Actively Recruiting
Monitoring Response to NAC and Prediction of pCR in Breast Cancer Patients Using Optical Imaging
Led by IRCCS San Raffaele · Updated on 2024-09-19
20
Participants Needed
1
Research Sites
291 weeks
Total Duration
On this page
Sponsors
I
IRCCS San Raffaele
Lead Sponsor
P
Politecnico di Milano
Collaborating Sponsor
AI-Summary
What this Trial Is About
Neoadjuvant chemotherapy (NAC) is the first line treatment for locally advanced breast cancer (BC). Besides making breast conserving surgery feasible, its main aim is to achieve a pathological complete response (pCR). Previous studies demonstrated that a pCR correlated with a higher disease-free survival. Tumor response may vary among different BC subtypes and only 30% of BC respond completely to NAC. Treating chemo-resistant disease with NAC may cause patient harm due to drug toxicity and surgery delay. It is therefore very important to promptly identify those women who will not benefit from NAC. Mammography and ultrasound proved ineffective in monitoring changes in lesion size due to therapy-induced fibrosis. MRI is the most accurate imaging technique for assessing early clinical response by measuring tumor size, however its accuracy is lower post NAC. This necessitates the need for a new technique able to non invasively assess the effectiveness of NAC. Optical techniques are sensitive to the biological changes that occur within the tumor after NAC administration. These changes occur prior to tumor size reduction. Optically estimated total hemoglobin concentration correlates with the histological analysis of vasculature as well as with tumor-associated angiogenesis which can affect tumor changes during NAC. Other promising biomarkers related to tissue composition (water, lipid, collagen content) and structure (scattering) may also be evaluated by optical techniques. The aim of the study is to monitor the effectiveness of NAC in BC patients with a near infrared spectroscopic imaging platform which allows to non-invasively detect changes in vascularization and size of BC and to characterize the presence of temporal changes in regional concentrations of relevant biomarkers (oxy- and deoxyhemoglobin, water, lipid and collagen concentration, scattering) within tissue during NAC. This optical imaging technique will provide a non-invasive, safe and relatively inexpensive tool to monitor patients' response to NAC and to predict their outcome.
CONDITIONS
Official Title
Monitoring Response to NAC and Prediction of pCR in Breast Cancer Patients Using Optical Imaging
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women above 18 years of age
- Women with a recent diagnosis of breast cancer candidate for neoadjuvant chemotherapy
- Women willing to give informed consent
You will not qualify if you...
- Subject is pregnant or breastfeeding
- Subject is unable or unwilling to give informed consent
- Previous surgery of the same breast
- Presence of distant metastasis
- Breast implants
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Trial Site Locations
Total: 1 location
1
Ospedale San Raffaele
Milan, Italy, 20132
Actively Recruiting
Research Team
P
PIETRO PANIZZA, PI
CONTACT
C
CAROLINA SANTANGELO
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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