Quantitative Subharmonic Breast Imaging

Thomas Jefferson University

Status and phase

Completed

Phase 4

Conditions

Breast Cancer

Treatments

Drug: 3D HI and SHI of UCA

Study type

Interventional

Funder types

Other

Industry

NIH

Identifiers

NCT01490892

JT 2179 (Other Identifier)

R01CA140338 (U.S. NIH Grant/Contract)

11F.438

Details and patient eligibility

About

This is a non-randomized trial of 450 women with a breast abnormality, who are scheduled for a breast biopsy of this abnormality. The study will be conducted at two clinical sites. The primary objective of this trial is:

To evaluate if quantitative 3D Subharmonic imaging (SHI) or pulse inversion harmonic imaging (HI) can improve the characterization of benign and malignant breast masses (independently or in combination with other imaging modes) compared to x-ray mammography, fundamental grayscale ultrasound (US) or power Doppler imaging (PDI).

The secondary aim of this trial is:

To compare quantitative (bifurcations & vessel length) and semi-quantitative (blood pool & parametric imaging) measures of the vascular morphology of breast lesions determined by pathology and by SHI.

Full description

This is an open-label, non-randomized trial that will be conducted at two clinical sites (the Breast Imaging Centers at Thomas Jefferson University (TJU) Hospital and University of California, San Diego (UCSD) Hospital). All 450 subjects will receive at most two IV bolus injections of Definity (Lantheus Medical Imaging, Billerica, MA), will undergo an unenhanced (baseline) and Definity contrast-enhanced US imaging study for evaluation of a breast mass or breast abnormality without mass, and will be scheduled to undergo a clinically indicated biopsy of the breast lesion under investigation.

Enrollment

219 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Be a female diagnosed by x-ray mammography (performed within 90 days prior to the study procedure) as having a solid breast mass or abnormal area without a mass.
Be scheduled for a biopsy (core / excisional / lumpectomy) of the mass or region of abnormality or for mastectomy within 30 days after this study procedure.
Be at least 18 years of age.
Be medically stable.
If a female of child-bearing potential, must have a negative pregnancy test.
Have signed Informed Consent to participate in the study.

Exclusion criteria

Males
Females who are pregnant or nursing.
Patients whose breast lesion is unequivocally a cyst by unenhanced US.
Patients currently on chemotherapy or with other primary cancers requiring systemic treatment.
Patients who are medically unstable, patients who are seriously or terminally ill, and patients whose clinical course is unpredictable. For example:
Patients on life support or in a critical care unit.
Patients with unstable occlusive disease (eg, crescendo angina)
Patients with clinically unstable cardiac arrhythmias, such as recurrent ventricular tachycardia.
Patients with uncontrolled congestive heart failure (NYHA Class IV)
Patients with recent cerebral hemorrhage.
Patients with clinically significant and unstable renal and/or liver disease (eg, transplant recipients in rejection)
Patients who have undergone surgery within 24 hours prior to the study sonographic examination.
Patients with known hypersensitivity to perflutren
Patients who have received any contrast medium (X-ray, MRI, CT, of US) in the 24 hours prior to the research US exam
Patients with cardiac shunts.
Patients with congenital heart defects.
Patients with severe emphysema, pulmonary vasculitis, or a history of pulmonary emboli.
Patients with confirmed or suspected liver lesions.
Patients with respiratory distress syndrome.
Patients who have had excisional biopsy/lumpectomy of the current area of interest within the past 6 weeks.