Informational needs of individuals from families harboring BRCApathogenic variants: A systematic review and content analysis

Personalized information is paramount to patient-centered communication and decision-making regarding risk management in hereditary cancer syndromes. This systematic review identified information needs of individuals from families harboring BRCApathogenic variants and compared findings based on gender (women vs men) and clinical characteristics (patients with cancer vs previvors and BRCAheterozygotes vs untested relatives).