NearWave Optical Molecular Monitoring

Description

The purpose of this study is to assess the feasibility of the NearWave optical molecular monitoring system for monitoring therapy progression and predicting pathologic complete response (pCR) of breast cancer patients undergoing neoadjuvant chemotherapy (NAC).

Conditions

Breast Cancer, HER2-positive Breast Cancer, TNBC - Triple-Negative Breast Cancer, HER2-negative Breast Cancer, Invasive Breast Carcinoma

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Study Overview

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Study Details

Study overview

The purpose of this study is to assess the feasibility of the NearWave optical molecular monitoring system for monitoring therapy progression and predicting pathologic complete response (pCR) of breast cancer patients undergoing neoadjuvant chemotherapy (NAC).

NearWave Optical Molecular Monitoring for Predicting Complete Pathological Response (pCR) to Neoadjuvant Chemotherapy (NAC) in Breast Cancer Patients

NearWave Optical Molecular Monitoring

Condition
Breast Cancer
Intervention / Treatment

-

Contacts and Locations

Indianapolis

Indiana University Simon Comprehensive Cancer Center, Indianapolis, Indiana, United States, 46202

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Women ≥ 18 years old at the time of informed consent
  • 2. Ability to provide written informed consent and HIPAA authorization
  • 3. Patients who:
  • 1. have been diagnosed with invasive breast cancer by tissue biopsy and have not yet started any therapy for the disease; a) Subtype HER2 positive (IHC 3+ or if IHC 2+, then positive by FISH), with any ER status, OR b) Subtype TNBC, defined by: HER2 negative and ER/PR negative or low (ER and PR ≤ 9%, weak staining)
  • 2. with ≥2 cm tumor size in the largest dimension as measured by ultrasound, MRI, or mammography. If multifocal disease, at least one tumor must measure ≥2 cm
  • 3. are planned to receive neoadjuvant chemotherapy followed by surgery
  • 4. Will be at least two weeks out from biopsy of the primary lesion at the time of baseline visit
  • 5. Have a palpable breast mass as determined by a treating physician
  • 1. Patients with significant bruising or hematoma from diagnostic breast biopsy, as determined by clinical judgement (mild ecchymosis okay)
  • 2. Inflammatory breast cancer
  • 3. Prior breast cancer requiring surgery or radiation in either breast
  • 4. Pregnant or nursing due to changes in breast architecture
  • 5. Patients with a BMI of ≥ 40, unless the lesion is near the surface (\<3 cm from the skin surface), based on diagnostic scan measurements
  • 6. Patients with any tattoos on their breasts

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

Indiana University,

Study Record Dates

2025-07