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NCT03758976Recruiting

Sweden Cancerome Analysis Network - Breast Recurrence (SCAN-B-rec)

SCAN-B-rec: Infrastructure, Technology Platform and Clinical Research Development to Profile and Monitor Metastatic Breast Cancer

Source: ClinicalTrials.gov · Last updated 16 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Prospective multicenter observational study to assess molecular drivers of metastatic breast cancer and disease evolution upon therapeutic pressure. The main aim is to develop and validate prognostic, predictive and pathogenic markers in clinically well-characterized population-based material of breast cancer tumors and the corresponding normal tissue.These data will be used to characterize recurrent breast cancer on a molecular level, study tumor evolution, develop biomarkers of response/resistance to targeted therapy in the metastatic setting, enroll patients on targeted treatment clinical studies and to elucidate mechanisms of resistance to therapy.

Status (registry)
Recruiting
Study type
Observational
Enrollment
2000 (estimated)
First submitted
28 Nov 2018
Start date
21 Jan 2019
Primary completion date
1 Dec 2030
Lead sponsor
Lund University Hospital
NCT number
NCT03758976

What you commit to

  • Study type: Observational
  • Planned participants: 2000
  • From 21 Jan 2019 to the primary completion date, 1 Dec 2030
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Untreated psychiatric disorders that will impair the patient's ability to comply with study treatment or protocol.

Who the study is looking for

  • Patients with pathologically confirmed advanced breast cancer (ABC), including locally advanced inoperable disease and stage IV disease.
  • Age \> 18 years.
  • Performance status according to Eastern Cooperative Oncology Group (ECOG) ≤ 2.
  • ABC must be radiologically or clinically assessable, by means of at least one of the following techniques: clinical examination, computerized tomography (CT-scan), magnetic resonance imaging (MRI), bone scintigraphy or positron emission tomography (PET).
  • Patients must have a radiological evaluation done maximum 6 weeks prior to inclusion.
  • Signed informed consent according to ICH/GCP, and national/local regulations.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Lund University Hospital
Coordinator of this site? Confirm its status
LundSwedenRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.