Social and ethical implications of BRCA testing.
1Department of Medicine, Division of Medical Oncology, New York University Medical School, 550 First Avenue, BCD 556, New York, NY, USA. antonella.surbone@nyumc.org
Summary
Genetic testing for cancer susceptibility, like BRCA testing, raises complex ethical issues. Understanding genetic responsibility and preventing genetic discrimination are crucial for patient care and societal acceptance.
Area of Science:
- Medical Ethics
- Genetic Counseling
- Social Science
Background:
- Oncologists increasingly counsel patients on genetic testing for cancer susceptibility.
- Genetic testing includes physician-prescribed and direct-to-consumer options.
- Ethical and social implications require careful consideration.
Purpose of the Study:
- To critically review the ethical and social implications of BRCA testing.
- To focus on the concepts of genetic responsibility and genetic discrimination.
- To explore the balance between individual rights, community rights, and patient autonomy.
Main Methods:
- Literature review and critical analysis of ethical and social issues.
- Examination of the concept of genetic responsibility in the context of cancer predisposition.
- Analysis of genetic discrimination faced by mutation carriers and at-risk individuals.
Main Results:
- Genetic testing for cancer predisposition involves complex ethical considerations regarding individual and community rights.
- Physicians face ethical dilemmas balancing patient confidentiality with a duty to warn at-risk relatives.
- Genetic discrimination remains a concern, leading some individuals to forgo testing, despite legal protections.
Conclusions:
- Genetic responsibility necessitates a reevaluation of autonomy as relational.
- Legislation offers protection against genetic discrimination but is insufficient.
- Profound cultural shifts are needed for full understanding and acceptance of genetic differences.
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