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Monitoring the Response of Chemotherapy on Breast Cancer Tumor by Photon Migration Spectroscopy (PMS)

This study is enrolling participants by invitation only.
Information provided by University of California, Irvine

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Descriptive Information Fields
Brief Title  Monitoring the Response of Chemotherapy on Breast Cancer Tumor by Photon Migration Spectroscopy
Official Title  Monitoring the Response of Chemotherapy on Breast Cancer Tumor by Photon Migration Spectroscopy
Brief Summary

At Beckman Laser Institute, University of California, Irvine, we have continue developed diagnostic device call 'Photon Migration Spectroscopy'.

Optimal management of patients with locally advanced breast cancer (LABC) remains a complex therapeutic problem . LABC represents 5-20 % of all newly diagnosed breast cancers in the United States with a higher incidence in medically underserved areas. Over the years, treatment for LABC has been evolving from undergoing a radical mastectomy to the use of neoadjuvant chemotherapy followed by a mastectomy or breast conservation therapy. The optimal intensity and duration of neoadjuvant chemotherapy for LABC still remains controversial due to the difficulty of evaluating response to therapy . Consequently, it is very important to determine the optimal timing of the local surgical treatment of LABC patients. The goal would be to prevent over and under treatment of patients with neoadjuvant chemotherapy.

PMS is a non-invasive optical technique that utilizes intensity-modulated, near-infrared (NIR) light to quantitatively measure optical properties in thick tissues has been in use for clinical studies UCI HS#1995-563. Optical properties (absorption, µa, and scattering, µs', parameters) derived from PMS measurements can be used to construct low-resolution (0.5 -1 cm) functional images of tissue hemoglobin (total, oxy, and deoxy forms), oxygen saturation, blood volume fraction, water content, fat content and cellular structure. Unlike conventional NIR transillumination, PMS enables quantitative analysis of tissue absorption and scattering parameters in a single non-invasive measurement.

The unique functional information provided by PMS makes it well suited to characterizing tumors in thick tissues. Measurements are performed using a non-invasive, multi-wavelength, diode-laser PMS device. Some preliminary results show that the metabolic changes are detectable in locally advanced breast cancer tumors undergoing treatment with neoadjuvant chemotherapy using photon migration techniques. The measurements provide quantitative optical property values that reflect changes in tissue perfusion, oxygen consumption, and cell/matrix development.

Detailed Description

Non-invasive measurements of breast tissue optical properties will be performed on the skin surface using a specially designed PMS measurement probe which is similar in shape to an ultrasound probe. The PMS probe is embedded with optic fibers set at a fixed separation. The FDPM probe will be placed on different areas of the breast including areas suspected to have disease and areas appearing to be normal. The diseased location will be identified by clinical palpation. Some mild tissue compression will be performed within comfort tolerance of the patient during the application of the PMS probe.

When the probe is in position, the laser will be activated and a measurement will be taken. Each measurement will require about 30-60 seconds to record the data and calculate optical properties. The probe will then be turned off and moved to a new position for further measurements. The process will be repeated until an adequate number of measurements are performed (about 10-20). The whole process should take about 30 to 90 minutes.

Anticipate Risk and Benefit;

The optical scan is not expected to cause any pain, burning, or discomfort during or after the exam. There may be risks, however, that are currently unforeseeable. During all measurements, the laser will be turned on only when needed. Although not required for safety, subjects may wear protective eye goggles if requested.

There is no therapeutic benefit to the subject, especially none that might influence the indication for the diagnostic procedure as indicated. However, information obtained may lead to a new form of non-invasive imaging for the early detection of breast cancer.

Study Phase
Study Type  Observational
Study Design  Case-Only, Prospective
Primary Outcome Measure 
Secondary Outcome Measure 
Condition  Breast Cancer
Intervention  Device: DOS
MEDLINE PMIDs
Links
Recruitment Information Fields
Recruitment Status  Enrolling by invitation
Enrollment  57
Start Date  June 2002
Completion Date July 2012
Eligibility Criteria 

Inclusion Criteria:

  • Female non-pregnant and age greater than 21 years old but less than 75 years old
  • Diagnosed of Breast cancer and will be receiving neoadjuvant chemotherapy

Exclusion Criteria:

  • Female pregnant and age less than 21 years old and have no diagnosis of breast cancer
Gender Female
Ages 21 Years to 75 Years
Accepts Healthy Volunteers No
Contacts ††
Location Countries  United States
Administrative Information Fields
NCT ID  NCT00540852
Organization ID RR-01192, CA-10548
Secondary IDs †† DAMD17-02-1-0324, P41-RR01192;NIH-LAMMP, CA105480;NTROI
Study Sponsor  University of California, Irvine
Collaborators †† Beckman Laser Institute Medical Clinic
Chao Family Comprehensive Cancer Center
Genneral Clinical Research Center, University of California, Irvine
Investigators 
Principal Investigator:     David JB Hsiang, M.D     Beckman Laser Institute Medical Clinic    
Information Provided By University of California, Irvine
Verification Date January 2008
First Received Date  October 4, 2007
Last Updated Date January 3, 2008

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.




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