FBnTP Imaging of Breast Cancer

Johns Hopkins Medicine

Status and phase: Terminated; Phase 1

Conditions: Breast Cancer

Treatments: Drug: FBnTP

Study type: Interventional

Funder types: Other

Identifiers

NCT02204462

NA_00084913 (Other Identifier)

J13162

Details and patient eligibility

About

Our preclinical studies suggest the capacity of the positron emission tomography imaging agent 18F-fluorobenzyl triphenyl phosphonium (FBnTP) to detects early-stage small breast tumors (e.g., DCIS), and differentiates benign from malignant masses with better accuracy than that obtained by existing breast imaging tools.

Full description

Breast cancer is the most widespread type of cancer among women in the USA, and the second leading cause of death. The National Cancer Institute estimates that in 2013, in the USA, 226,870 women will be diagnosed with breast cancer and 39,510 women will die of breast cancer, most of them of progressive metastatic disease. Early detection and treatment of the disease, when the tumor is still localized and at a high curability state, is the outmost important determinant of disease-free survival of breast cancer patients. Survival rate of women first diagnosed with pure early-stage noninvasive tumor (ductal carcinoma in situ- DCIS) is nearly 98%, which drops to 48% in patients with advanced disease.Yet, early detection of breast cancer is relatively poor. This is best exemplify by the astonishing percentage of benign biopsies; 80% of 1.7 million biopsies in the USA, at a cost of $3 billion; whereas, only small fraction (~20%) of newly diagnosed women are found to have pure DCIS.

Our preclinical studies suggest the capacity of the positron emission tomography (PET) imaging agent 18F-fluorobenzyl triphenyl phosphonium (FBnTP) to detects early-stage small breast tumors (e.g., DCIS), and differentiates benign from malignant masses with better accuracy than that obtained by existing breast imaging tools. Accordingly, the present protocol is designed to extend the preclinical findings into clinical studies in breast cancer women, and to assess the effectiveness of 18F-FBnTP in detecting breast malignant lesions, in comparison with magnetic resonance imaging and fluorodeoxyglucose PET imaging.

Enrollment: 4 patients

Sex: Female

Ages: 26+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Female patients with newly-diagnosed invasive and/or intraductal breast cancer detected by core needle or vacuum-assisted biopsy (i.e., index cancer)
• Age > 25 Ability and willingness to sign informed consent prior to any study procedure.
• Positive indication of disease on mammogram or MRI scan.
• Candidate for breast cancer surgery on the basis of recommendation of a breast cancer surgeon.
• Ability to undergo up to 90 minutes of PEM imaging.

Exclusion criteria

• Any active or chronic illness that, in the opinion of the investigators, would make the study unsafe or limit compliance with study procedures.
• Past or present history of active substance abuse (drug or alcohol).
• Inability to tolerate venous access.
• Pregnant females are excluded from this study. All females of child-bearing potential will undergo a serum pregnancy test within 48 hours prior to FBnTP administration.

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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4 participants in 1 patient group

Newly diagnosed breast cancer

Experimental group

Description:

Patients with newly-diagnosed invasive and/or intraductal breast cancer detected by core needle or vacuum-assisted biopsy (i.e. index cancer). Patients will undergo FBnTP PET imaging for detection of malignant breast cancer.

Treatment:

Drug: FBnTP