Clinical trial Recruiting at 1 site Observational Ages 18 and up

Breast cancer subtypes and outcomes in Colombian women

Official title: Evaluation of Clinical and Therapeutic Outcomes According to Molecular Subtype in Patients With Breast Cancer: Experience of Fundación Santa Fe de Bogotá

Run by Fundación Santa Fe de Bogota · NCT07856225 · Data updated 2026-11-12

This study looks back at medical records of women with breast cancer to see how different molecular subtypes relate to survival and recurrence in a single Colombian hospital.

More Breast Neoplasms trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment370 (estimated)
SponsorFundación Santa Fe de Bogota
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Bogotá, Bogota D.C.)
StatusRecruiting
StartedDecember 1, 2025
Main results expectedJune 1, 2027
Study endsJune 1, 2027
Registry record updatedOctober 2, 2026
Trial IDNCT07856225 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Women 18 years or older with histologically confirmed breast cancer and documented molecular subtype treated at the center between 2014 and 2024.

Probably not a fit

Patients whose records lack complete molecular subtype or outcome data may not contribute to certain analyses.

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

What this trial studies

This is a retrospective cohort analysis of women aged 18 and over with biopsy-confirmed breast cancer and documented molecular subtypes treated at Fundación Santa Fe de Bogotá from 2014 to 2024. It describes the distribution of subtypes (including luminal A, luminal B with/without HER2, HER2-enriched, triple-negative, and HER2-low) and examines associations between clinical, molecular, and treatment factors with overall survival and progression-free survival, with an economic component using micro-costing from the health system perspective. The study uses an umbrella design to enable subtype- and treatment-specific secondary analyses and integrates an assessment of cost of illness by stage and care phase. Interventions observed include standard treatments, CDK4/6 inhibitors, and anti-HER2 therapies as part of routine care. The project aims to inform local practice by linking subtype characteristics to outcomes and costs in Colombia.

Why it matters

Potential benefit: If successful, the study could clarify how molecular subtypes relate to outcomes and costs, informing more tailored care and resource planning.

How similar studies have gone: Previous regional studies describe subtype distributions, but this is one of the first to combine clinical, molecular, treatment, and cost data in a single Colombian cohort.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients older than 18 years with a histopathologically confirmed diagnosis of breast cancer.
* Treated at Fundación Santa Fe de Bogotá between January 1, 2014 and December 31, 2024.
* Available record of the tumor molecular subtype (luminal A, luminal B HER2-negative, luminal B HER2-positive, HER2-enriched or triple-negative), determined by immunohistochemistry and/or in situ hybridization.

Exclusion Criteria:

* Metastatic tumors from another primary site involving the breast (for example, breast metastases from another primary tumor).
* Lesions of uncertain malignant potential or in situ tumors.
* Incomplete or missing information on molecular subtype, treatment received or clinical outcomes.
* Oncology follow-up outside the institution without adequate traceability of clinical outcomes.

Where it's running

  • Hospital Universitario Fundación Santa Fe de Bogotá
    Bogotá, Bogota D.C., Colombia
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.