Goals

  • To improve the recognition of hereditary cancer. For this we need to extend our knowledge of the phenotype of cancer predisposition syndromes and novel genetic factors.  To achieve this, both phenotypic and genetic DNA information from blood and tumors is essential. 
  • To improve the diagnostics of hereditary cancer and meet patient needs. For this we need to evaluate and optimize strategies to give patients access to genetic testing and the optimal genetic diagnostic test strategies.  
  • To improve the treatment of hereditary cancer. For this we need to evaluate the effect of current treatment strategies that mostly follow the guidelines of a given tumor type. As for our rare patient groups, more tailored treatment strategies are necessary and warrant exploration. The increasing knowledge on the mechanisms underlying the most frequent cancer predisposition syndromes provides ample opportunities to achieve this goal.  
  • To improve cancer prevention in individuals with a genetic predisposition to develop cancer. For this we need to optimize access to current multidisciplinary surveillance programs, risk reducing interventions (e.g., surgery or medication), and novel preventive measures such as vaccination, and to evaluate the efficiency of these measures. 


Research Research programs Hereditary cancer:

Our mission

We aim to improve aspects of the entire care pathway, from recognition to diagnosis and treatment as well as the prevention of hereditary cancer.


Goals

See some of the most important goals for this research program.

read more

Research groups contributing to this research program


Spokesperson

dr. Richarda de Voer

contact form

Spokesperson

prof. dr. Marjolijn Ligtenberg

contact form

Spokesperson

dr. Chella van der Post

contact form