Parent opinions regarding the genetic testing of minors for BRCA1/2

Angela R. Bradbury, Linda Patrick-Miller, Brian Egleston, Colleen Burke Sands, Tianyu Li, Helen Schmidheiser, Maia Feigon, Comfort N. Ibe, Fay J. Hlubocky, Kisha Hope, Sarah Jackson, Melanie Corbman, Olufunmilayo I. Olopade, Mary Daly, Christopher K. Daugherty

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Purpose: Although not currently recommended, genetic testing of minors for adult hereditary cancer syndromes, along with risks and benefits, is still being debated. Thus, we evaluated parent opinions regarding BRCA1/2 testing of minors, in general, and hypothetically, for parents' own minor child. Methods: Semistructured interviews were conducted to assess parent opinions regarding BRCA1/2 testing in minors, along with parent rationale for and factors associated with these opinions. Results In total, 246 parents at two academic cancer risk assessment programs who underwent BRCA1/2 testing completed the interview (60% response rate). In response to a dichotomous question, 37% of parents supported testing minors. Responses to an open-ended query suggest that 47% support testing minors in some or all circumstances. Parent negative BRCA1/2 test result (P = .02), parent male sex (P = .03), and minority race (P = .01) were independently associated with support of testing minors. In response to a dichotomous question, 44% of parents reported hypothetical interest in testing their own minor offspring. Responses to an open-ended query suggest that 55% would consider, hypothetically, testing their child in some or all circumstances. Parent negative test result (P = .01), less than a college education (P < .01), and older mean offspring age (P = .05) were associated with interest in testing one's own child. Conclusion: Parents' opinions regarding BRCA1/2 testing of minors are divided. Given the lack of evidence supporting either the permission or restriction of BRCA1/2 testing in minors, further evaluation of the risks and benefits of providing genetic risk information and genetic testing to minors for adult-onset disease is needed to inform clinical practice and guidelines.

Original languageEnglish
Pages (from-to)3498-3505
Number of pages8
JournalJournal of Clinical Oncology
Volume28
Issue number21
DOIs
StatePublished - Jul 20 2010

Keywords

  • Adolescent
  • Adult
  • Aged
  • Child
  • Child, Preschool
  • Female
  • Genes, BRCA1
  • Genes, BRCA2
  • Genetic Testing
  • Humans
  • Male
  • Middle Aged
  • Minors
  • Mutation
  • Parents

Fingerprint

Dive into the research topics of 'Parent opinions regarding the genetic testing of minors for BRCA1/2'. Together they form a unique fingerprint.

Cite this