Recruiting

Fluorescence Imaging

Sponsor:

University Health Network, Toronto

Code:

NCT01837225

Conditions

Breast Cancer

Eligibility Criteria

Sex: Female

Age: 18+

Healthy Volunteers: Not accepted

Study Details

Brief summary:

Breast cancer is the most commonly occurring cancer in women. Currently, breast conservation surgery (BCS) is the treatment most often prescribed. BCS involves removing the tumor while conserving the greatest amount of healthy breast tissue. Under standard white light, tumor borders are difficult for the surgeons to visualize. Therefore, between 30-70% of patients require a second operation to remove remaining cancerous tissue that wasn't detected during the initial surgery. Thus, there is an urgent clinical need for a new imaging tool that improves tumor visualization during the first surgery.

PRODIGI, a new hand-held optical imaging device, uses a safe violet-blue light to detect fluorescence signals in the tissue. Different tissues are associated with specific fluorescent colors and therefore the device can be used to differentiate between tumor and healthy breast tissue. Based on previous clinical data, PRODIGI can distinguish some tumors from normal tissues, but is not specific enough to detect a difference across all breast tumor types.

The fluorescent contrast drug 5-aminolevulinic acid (5-ALA) accumulates in tumors naturally and previous research has shown that 5-ALA increases tumor-normal tissue fluorescence contrast. In this observational clinical study, PRODIGI and 5-ALA will be used to visualize tumor borders during BCS. 5-ALA induced fluorescent images from the surgical sample and the surgical bed obtained by PRODIGI will be compared retrospectively with the images taken under standard white light and/or autofluorescence. The technology's ability to accurately identify tumor borders better than conventional practice will be confirmed by tissue pathology.

Conditions

Breast Cancer

Study ID

NCT01837225

Start date

Sep, 2010

Status verified date

Feb, 2024

Completion date

Aug 31, 2025

Anticipated

Primary completion date

Aug 31, 2025

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: Female

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Female patients with breast cancer
2. 18 years or older
3. Have consented for their standard surgeries for primary invasive breast cancers, with or without auxiliary procedure.
4. Have existing biopsies banked at the hospital (for ALA patients)

Exclusion Criteria:

1. Pre-operative therapy (including chemotherapy, endocrine therapy and radiotherapy)
2. Inability to consent
3. Prior history of photosensitivity, liver disease, or recurrent disease
4. Pregnancy
5. Absence of in-house core biopsy in tissue bank

Study Design

Enrollment

90 participants

Anticipated

Interventions and Outcome Measures

Arms

Control

Patients in the control arm will not receive the fluorescent contrast agent (5-ALA); however, intraoperative fluorescence imaging will still be performed. Patients will receive conventional breast conservation surgery and care independent of the contrast agent dose they receive.

Low Dose Contrast Agent

Patients in the low dose arm will receive 15 mg/kg 5-ALA fluorescent contrast agent administered orally 3 hours prior to intraoperative fluorescence imaging. Patients will receive conventional breast conservation surgery and care independent of the contrast agent dose they receive.

High Dose Contrast Agent

Patients in the high dose arm will receive 30 mg/kg 5-ALA fluorescent contrast agent administered orally 3 hours prior to intraoperative fluorescence imaging. Patients will receive conventional breast conservation surgery and care independent of the contrast agent dose they receive.

Intermediate Dose Contrast Agent

Patients in the intermediate dose arm will receive 20 mg/kg 5-ALA fluorescent contrast agent administered orally 3 hours prior to intraoperative fluorescence imaging. Patients will receive conventional breast conservation surgery and care independent of the contrast agent dose they receive.

Primary outcome measure

  • The sensitivities and specificities for the two (oral) doses of 5-ALA (15 mg/kg and 30 mg/kg) and control (0 mg/kg ALA) in differentiating cancer/normal tissue. [ Time Frame: The fluorescence and white-light images will be evaluated and compared to histopathology within an average of 2 months after the surgery. The sensitivities and specificities will be calculated within 4 months of achieving a full dataset (45 patients). ]

Central Contacts and Locations

Central contacts

Locations

Princess Margaret Hospital

Recruiting

Toronto, Ontario, Canada, M5T 2M9

Principal Investigator:

Ralph S DaCosta, PhD

More Information

Sponsor

University Health Network, Toronto

Last update posted

Feb 13, 2024

Last verified

Feb, 2024

Keywords

  • Fluorescence Imaging
  • Breast Tumor Margins
  • Real-time Assessment

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University Health Network, Toronto on 2024-02-13.