遗传性癌症风险的多基因检测 - Suppr

Suppr

超能文献

Multigene Panel Testing for Hereditary Cancer Risk.

作者信息

Grissom Alyssa A, Friend Patricia J

机构信息

Loyola University Chicago, Marcella Niehoff School of Nursing, Chicago, Illinois.

出版信息

J Adv Pract Oncol. 2016 May-Jun;7(4):394-407. Epub 2016 May 1.

PMID:29225998

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5679029/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d556/5679029/70591fb7d265/jadp-07-394-g01.jpg

相似文献

Multigene Panel Testing for Hereditary Cancer Risk.

J Adv Pract Oncol. 2016 May-Jun;7(4):394-407. Epub 2016 May 1.

Multigene Panel Testing Detects Equal Rates of Pathogenic BRCA1/2 Mutations and has a Higher Diagnostic Yield Compared to Limited BRCA1/2 Analysis Alone in Patients at Risk for Hereditary Breast Cancer.

Ann Surg Oncol. 2015 Oct;22(10):3282-8. doi: 10.1245/s10434-015-4754-2. Epub 2015 Jul 29.

Germline multigene panel testing revealed a pathogenic variant in a patient with suspected Lynch syndrome.

Int Cancer Conf J. 2020 Oct 9;10(1):6-10. doi: 10.1007/s13691-020-00449-9. eCollection 2021 Jan.

Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment.

JAMA Oncol. 2015 Oct;1(7):943-51. doi: 10.1001/jamaoncol.2015.2690.

Mutation prevalence tables for hereditary cancer derived from multigene panel testing.

Hum Mutat. 2020 Aug;41(8):e1-e6. doi: 10.1002/humu.24053. Epub 2020 Jul 9.

Initial Results of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer and Lynch Syndrome.

Am Surg. 2015 Oct;81(10):941-4.

Multigene Panel Testing for Hereditary Cancer and Genetic Counseling.

Adv Exp Med Biol. 2021;1187:455-471. doi: 10.1007/978-981-32-9620-6_24.

Collaborative Group of the Americas on Inherited Gastrointestinal Cancer Position statement on multigene panel testing for patients with colorectal cancer and/or polyposis.

Fam Cancer. 2020 Jul;19(3):223-239. doi: 10.1007/s10689-020-00170-9.

The Cost-Effectiveness of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer in Norway.

MDM Policy Pract. 2019 Feb 1;4(1):2381468318821103. doi: 10.1177/2381468318821103. eCollection 2019 Jan-Jun.

Development and validation of next generation sequencing based 35-gene hereditary cancer panel.

Hered Cancer Clin Pract. 2020 Apr 28;18:9. doi: 10.1186/s13053-020-00141-2. eCollection 2020.

引用本文的文献

Understanding how gene-disease relationships can impact clinical utility: adaptations and challenges in hereditary cancer testing.

Genome Med. 2025 Jul 1;17(1):73. doi: 10.1186/s13073-025-01499-5.

Multiple cancer susceptible genes sequencing in BRCA-negative breast cancer with high hereditary risk.

Ann Transl Med. 2020 Nov;8(21):1417. doi: 10.21037/atm-20-2999.

The Community Oncology and Academic Medical Center Alliance in the Age of Precision Medicine: Cancer Genetics and Genomics Considerations.

J Clin Med. 2020 Jul 6;9(7):2125. doi: 10.3390/jcm9072125.

本文引用的文献

Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015.

J Natl Compr Canc Netw. 2016 Feb;14(2):153-62. doi: 10.6004/jnccn.2016.0018.

American Society of Clinical Oncology Policy Statement Update: Genetic and Genomic Testing for Cancer Susceptibility.

J Clin Oncol. 2015 Nov 1;33(31):3660-7. doi: 10.1200/JCO.2015.63.0996. Epub 2015 Aug 31.

Do Health Professionals Need Additional Competencies for Stratified Cancer Prevention Based on Genetic Risk Profiling?

J Pers Med. 2015 Jun 9;5(2):191-212. doi: 10.3390/jpm5020191.

Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk.

J Clin Oncol. 2015 Feb 1;33(4):319-25. doi: 10.1200/JCO.2014.57.8088. Epub 2014 Dec 15.

Next-generation sequencing in clinical oncology: next steps towards clinical validation.

Cancers (Basel). 2014 Nov 18;6(4):2296-312. doi: 10.3390/cancers6042296.

Clinical integration of next generation sequencing: coverage and reimbursement challenges.

J Law Med Ethics. 2014 Fall;42 Suppl 1(Suppl 1):22-41. doi: 10.1111/jlme.12160.

Regulation of next generation sequencing.

J Law Med Ethics. 2014 Fall;42 Suppl 1:9-21. doi: 10.1111/jlme.12159.

Gene panel testing for inherited cancer risk.

J Natl Compr Canc Netw. 2014 Sep;12(9):1339-46. doi: 10.6004/jnccn.2014.0128.

Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice.

Fam Cancer. 2014 Dec;13(4):527-36. doi: 10.1007/s10689-014-9741-4.

The evolution of cancer risk assessment in the era of next generation sequencing.

J Genet Couns. 2014 Aug;23(4):633-9. doi: 10.1007/s10897-014-9714-7. Epub 2014 Apr 24.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验