Clinical trial Recruiting at 4 sites Observational Ages 18 and up Women only

Understanding breast cancer through protein and molecular analysis

Official title: Breast Cancer Proteomics and Molecular Heterogeneity

Run by Cancer Trials Ireland · NCT01840293 · Data updated 2026-11-12

This study is trying to learn more about the proteins and genes in breast cancer tumors to see how they change over time and how they might affect treatment for patients.

Quick facts

Study typeObservational
Ages18 Years and up
SexWomen only
Enrollment1780 (estimated)
SponsorCancer Trials Ireland
Research network
Locations6 sites (Cork and 5 other locations)
StatusRecruiting
StartedFebruary 2013
Main results expectedDecember 2029
Study endsJanuary 2038
Registry record updatedDecember 19, 2025
Trial IDNCT01840293 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults diagnosed with primary breast cancer or those with suspected or confirmed recurrent/metastatic breast cancer.

Probably not a fit

Patients with non-breast cancer conditions or those unable to provide informed consent may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to define the proteomic and molecular characteristics of primary and recurrent/metastatic breast tumors, focusing on the expression of specific proteins and genes such as S100, estrogen receptor, progesterone receptor, and HER2. Patients will undergo standard treatment while tissue and blood samples are collected at various time points, including pre- and post-operative stages. The study also seeks to expand knowledge on the molecular pathways involved in breast cancer progression and their response to treatments, as well as to identify potential serum markers related to cancer progression.

Why it matters

Potential benefit: If successful, this study could lead to improved understanding of breast cancer biology and better-targeted therapies for patients.

How similar studies have gone: Other studies focusing on proteomics and molecular characteristics in breast cancer have shown promise, indicating potential for success in this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Patients diagnosed with primary breast cancer attending hospital for the resection of their tumour tissue

   Or

   -Patients with suspected or confirmed recurrent or metastatic breast cancer (Patient has a history of a biopsy- or surgically- (i.e. pathologically) confirmed primary breast cancer) attending hospital for the resection/biopsy and/or treatment of tumour tissue

   Or

   -Patient with suspected (but not necessarily biopsy confirmed) newly diagnosed stage 4 breast cancer attending hospital for the resection/biopsy and/or treatment of their tumour tissue
2. Patients receiving neoadjuvant treatment are also eligible (if applicable)
3. Patients have to be ≥ 18 years of age
4. Patients must be able to give informed consent

Where it's running

  • Cork University Hospital
    Cork, Ireland
    Recruiting
  • Beaumont Hospital
    Dublin, Ireland
    Recruiting
  • St. Vincent's University Hospital
    Dublin, Ireland
    Recruiting
  • University Hospital Waterford
    Waterford, Ireland
    Recruiting
  • St James's Hospital
    Dublin, Ireland
    Completed
  • University Hospital Limerick
    Limerick, Ireland
    Active not recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.