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Patient communication of cancer genetic test results in a diverse population.
Ricker, Charité N; Koff, Rachel B; Qu, Chenxu; Culver, Julie; Sturgeon, Duveen; Kingham, Kerry E; Lowstuter, Katrina; Chun, Nicolette M; Rowe-Teeter, Courtney; Lebensohn, Alexandra; Levonian, Peter; Partynski, Katlyn; Lara-Otero, Karlena; Hong, Christine; Petrovchich, Iva M; Mills, Meredith A; Hartman, Anne-Renee; Allen, Brian; Ladabaum, Uri; McDonnell, Kevin; Ford, James M; Gruber, Stephen B; Kurian, Allison W; Idos, Gregory E.
Afiliação
  • Ricker CN; USC Norris Comprehensive Cancer Center, Los Angeles, CA, USA.
  • Koff RB; Stanford University Cancer Institute, Stanford, CA, USA.
  • Qu C; USC Norris Comprehensive Cancer Center, Los Angeles, CA, USA.
  • Culver J; USC Norris Comprehensive Cancer Center, Los Angeles, CA, USA.
  • Sturgeon D; USC Norris Comprehensive Cancer Center, Los Angeles, CA, USA.
  • Kingham KE; Stanford University Cancer Institute, Stanford, CA, USA.
  • Lowstuter K; USC Norris Comprehensive Cancer Center, Los Angeles, CA, USA.
  • Chun NM; Stanford University Cancer Institute, Stanford, CA, USA.
  • Rowe-Teeter C; Stanford University Cancer Institute, Stanford, CA, USA.
  • Lebensohn A; Stanford University Cancer Institute, Stanford, CA, USA.
  • Levonian P; Stanford University Cancer Institute, Stanford, CA, USA.
  • Partynski K; USC Norris Comprehensive Cancer Center, Los Angeles, CA, USA.
  • Lara-Otero K; Stanford University Cancer Institute, Stanford, CA, USA.
  • Hong C; USC Norris Comprehensive Cancer Center, Los Angeles, CA, USA.
  • Petrovchich IM; Stanford University Cancer Institute, Stanford, CA, USA.
  • Mills MA; Stanford University Cancer Institute, Stanford, CA, USA.
  • Hartman AR; Myriad Genetics, Salt Lake City, UT, USA.
  • Allen B; Myriad Genetics, Salt Lake City, UT, USA.
  • Ladabaum U; Stanford University Cancer Institute, Stanford, CA, USA.
  • McDonnell K; USC Norris Comprehensive Cancer Center, Los Angeles, CA, USA.
  • Ford JM; Stanford University Cancer Institute, Stanford, CA, USA.
  • Gruber SB; USC Norris Comprehensive Cancer Center, Los Angeles, CA, USA.
  • Kurian AW; Stanford University Cancer Institute, Stanford, CA, USA.
  • Idos GE; USC Norris Comprehensive Cancer Center, Los Angeles, CA, USA.
Transl Behav Med ; 8(1): 85-94, 2018 01 29.
Article em En | MEDLINE | ID: mdl-29385580
Research on the communication of genetic test results has focused predominately on non-Hispanic White (NHW) mutation-positive families with high-risk hereditary cancer conditions. Little is known about this process for racially and ethnically diverse individuals or for those with mutations in moderate risk genes. The communication behaviors of study participants who carry a gene mutation were analyzed 3 months after disclosure of genetic test results. Participants were queried about communication of their results, as part of a prospective study of multi-gene panel genetic testing. The responses of particpants who tested positive were analyzed by race/ethnicity and by level of cancer risk (high vs. moderate). Of the 216 mutation-positive study participants, 136 (63%) responded. Self-reported race/ethnicity was 46% NHW, 41% Hispanic, 10% Asian, and 2% Black. The majority (99.0%, n = 135) had shared their results with someone and 96% had told a family member (n = 130). Hispanic respondents were less likely to have told a healthcare provider about their results than NHW (29% vs. 68%, p < .0001). Asian respondents were less likely than NHW to encourage family members to undergo testing (OR = 0.1, p = .03); but Asian family members were more likely to undergo testing (OR = 8.0, p = .03). There were no differences in communication between those with a mutation in a high- or moderate-risk gene. Three months post genetic testing, communication of results was very high; 30% reported a family member underwent genetic testing. Further studies are needed to better understand the communication process in individuals from diverse racial/ethnic backgrounds.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Comportamento Social / Testes Genéticos / Predisposição Genética para Doença / Comunicação em Saúde / Neoplasias Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Transl Behav Med Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Comportamento Social / Testes Genéticos / Predisposição Genética para Doença / Comunicação em Saúde / Neoplasias Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Transl Behav Med Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos