H Hampel, MB Yurgelun - Journal of Clinical Oncology, 2022 - ascopubs.org
Use of germline genetic testing among patients with cancer is increasing because of (1) the availability of multigene panel tests that include multiple cancer susceptibility genes in a …
I Bedrosian, MR Somerfield, MI Achatz… - Journal of Clinical …, 2024 - ascopubs.org
PURPOSE To develop recommendations for germline mutation testing for patients with breast cancer. METHODS An ASCO–Society of Surgical Oncology (SSO) panel convened to …
ED Esplin, SM Nielsen, SL Bristow, JE Garber… - JCO Precision …, 2022 - ascopubs.org
Historically, professional society guidelines have recommended limited genetic testing for hereditary cancer syndromes (HCS) to patients with cancer thought to be at highest risk for …
YL Liu, A Maio, Y Kemel, EE Salo‐Mullen… - Cancer, 2022 - Wiley Online Library
Background Germline risk assessment is increasing as part of cancer care; however, disparities in subsequent genetic counseling are unknown. Methods Pan‐cancer patients …
Many countries currently invest in technologies and data infrastructures to foster precision medicine (PM), which is hoped to better tailor disease treatment and prevention to individual …
J Limoges, P Chiu, D Dordunoo… - JBI Evidence …, 2024 - journals.lww.com
Objective: The objective of this review was to map the available global evidence on strategies that nurses can use to facilitate genomics-informed health care to address health …
QY Zhu, ZM He, WM Cao, B Li - Frontiers in Oncology, 2023 - frontiersin.org
TSC2 is a tumor suppressor gene as well as a disease-causing gene for autosomal dominant disorder tuberous sclerosis complex (TSC). Research has found that some tumor …
TA Yap, ZK Stadler, LA Stout… - American Society of …, 2023 - ascopubs.org
In the era of precision medicine, genomic interrogation for identification of both germline and somatic genetic alterations has become increasingly important. While such germline testing …
S Makhnoon, B Levin, M Ensinger, K Mattie… - Cancer …, 2023 - Wiley Online Library
Background Clinical interpretation of genetic test results is complicated by variants of uncertain significance (VUS) that have an unknown impact on health but can be clarified …