Feature

2009 ◽  
Vol 13 (03) ◽  
pp. 22-36

Do Asian Breast Cancer Patients Have Poorer Survival Than Their Western Counterparts? A Comparison Between Singapore and Stockholm. Large Family With Both Parents Affected by Distinct BRCA1 Mutations: Implications For Genetic Testing.

2020 ◽  
Vol 28 (1) ◽  
pp. 281-286 ◽  
Author(s):  
J. Jaime Alberty-Oller ◽  
Sarah Weltz ◽  
Antonio Santos ◽  
Kereeti Pisapati ◽  
Meng Ru ◽  
...  

2017 ◽  
Vol 214 (1) ◽  
pp. 105-110 ◽  
Author(s):  
Laura Hafertepen ◽  
Alyssa Pastorino ◽  
Nichole Morman ◽  
Jennifer Snow ◽  
Deepa Halaharvi ◽  
...  

2007 ◽  
Vol 5 (4) ◽  
pp. 93
Author(s):  
D. Gabrys ◽  
K. Behrendt ◽  
E. Grzybowska ◽  
R. Suwinski ◽  
A. Idasiak ◽  
...  

2015 ◽  
Vol 33 (15_suppl) ◽  
pp. 1541-1541 ◽  
Author(s):  
Reshma Jagsi ◽  
Allison W. Kurian ◽  
Kent A. Griffith ◽  
Ann S. Hamilton ◽  
Kevin C. Ward ◽  
...  

2019 ◽  
Vol 37 (15_suppl) ◽  
pp. 1579-1579
Author(s):  
Sonya Reid-Lawrence ◽  
Tuya Pal ◽  
Ingrid A. Mayer ◽  
Xiao-Ou Shu ◽  
Ann Tezak ◽  
...  

1579 Background: Per national practice guidelines, pre-test genetic counseling (GC) through a board-certified or credentialed genetics health professional (GHP) is recommended when testing for hereditary cancer. We sought to compare differences in rates of pre-test GC among young breast cancer (BC) patients tested with or without GHP involvement across three racial groups (Black, Hispanic and non-Hispanic white (NHW)). Methods: A population-based sample of Black, Hispanic and NHW women diagnosed with invasive BC ≤ age 50 from 2009 to 2012 were recruited through the Florida State Cancer Registry. Participants were asked to complete a baseline questionnaire and release medical records for verification of clinical information and genetic testing. We compared the rates of pre-test GC across racial groups in women tested with or without GHP involvement using Analysis of Variance. Multivariate logistic regression analysis was also conducted to adjust for potential confounders. Results: Of 1618 participants, 828 had genetic testing based on medical records and/or self-reported on their questionnaire. There were 170 (20.5%) with GHP involvement (either through consultation and/or test ordering) and the remaining 658 women (79.5%) had no documentation of GHP involvement. Among patients tested without GHP involvement, rates of pre-test GC were significantly lower among Black women (34.8%) compared to Hispanics (80%) and NHW (78.7%) (p < 0.001). In contrast, among those with GHP involvement, rates of pre-test GC were similar among Black (89.7%), Hispanic (81.1%) and NHW (84.6%) (p = 0.89). Conclusions: Our results suggest that among young breast cancer patients tested for hereditary cancer without GHP involvement, Blacks were significantly less likely to receive pre-test GC, compared to the other two groups. In contrast, rates of pre-test GC among those with GHP involvement were similar across all groups. These results suggest a disparity in receipt of pre-test GC (which is standard of care per national guidelines) among Blacks tested without GHP involvement. These findings are concerning given the need to offer guideline-adherent care to all patients receiving hereditary cancer testing.


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