MR Guided Focused Ultrasound Surgery in the Treatment of Breast Fibroadenomas

InSightec

Status and phase

Terminated

Phase 3

Conditions

Breast Fibroadenoma

Treatments

Device: ExAblate 2000

Study type

Interventional

Funder types

Industry

Identifiers

NCT00147108

BF002

Details and patient eligibility

About

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.

Full 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.

Enrollment

102 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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