Registry for patients with advanced or metastatic breast cancer
A Prospective Registry Study in Patients With Unresectable Locally Advanced or Metastatic Breast Cancer (MBC)
This study is creating a registry to collect health information from patients with advanced or metastatic breast cancer to better understand how the disease is managed and what outcomes patients experience.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1867 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Spanish Breast Cancer Research Group Academic / other |
| Locations | 40 sites (Elche, Alicante and 39 other locations) |
| Trial ID | NCT02819882 on ClinicalTrials.gov |
What this trial studies
This observational study aims to create a registry for patients diagnosed with unresectable locally advanced or metastatic breast cancer since January 2016. It involves multiple centers and does not specify any treatment regimen, allowing physicians to make independent clinical decisions. Patients can withdraw from the study at any time, and their health information will be recorded and monitored throughout the study duration. The goal is to gather comprehensive data on disease management and patient outcomes.
Who should consider this trial
Good fit: Ideal candidates include adults aged 18 and older diagnosed with unresectable locally advanced or metastatic breast cancer since January 2016.
Not a fit: Patients with early-stage breast cancer or those who have not been diagnosed with unresectable disease may not benefit from this study.
Why it matters
Potential benefit: If successful, this registry could enhance understanding of treatment patterns and outcomes in advanced breast cancer, potentially leading to improved patient care.
How similar studies have performed: Other observational studies in cancer registries have shown success in improving treatment understanding and patient outcomes, indicating this approach is supported by prior evidence.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Patients (males or females) diagnosed with unresectable locally advanced or MBC (either after a recurrence or as first diagnosis) from January 2016 onwards. 2. Patients who died are allowed to be included on the study. 3. Able and willing to provide written informed consent if they are alive. 4. Age ≥ 18 years. 5. Availability to medical records access and all data related to the disease management. Exclusion Criteria: None
Where this trial is running
Elche, Alicante and 39 other locations
- Hospital General de Elche — Elche, Alicante, Spain (Recruiting)
- Althaia-Xarxa Assistencial de Manresa — Manresa, Barcelona, Spain (Recruiting)
- Consorci Sanitari de Terrassa — Terrassa, Barcelona, Spain (Recruiting)
- Hospital Universitario Donostia — San Sebastián, Donostia, Spain (Recruiting)
- Hospital Dr. Negrín — Las Palmas de Gran Canaria, Gran Canaria, Spain (Recruiting)
- Hospital Universitario Fundación Alcorcón — Alcorcón, Madrid, Spain (Recruiting)
- Hospital Universitario de Fuenlabrada — Fuenlabrada, Madrid, Spain (Recruiting)
- Hospital Universitario Severo Ochoa — Leganés, Madrid, Spain (Recruiting)
- Hospital Infanta Sofía — San Sebastián de los Reyes, Madrid, Spain (Recruiting)
- Hospital Son Llatzer — Palma de Mallorca, Mallorca, Spain (Recruiting)
- Complejo Hospitalario de Navarra — Pamplona, Navarre, Spain (Recruiting)
- Hospital Universitario de Canarias — Santa Cruz de Tenerife, Tenerife, Spain (Recruiting)
- Hospital de Sagunto — Sagunto, Valencia, Spain (Recruiting)
- Hospital Universitario de Basurto — Bilbao, Vizcaya, Spain (Recruiting)
- Complejo Hospitalario Universitario A Coruña — A Coruña, Spain (Recruiting)
- Complejo Hospitalario Universitario de Albacete — Albacete, Spain (Recruiting)
- Hospital San Juan de Alicante — Alicante, Spain (Recruiting)
- Hospital Nuestra Señora de Sonsoles — Ávila, Spain (Recruiting)
- Hospital del Mar — Barcelona, Spain (Recruiting)
- Hospital Clinic de Barcelona — Barcelona, Spain (Withdrawn)
- Hospital Santa Creu i Sant Pau — Barcelona, Spain (Recruiting)
- ICO L´Hospitalet — Barcelona, Spain (Recruiting)
- Hospital Universitario Germans Trias i Pujol — Barcelona, Spain (Recruiting)
- Hospital Moisés Broggi_institut Catalá D´Oncologia — Barcelona, Spain (Recruiting)
- Hospital Universitario Reina Sofía — Córdoba, Spain (Recruiting)
- Hospital de León — León, Spain (Recruiting)
- Hospital Lucus Augusti — Lugo, Spain (Recruiting)
- Hospital Universitario La Princesa — Madrid, Spain (Recruiting)
- Hospital General Universitario Gregorio Marañón — Madrid, Spain (Recruiting)
- Hospital Universitario de Málaga — Málaga, Spain (Recruiting)
- Hospital Clínico Universitario Virgen de la Arrixaca — Murcia, Spain (Recruiting)
- Hospital Clínico Universitario de Salamanca — Salamanca, Spain (Recruiting)
- Hospital Universitario Virgen del Rocío — Seville, Spain (Recruiting)
- Hospital Virgen de la Salud — Toledo, Spain (Recruiting)
- IVO-Instituto Valenciano de Oncología — Valencia, Spain (Recruiting)
- Hospital Clínico Universitario de Valencia — Valencia, Spain (Recruiting)
- Hosital General de Valencia — Valencia, Spain (Recruiting)
- Hospital Universitario Dr. Peset — Valencia, Spain (Recruiting)
- Hospital Clínico Lozano Blesa — Zaragoza, Spain (Recruiting)
- Hospital Miguel Servet — Zaragoza, Spain (Recruiting)
Study contacts
- Study coordinator: MS Study Project Manager
- Email: inicio_ensayos@geicam.org
- Phone: +34 916892870
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.