documented myocardial infarction within six months of protocol entry Congestive heart failure requiring medication (other than diuretic) Patients on anti-arrhythmic drugs Severe hypertension (diastolic BP > 100 on medication)

• Patients with cardiac pacemakers

• ASA Score>2

• Severe cerebrovascular disease (multiple CVA or CVA within 6 months) 3.3.12 Individuals who are not able or willing to tolerate the required prolonged stationary prone position during treatment (approximately 3 hrs.) 3.3.13 Patients with breast implants

• Large patients who cannot fit in the magnet (weight>250 pounds), and patients with standard contraindications for MR imaging such as non-MRI compatible implanted metallic devices

• Patients on anti-coagulation therapy, or those with an underlying bleeding disorder.

• Patient has a prior history of breast cancer

• Patient has a prior history of laser or radiation therapy to the target breast

• Patient has a prior history of chemo therapy

Study Design

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

Related Conditions & MeSH terms

• Breast Fibroadenoma
• Fibroadenoma

Intervention

Device:
• ExAblate 2000

Locations

Country	Name	City	State
Japan	Breastopia Namba Hospital	Miyazaki-ken
United States	University MRI	Boca Raton	Florida
United States	Brigham & Women's Hospital	Boston	Massachusetts
United States	Cornell Vascular	New York	New York
United States	Virtua	Voorhees	New Jersey

Sponsors (1)

Lead Sponsor	Collaborator
InSightec

Countries where clinical trial is conducted

United States,  Japan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	treatment/ablation of breast fibroadenoma

External Links

•   Sponsor web page