Challenges adopting next-generation sequencing in community oncology practice

被引:6
作者
Ashbury, Fredrick D. [1 ,2 ,3 ]
Thompson, Keith [1 ,4 ,5 ]
Williams, Casey [6 ,7 ]
Williams, Kirstin [6 ]
机构
[1] VieCure, 4949 South Syracuse St,Suite 450, Denver, CO 80237 USA
[2] Univ Calgary, Dept Oncol, Calgary, AB, Canada
[3] Univ Toronto, Dalla Lana Sch Publ Hlth, Toronto, ON, Canada
[4] Univ Alabama Birmingham, Fac Med, Birmingham, AL USA
[5] Montgomery Canc Ctr, Montgomery, AL USA
[6] Univ South Dakota, Vermillion, SD USA
[7] Avera Canc Inst, Sioux Falls, SD USA
关键词
cancer; genomic sequencing; molecular testing; personalized medicine; physician behaviour; precision oncology;
D O I
10.1097/CCO.0000000000000764
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of review We are in an exhilarating time in which innovations exist to help reduce the impact of cancer for individuals, practitioners and society. Innovative tools in cancer genomics can optimize decision-making concerning appropriate drugs (alone or in combination) to cure or prolong life. The genomic characterization of tumours can also give direction to the development of novel drugs. Next-generation tumour sequencing is increasingly becoming an essential part of clinical decision-making, and, as such, will require appropriate coordination for effective adoption and delivery. Recent findings There are several challenges that will need to be addressed if we are to facilitate cancer genomics as part of routine community oncology practice. Recent research into this novel testing paradigm has demonstrated the barriers are at the individual level, while others are at the institution and societal levels. This article, based on the authors' experience in community oncology practice and summary of literature, describes these challenges so strategies can be developed to address these challenges to improve patient outcomes.
引用
收藏
页码:507 / 512
页数:6
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