Primary Care Implications of the Expanded National Guidelines for Germline Testing of Patients Previously Diagnosed with Colorectal Cancer

被引:2
|
作者
Sorscher, Steven
机构
[1] Winston-Salem, 27104, NC
关键词
Colorectal Cancer; Genetic Testing; Germline Mutation; Primary Health Care; Risk Assessment; SUSCEPTIBILITY GENE-MUTATIONS; SURVIVORSHIP CARE; BREAST-CANCER; PREVENTION; PROVIDERS;
D O I
10.3122/jabfm.2022.220288R1
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Colorectal cancer (CRC) is among the most common cancers diagnosed in the United States. Most patients are cured, have completed their routine surveillance in oncology clinics, and are being followed by primary care clinicians (PCCs). Those providers are tasked with discussing with these patients genetic testing for inherited cancer-predisposing genes that are called PGVs. Recently, the National Comprehensive Cancer Network (NCCN) Hereditary/Familial High-Risk Assessment: Colorectal Guidelines expert panel updated their recommendations for genetic testing. It is now recommended that all patients diagnosed with CRC before age 50 be tested and patients diagnosed at age 50 or older be considered for multigene panel testing (MGPT) for inherited cancer-predisposing PGVs. Here, I discuss the basis for the NCCN expanded genetic testing recommendations and highlight the salient controversies related to genetic testing. I also review the literature that suggests that PCCs identified more training as the measure needed before they are comfortable having complex discussions related to genetic testing with their patients.
引用
收藏
页码:360 / 365
页数:6
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