4.8 Article

Investigation of Optical Coherence Microelastography as a Method to Visualize Cancers in Human Breast Tissue

Journal

CANCER RESEARCH
Volume 75, Issue 16, Pages 3236-3245

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/0008-5472.CAN-14-3694

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Funding

  1. Australian Research Council
  2. National Health and Medical Research Council (Australia)
  3. National Breast Cancer Foundation (Australia)
  4. Raine Medical Research Foundation
  5. Cancer Council Western Australia
  6. Gledden Trust of The University of Western Australia
  7. University of Western Australia

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An accurate intraoperative identification of malignant tissue is a challenge in the surgical management of breast cancer. Imaging techniques that help address this challenge could contribute to more complete and accurate tumor excision, and thereby help reduce the current high reexcision rates without resorting to the removal of excess healthy tissue. Optical coherence microelastography (OCME) is a three-dimensional, high-resolution imaging technique that is sensitive to microscale variations of the mechanical properties of tissue. As the tumor modifies the mechanical properties of breast tissue, OCME has the potential to identify, on the microscale, involved regions of fresh, unstained tissue. OCME is based on the use of optical coherence tomography (OCT) to measure tissue deformation in response to applied mechanical compression. In this feasibility study on 58 ex vivo samples from patients undergoing mastectomy or wide local excision, we demonstrate the performance of OCME as a means to visualize tissue microarchitecture in benign and malignant human breast tissues. Through a comparison with corresponding histology and OCT images, OCME is shown to enable ready visualization of features such as ducts, lobules, microcysts, blood vessels, and arterioles and to identify invasive tumor through distinctive patterns in OCME images, often with enhanced contrast compared with OCT. These results lay the foundation for future intraoperative studies. (C) 2015 AACR.

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