We expect that from a panel of possible protein-based biomarkers for the early detection of breast cancer, a small number of markers will be highly distinctive and able to detect breast cancer 1-2 years before diagnosis.
ID
Bron
Verkorte titel
Aandoening
Breast cancer, hereditary breast cancer
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Analyzing the differences in protein profiles between patients and controls and within patients over time. Moreover, establishing a panel of protein-based biomarkers for the early detection of breast cancer.
Achtergrond van het onderzoek
The purpose of a screening program is to identify breast cancer at an early stage before (regional) metastatic spread with the aim of improving the survival time of patients. However, currently, still a lot of cancer cases are missed. Especially in the high-risk group, mammography has a low performance and high numbers of interval cancers are being reported. The use of MRI next to mammography may improve the sensitivity in this group, but the specificity is variable, the technique is time-consuming and costs are high. Thus, there is a need to improve the screening for the early detection of breast cancer.
A specific and more sensitive addition to these imaging-based techniques could be the use of proteomic biomarkers. Therefore, in this study, the aim is to identify prediagnostic changes in protein biomarker levels between serial samples from the same study subject and between study subjects (cases and controls) and to identify a panel of protein-based biomarkers for the early detection of breast cancer in high-risk women. This will be studied by obtaining serum blood samples from high-risk women who visit the outpatient clinic for regular screening. On average, two samples will be collected every year, depending on the regular screening appointments. Protein profiles in serum will be analyzed using LC-MS.
Doel van het onderzoek
We expect that from a panel of possible protein-based biomarkers for the early detection of breast cancer, a small number of markers will be highly distinctive and able to detect breast cancer 1-2 years before diagnosis.
Onderzoeksopzet
Every 6 months (during regular screening appointments) until disease onset and at the moment of cancer discovery
Onderzoeksproduct en/of interventie
Blood draw once every 6 months
Algemeen / deelnemers
Wetenschappers
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- Women
- 25-75 years old
- Screening indication due to familiar or genetically enhanced risk of developing breast cancer or LTR > 15%
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Previous invasive breast cancer in medical history
- Other malignancies within the last 10 years (other than basal cell carcinoma)
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
Toelichting
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL8724 |
Ander register | METC Leiden Den Haag Delft (LDD) : METC 16.260 (CCMO: NL59318.058.16) |