Establishment of a Nationwide Registry to Evaluate and Improve Risk-Based Prevention for Hereditary Breast and Ovarian Cancer (HerediCaRe)
- Gender
- Women and men
- Age
- 18 years and older
- Trial type
- Observational
- Line of therapy
- all
- Phase
- —
What is this trial about?
Some forms of breast and ovarian cancer are hereditary. People with an increased genetic risk for these diseases can receive care at centers affiliated with the German Consortium for Familial Breast and Ovarian Cancer, as well as at participating cancer centers. The goal of the HerediCaRe study is to establish a central, nationwide registry that collects information on the presence of risk factors, the effectiveness of preventive and therapeutic measures, and patients’ quality of life. Adults who have a hereditary predisposition (hereditary risk) for breast and/or ovarian cancer are eligible to participate.
Detailed description
Breast and ovarian cancer are common cancers among women. Studies show that 5–10% of breast cancer cases and about 10–15% of ovarian cancer cases are hereditary. People with a genetic predisposition to breast or ovarian cancer can seek care at the German Consortium for Familial Breast and Ovarian Cancer as well as at other cancer centers, where they can undergo regular screening and/or treatment. Now, a centralized nationwide registry is to be established to investigate open questions regarding the development and progression of hereditary breast and ovarian cancers.
The goal of the HerediCaRe study is to use this registry to evaluate and improve preventive measures. The study is an observational study that collects and analyzes patient data. This includes genetic analyses from blood samples as well as information on the patients’ well-being and quality of life. Based on this data, the study aims to identify additional tumor subtypes and gain a better understanding of subgroup-specific characteristics and risks. In the long term, the hope is that this will lead to an improved understanding and optimized prevention and treatment of breast and ovarian cancer.
Eligible participants are individuals aged 18 and older who have a genetically determined increased risk of breast or ovarian cancer. A hereditary form of the disease must be documented in the family and must have implications for treatment. The study does not test new medications or forms of treatment.
Facts
- Which disease: Breast cancer and/or ovarian cancer
- Cancer characteristics: familial (hereditary) risk for breast or ovarian cancer
- What the study investigates: Creation of a registry of all affected individuals receiving preventive care at cancer centers
- Study objective: to gain a better understanding of the disease and to evaluate the effect of preventive measures in individuals with an increased genetic risk for breast or ovarian cancer
- Study duration: no fixed observation period
- Study characteristics: observational study; no testing of new medications
Trial sites
31 trial sites in Germany are listed. Find a site near you.
Charité – Universitätsmedizin Berlin
Berlin
Status unknownZentrum Familiärer Brust- und Eierstockkrebs, Universitätsklinikum Dresden
Dresden
Status unknownZentrum Familiärer Brust- und Eierstockkrebs, Universitätsklinikum Düsseldorf
Düsseldorf
Status unknownFamiliäres Brust- und Eierstockkrebszentrum, Uniklinikum Erlangen
Erlangen
Status unknownKonsortialzentrum Familiärer Brust- und Eierstockkrebs, Universitätsklinikum Frankfurt
Frankfurt
Status unknownUniversitätsklinikum Freiburg
Hugstetter Straße 49, 79106 Freiburg
Recruiting
This list is compiled to the best of our knowledge but without guarantee: it may be incomplete, and a site's recruitment status can change at any time.
- Dr. med. Sebastian SommerSpecialist in internal medicine with a focus on hematology and oncology
- PD Dr. med. Matthias FröhlichSpecialist in internal medicine, immunology and emergency medicine
This description was translated into plain language by our medical editorial team. Whether participation is an option for you is a decision you make together with your treating physician.


