O05: Implementation of pan-cancer universal germline testing as standard of care in an ethnically diverse, rural, underserved community oncology practice

Universal germline genetic testing (GGT) is increasingly utilized in precision cancer care, including access to approved therapeutics, clinical trial enrollment, early detection or prevention of future cancers, and testing of at-risk family members. There is limited data on this approach in patients from historically underrepresented and underserved populations receiving care at community practices. However, these patients may benefit the most from universal GGT as studies show current GGT guidelines miss ∼50% of patients with pathogenic germline variants (PGVs), particularly among Black/African-American patients.

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Publication Details

Journal
Genetics in Medicine Open
Published
2025-01-01
DOI
https://doi.org/10.1016/j.gimo.2025.102030
Primary Topic
BRCA gene mutations in cancer
Type
article
Field-Weighted Citation Impact
0.00
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article

O05: Implementation of pan-cancer universal germline testing as standard of care in an ethnically diverse, rural, underserved community oncology practice

Rohan Nadkarni, Edward D. Esplin, Asutosh Gor, Alimitha Kodali et al.
Genetics in Medicine Open
BRCA gene mutations in cancer
article

O05: Implementation of pan-cancer universal germline testing as standard of care in an ethnically diverse, rural, underserved community oncology practice

Rohan Nadkarni, Edward D. Esplin, Asutosh Gor, Alimitha Kodali, Jai V. Patel, Niyati Nathwani, Sarah M. Nielsen, Viral Rabara, Carson Lee Gallo, Joseph M. DeSimone, Sashi Naidu, Brianna Bucknor, Priya Mathur, Kathryn E. Hatchell, Kirstie Parnell, Marian Łysiak, Adara Hubbert, Carlos Ortíz, Laura McDonald, Kashyap Patel, S Kaw, Zoe Gobeille, Dabney Asmer, Blake Koceja
article en

Abstract

Universal germline genetic testing (GGT) is increasingly utilized in precision cancer care, including access to approved therapeutics, clinical trial enrollment, early detection or prevention of future cancers, and testing of at-risk family members. There is limited data on this approach in patients from historically underrepresented and underserved populations receiving care at community practices. However, these patients may benefit the most from universal GGT as studies show current GGT guidelines miss ∼50% of patients with pathogenic germline variants (PGVs), particularly among Black/African-American patients.

Genetics in Medicine OpenVol. 3
Community Care (US), The US Oncology Network (US), Invitae (United States) (US)
Openalex Percentile: Top 94%
BRCA gene mutations in cancer
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