Tissue- and Serum-Derived Exosomal microRNAs as Predictors of Neoadjuvant Chemotherapy Response in Breast Cancer
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Conditions studied: Breast Cancer, Invasive Breast Carcinoma, Exosomal microRNA, Neoadjuvant Chemotherapy Response, Pathological Complete Response
In brief
This prospective observational study aims to evaluate whether exosomal microRNA profiles derived from tumor tissue and blood serum are associated with pathological complete response (pCR) to neoadjuvant chemotherapy (NAC) in patients with breast cancer. Breast cancer patients with similar clinical and pathological features may respond differently to treatment, underscoring the need for reliable biomarkers that can help predict therapeutic outcomes. Exosomes are small extracellular vesicles released by tumor cells that carry molecular signals, including microRNAs, which may reflect tumor behavior and treatment sensitivity. In this study, patients with breast cancer receiving standard NAC as part of routine clinical care will be followed prospectively. Exosomal microRNA profiles obtained from tumor tissue and blood samples collected during routine diagnostic and treatment procedures will be analyzed and compared with pathological complete response (pCR) assessed after completion of neoadjuvant chemotherapy. A group of patients with benign breast disease will be included as a reference control for comparative analyses. The results of this study may contribute to the identification of minimally invasive biomarkers that support personalized treatment strategies in breast cancer.
Key facts
- Study ID
- NCT07500129
- Run by
- Atlas University
- People needed
- 60
- Starts
- 2026-04-12
- Expected to finish
- 2027-04-22
- Last updated by the study team
- 2026-03-30
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Female patients aged 18 years or older
- Histologically confirmed locally advanced breast cancer scheduled to receive neoadjuvant chemotherapy
- Availability of residual tumor tissue and/or serum samples obtained during routine clinical care
- Ability to provide written informed consent
You may not qualify if…
- Male sex
- Age under 18 years
- Prior systemic chemotherapy or radiotherapy administered for the current breast disease before enrollment.
- Evidence of metastatic disease at diagnosis (for breast cancer cohort)
- Pregnancy or breastfeeding
- Any condition that precludes the availability or adequate quality of tissue or blood samples for research purposes
Full record on ClinicalTrials.gov
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