"I have always lived with the disease in the family": family adaptation to hereditary cancer-risk

BMC Prim Care. 2022 Apr 23;23(1):93. doi: 10.1186/s12875-022-01704-z.

Abstract

Background: Hereditary cancer syndromes have been conceptualized as a family level process. The present study explores the complexity and challenges of family adaptation to the hereditary cancer syndrome, in the context of genetic counseling and long-term cancer risk management and follow-up surveillance.

Methods: We performed semi-structured interviews with 13 participants with one of the following hereditary cancer syndromes: Lynch Syndrome, Hereditary Diffuse Gastric Cancer Syndrome, Hereditary Breast and Ovarian Cancer Syndrome, or Familial Adenomatous Polyposis. The interview was developed through a participatory approach with the involvement of healthcare professionals and individuals with first-hand experience of living with the hereditary cancer syndromes.

Results: The family is the main source of information and emotional support to deal with hereditary cancer syndromes. Multiple individual adaptation processes and communal coping networks interact, influencing the emotional and health-related behavior of family members. This is affected and affects the family's communication and its' members reactions to disclosure, with consequent changes in relationships.

Conclusions: The systemic interdependent dynamics of family adaptation calls for family-centered care of genetic cancer syndromes.

Keywords: Family adaptation; Hereditary cancer syndrome; Patient and public involvement; Qualitative study.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Colorectal Neoplasms, Hereditary Nonpolyposis* / genetics
  • Female
  • Genetic Counseling
  • Genetic Predisposition to Disease / genetics
  • Genetic Testing
  • Humans
  • Neoplastic Syndromes, Hereditary* / genetics