Breast CancerNeoadjuvant TherapyPathological ResponseInvasive Breast CarcinomaMicroRNAs
Study summary
This prospective observational study aims to investigate subtype-specific circulating microRNAs (miRNAs) and their association with response to neoadjuvant chemotherapy (NAC) in patients with breast cancer. Serum samples will be collected before NAC and prior to surgery, and changes in miRNA expression levels will be evaluated. Pathological complete response (pCR) and Miller-Payne scoring will be used to assess treatment response after NAC. The study also explores whether changes in circulating miRNA profiles can predict treatment response across different breast cancer subtypes. The findings may help identify biomarkers that support treatment planning and personalized therapy strategies.
Eligibility
Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Histologically confirmed breast cancer
* Planned to receive neoadjuvant chemotherapy
* Biologically female
* Age ≥ 18 years
* Ability to provide informed consent
* Adequate organ function to receive standard NAC (based on routine clinical evaluation)
Exclusion Criteria:
* Presence of metastatic disease at diagnosis
* Prior systemic chemotherapy for breast cancer
* Pregnancy or breastfeeding
* Active infection or uncontrolled comorbid conditions interfering with study participation
* Any condition preventing collection of blood samples
Primary outcome measure(s)
Change in circulating microRNA expression levels before and after neoadjuvant chemotherapy — Baseline (before NAC) and pre-surgery (after completion of NAC) Quantitative assessment of selected serum microRNAs (miR-200a/b/c, miR-34a, miR-221/222, miR-155, miR-146a) using RT-PCR. Changes in expression levels will be compared between baseline and pre-surgery samples.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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