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Comparison of germline mutations in African American and Caucasian men with metastatic prostate cancer.
Ledet, Elisa M; Burgess, Earle F; Sokolova, Alexandra O; Jaeger, Ellen B; Hatton, Whitley; Moses, Marcus; Miller, Patrick; Cotogno, Patrick; Layton, Jodi; Barata, Pedro; Lewis, Brian E; Nakazawa, Mari; Zhu, Jason; Dellinger, Beth; Elrefai, Sara; Nafissi, Nellie N; Egan, Jan B; Shore, Neal; McKay, Rana R; Bryce, Alan H; Cheng, Heather H; Antonarakis, Emmanuel S; Sartor, Oliver.
Afiliação
  • Ledet EM; Department of Medicine, Tulane Cancer Center, Tulane University, New Orleans, Louisiana, USA.
  • Burgess EF; Genitourinary Oncology Section, Levine Cancer Institute/Atrium Health, Charlotte, North Carolina, USA.
  • Sokolova AO; Division of Oncology, Department of Medicine, University of Washington Medical Center/Fred Hutchinson Cancer Research Center/VA Puget Sound HCS, Seattle, Washington, USA.
  • Jaeger EB; Department of Medicine, Tulane Cancer Center, Tulane University, New Orleans, Louisiana, USA.
  • Hatton W; Department of Medicine, Tulane Cancer Center, Tulane University, New Orleans, Louisiana, USA.
  • Moses M; School of Medicine, Tulane University, New Orleans, Louisiana, USA.
  • Miller P; Department of Medicine, Tulane Cancer Center, Tulane University, New Orleans, Louisiana, USA.
  • Cotogno P; Department of Medicine, Tulane Cancer Center, Tulane University, New Orleans, Louisiana, USA.
  • Layton J; Department of Medicine, Tulane Cancer Center, Tulane University, New Orleans, Louisiana, USA.
  • Barata P; Deming Department of Medicine, Tulane University, New Orleans, Louisiana, USA.
  • Lewis BE; Department of Medicine, Tulane Cancer Center, Tulane University, New Orleans, Louisiana, USA.
  • Nakazawa M; The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University, Baltimore, Maryland, USA.
  • Zhu J; Genitourinary Oncology Section, Levine Cancer Institute/Atrium Health, Charlotte, North Carolina, USA.
  • Dellinger B; Genitourinary Oncology Section, Levine Cancer Institute/Atrium Health, Charlotte, North Carolina, USA.
  • Elrefai S; Genitourinary Oncology Section, Levine Cancer Institute/Atrium Health, Charlotte, North Carolina, USA.
  • Nafissi NN; Internal Medicine, Mayo Clinic, Phoenix, Arizona, USA.
  • Egan JB; Center for Individualized Medicine, Mayo Clinic, Scottsdale, Arizona, USA.
  • Shore N; Carolina Urologic Research Center, Atlantic Urology Clinics, Myrtle Beach, South Carolina, USA.
  • McKay RR; Moores Cancer Center, University of California San Diego, La Jolla, California, USA.
  • Bryce AH; Division of Hematology/Oncology, Mayo Clinic Cancer Center, Mayo Clinic, Phoenix, Arizona, USA.
  • Cheng HH; Division of Oncology, Department of Medicine, University of Washington Medical Center/Fred Hutchinson Cancer Research Center/VA Puget Sound HCS, Seattle, Washington, USA.
  • Antonarakis ES; The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University, Baltimore, Maryland, USA.
  • Sartor O; Department of Medicine, Tulane Cancer Center, Tulane University, New Orleans, Louisiana, USA.
Prostate ; 81(7): 433-439, 2021 05.
Article em En | MEDLINE | ID: mdl-33792945
ABSTRACT

BACKGROUND:

The goal of this study is to evaluate germline genetic variants in African American men with metastatic prostate cancer as compared to those in Caucasian men with metastatic prostate cancer in an effort to understand the role of genetic factors in these populations.

METHODS:

African American and Caucasian men with metastatic prostate cancer who had germline testing using multigene panels were used to generate comparisons. Germline genetic results, clinical parameters, and family histories between the two populations were analyzed.

RESULTS:

A total of 867 patients were included in this retrospective study, including 188 African American and 669 Caucasian patients. There was no significant difference in the likelihood of a pathogenic or likely-pathogenic variants (PV/LPVs) between African American and Caucasian patients (p = .09). African American patients were more likely to have a variant of unknown significance than Caucasians (odds ratio [OR] = 1.95; p < .0001). BRCA1 PV/LPVs were higher in African Americans (OR = 4.86; p = .04). African American patients were less likely to have a PV/LPV in non-BRCA DNA repair genes (OR = 0.30; p = .008). Family history of breast (OR = 2.09; p = .002) or ovarian cancer (OR = 2.33; p = .04) predicted PV/LPVs in Caucasians but not African-Americans. This underscores the limitations of family history in AA men and the importance of personal history to guide germline testing in AA men.

CONCLUSIONS:

In metastatic prostate cancer patients, PV/LPVs of tested genes did not vary by race, BRCA1 PV/LPVs were more common in the African American subset. However, PV/LPVs in non-BRCA DNA repair genes were less likely to be encountered in African Americans. Family history associated with genetic testing results in Caucasians only.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Negro ou Afro-Americano / Mutação em Linhagem Germinativa / Proteína BRCA2 / População Branca / Metástase Neoplásica Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans / Male / Middle aged Idioma: En Revista: Prostate Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Negro ou Afro-Americano / Mutação em Linhagem Germinativa / Proteína BRCA2 / População Branca / Metástase Neoplásica Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans / Male / Middle aged Idioma: En Revista: Prostate Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos