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Exploring Prostate Cancer Patients' Interest and Preferences for Receiving Genetic Risk Information About Cancer Aggressiveness.
Roy, Siddhartha; Gwede, Clement K; Malo, Teri L; Scherr, Courtney L; Radlein, Selina; Meade, Cathy D; Vadaparampil, Susan T; Park, Jong Y.
Afiliación
  • Roy S; Penn State College of Medicine, Hershey, PA, USA.
  • Gwede CK; Moffitt Cancer Center, Tampa, FL, USA.
  • Malo TL; University of North Carolina, Chapel Hill, NC, USA.
  • Scherr CL; Northwestern University, Evanston, IL, USA.
  • Radlein S; Flatiron Health, New York, NY, USA.
  • Meade CD; Moffitt Cancer Center, Tampa, FL, USA.
  • Vadaparampil ST; Moffitt Cancer Center, Tampa, FL, USA.
  • Park JY; Moffitt Cancer Center, Tampa, FL, USA.
Am J Mens Health ; 14(3): 1557988320919626, 2020.
Article en En | MEDLINE | ID: mdl-32436757
ABSTRACT
The number of cases of aggressive prostate cancer is increasing. Differentiating between aggressive and indolent cases has resulted in increased difficulty for the physician and patient to decide on the best treatment option. Due to this challenge, efforts are underway to profile genetic risk for prostate cancer aggressiveness, which may help physicians and patients at risk for developing aggressive prostate cancer to select an appropriate treatment option. This study explores patients' interest in receiving genetic results, preference for how genetic risk information should be communicated, and willingness to share results with adult male first-degree relatives (FDRs). A nine-item survey was adapted to assess their beliefs and attitudes about genetic testing for prostate cancer aggressiveness. In addition, participants (n = 50) responded to hypothetical scenarios and questions associated with perceived importance of risk disclosure, preferences for receiving genetic risk information, and sharing of results with FDRs. As the hypothetical risk estimate for aggressive prostate cancer increased, patients' willingness to receive genetic risk information increased. This study found that most patients preferred receiving genetic risk education in the form of a DVD (76%), one-page informational sheet (75%), or educational booklet (70%). Almost all patients (98%) reported that they would be willing to share their test results with FDRs. The results of this study highlight prostate cancer patients' desire to receive and share genetic risk information. Future research should focus on assessing the long-term benefits of receiving genetic information for prostate cancer patients and implications of sharing this information with FDRs.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Revelación / Prioridad del Paciente Límite: Adult / Aged / Aged80 / Humans / Male / Middle aged Idioma: En Revista: Am J Mens Health Asunto de la revista: SAUDE PUBLICA / SERVICOS DE SAUDE Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Revelación / Prioridad del Paciente Límite: Adult / Aged / Aged80 / Humans / Male / Middle aged Idioma: En Revista: Am J Mens Health Asunto de la revista: SAUDE PUBLICA / SERVICOS DE SAUDE Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos