Medical hyperspectral imaging to facilitate residual tumor identification during surgery

Introduction: Adequate evaluation of breast tumor resection at surgery continues to be an important issue in surgical care, as over 30% of postoperative tumors recur locally unless radiation is used to destroy remaining tumor cells in the field. Medical Hyperspectral Imaging (MHSI) delivers near-real time images of biomarkers in tissue, providing an assessment of pathophysiology and the potential to distinguish different tissues based on spectral characteristics. Method: We have used an experimental DMBA-induced rat breast tumor model to examine the intraoperative utility of MHSI, in distinguishing tumor from normal breast and other tissues. Rats bearing tumors underwent surgical exposure and MHSI imaging, followed by partial resection of the tumors, then MHSI imaging of the resection bed, and finally total resection of tumors and of grossly normal-appearing glands. Resected tissue underwent gross examination, MHSI imaging, and histopathological evaluation. Results: An algorithm based on spectral characteristics of tissue types was developed to distinguish between tumor and normal tissues. Tissues including tumor, blood vessels, muscle, and connective tissue were clearly identified and differentiated by MHSI. Fragments of residual tumor 0.5 - 1 mm in size intentionally left in the operative bed were readily identified. MHSI demonstrated a sensitivity of 89% and a specificity of 94% for detection of residual tumor, comparable to that of histopathological examination of the tumor bed (85% and 92%, respectively). Conclusion: We conclude that MHSI may be useful in identifying small residual tumor in a tumor resection bed and for indicating areas requiring more extensive resection and more effective biopsy locations to the surgeon. 3

[1]  W. Wetsel,et al.  Dietary fat and DMBA mammary carcinogenesis in rats. , 1981, Cancer detection and prevention.

[2]  N Kollias,et al.  Spectroscopic characteristics of human melanin in vivo. , 1985, The Journal of investigative dermatology.

[3]  T. Frazier,et al.  Implications of accurate pathologic margins in the treatment of primary breast cancer. , 1989, Archives of surgery.

[4]  D W Rattner,et al.  Impairment of pancreatic microcirculation correlates with the severity of acute experimental pancreatitis. , 1994, Journal of the American College of Surgeons.

[5]  N Kollias,et al.  Reduction of ischemia-reperfusion injury by monoclonal antibody to intercellular adhesion molecule-1. , 1996, Transplantation proceedings.

[6]  Michael G. Sowa,et al.  FTIR/NIR ASSESSMENT OF ISCHEMIC DAMAGE IN THE RAT HEART , 1997 .

[7]  A. E. Rogers Diet and breast cancer: studies in laboratory animals. , 1997, The Journal of nutrition.

[8]  N Kollias,et al.  Oxyhemoglobin is a quantifiable measure of experimentally induced chronic tretinoin inflammation and accommodation in photodamaged skin. , 1997, Skin pharmacology : the official journal of the Skin Pharmacology Society.

[9]  P. Colarusso,et al.  Infrared Spectroscopic Imaging: From Planetary to Cellular Systems , 1998 .

[10]  R. Doornbos,et al.  The determination of in vivo human tissue optical properties and absolute chromophore concentrations using spatially resolved steady-state diffuse reflectance spectroscopy. , 1999, Physics in medicine and biology.

[11]  M. Gladwin,et al.  Noninvasive Determination of Spatially Resolved and Time-Resolved Tissue Perfusion in Humans During Nitric Oxide Inhibition and Inhalation by Use of a Visible-Reflectance Hyperspectral Imaging Technique , 2001, Circulation.

[12]  G. Zonios,et al.  Skin melanin, hemoglobin, and light scattering properties can be quantitatively assessed in vivo using diffuse reflectance spectroscopy. , 2001, The Journal of investigative dermatology.

[13]  D. Ferris,et al.  Multimodal Hyperspectral Imaging for the Noninvasive Diagnosis of Cervical Neoplasia , 2001, Journal of lower genital tract disease.

[14]  B. Cady,et al.  A Comparison of Ink-Directed and Traditional Whole-Cavity Re-Excision for Breast Lumpectomy Specimens With Positive Margins , 2001, Annals of Surgical Oncology.

[15]  S. Singletary Surgical margins in patients with early-stage breast cancer treated with breast conservation therapy. , 2002, American journal of surgery.

[16]  Michael G Sowa,et al.  Spectroscopic assessment of cutaneous hemodynamics in the presence of high epidermal melanin concentration. , 2002, Clinica chimica acta; international journal of clinical chemistry.

[17]  A. Giuliano,et al.  The time has come to change the algorithm for the surgical management of early breast cancer. , 2002, Archives of surgery.

[18]  R. Gillies,et al.  Systemic effects of shock and resuscitation monitored by visible hyperspectral imaging. , 2003, Diabetes technology & therapeutics.

[19]  R. Simmons,et al.  Factors Associated With Residual Breast Cancer After Re-excision for Close or Positive Margins , 2004, Annals of Surgical Oncology.

[20]  Thomas E. Lyons,et al.  Early changes in the skin microcirculation and muscle metabolism of the diabetic foot , 2005, The Lancet.

[21]  M. Dewhirst,et al.  Hyperspectral imaging of hemoglobin saturation in tumor microvasculature and tumor hypoxia development. , 2005, Journal of biomedical optics.

[22]  J. Mansfield,et al.  Hyperspectral imaging: a new approach to the diagnosis of hemorrhagic shock. , 2006, The Journal of trauma.

[23]  Tuan Vo-Dinh,et al.  Development of an Advanced Hyperspectral Imaging (HSI) System with Applications for Cancer Detection , 2006, Annals of Biomedical Engineering.