HerediCaReRecruiting

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

  1. Which disease: Breast cancer and/or ovarian cancer
  2. Cancer characteristics: familial (hereditary) risk for breast or ovarian cancer
  3. What the study investigates: Creation of a registry of all affected individuals receiving preventive care at cancer centers
  4. 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
  5. Study duration: no fixed observation period
  6. 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 unknown
  • Zentrum Familiärer Brust- und Eierstockkrebs, Universitätsklinikum Dresden

    Dresden

    Status unknown
  • Zentrum Familiärer Brust- und Eierstockkrebs, Universitätsklinikum Düsseldorf

    Düsseldorf

    Status unknown
  • Familiäres Brust- und Eierstockkrebszentrum, Uniklinikum Erlangen

    Erlangen

    Status unknown
  • Konsortialzentrum Familiärer Brust- und Eierstockkrebs, Universitätsklinikum Frankfurt

    Frankfurt

    Status unknown
  • Universitätsklinikum 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.

Medical editorial team

  • 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.