Literature DB >> 32639074

Update on multi-gene panel testing and communication of genetic test results.

Sonya Reid1, Tuya Pal1.   

Abstract

With technological advances, multi-gene panel testing has become increasingly used to identify patients at risk for hereditary breast cancer (HBC). There are currently evidence-based interventions and breast cancer screening strategies that exist for cancer prevention and early detection among patients with HBC. Moreover, in addition to the personal impact of identifying HBC, this information may be shared with at-risk family members to amplify the benefits of testing and subsequent care among those at high risk. Opportunities and challenges with the utilization of updated multi-gene panel testing for HBC, including: (a) tumor sequencing with germline consequences; (b) genetic counseling implications; and (c) strategies to improve the communication of genetic test results to family members will be reviewed. With the advances and expansion of genetic testing, all health care providers need to be updated on both the importance and complexities of HBC counseling and testing, in order to optimize patient care.
© 2020 Wiley Periodicals LLC.

Entities:  

Keywords:  zzm321990BRCAzzm321990; hereditary breast cancer; multi-gene panel; next-generation sequencing; tumor-based testing

Mesh:

Year:  2020        PMID: 32639074      PMCID: PMC7484453          DOI: 10.1111/tbj.13971

Source DB:  PubMed          Journal:  Breast J        ISSN: 1075-122X            Impact factor:   2.431


  49 in total

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Review 3.  Germline Genetic Testing for Breast Cancer Risk: The Past, Present, and Future.

Authors:  Siddhartha Yadav; Fergus J Couch
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Review 4.  Gene panel testing for inherited cancer risk.

Authors:  Michael J Hall; Andrea D Forman; Robert Pilarski; Georgia Wiesner; Veda N Giri
Journal:  J Natl Compr Canc Netw       Date:  2014-09       Impact factor: 11.908

5.  Meta-analysis of BRCA1 and BRCA2 penetrance.

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Journal:  J Clin Oncol       Date:  2007-04-10       Impact factor: 44.544

6.  Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.

Authors:  Freddie Bray; Jacques Ferlay; Isabelle Soerjomataram; Rebecca L Siegel; Lindsey A Torre; Ahmedin Jemal
Journal:  CA Cancer J Clin       Date:  2018-09-12       Impact factor: 508.702

7.  Comparison of Breast Cancer Molecular Features and Survival by African and European Ancestry in The Cancer Genome Atlas.

Authors:  Dezheng Huo; Hai Hu; Suhn K Rhie; Eric R Gamazon; Andrew D Cherniack; Jianfang Liu; Toshio F Yoshimatsu; Jason J Pitt; Katherine A Hoadley; Melissa Troester; Yuanbin Ru; Tara Lichtenberg; Lori A Sturtz; Carl S Shelley; Christopher C Benz; Gordon B Mills; Peter W Laird; Craig D Shriver; Charles M Perou; Olufunmilayo I Olopade
Journal:  JAMA Oncol       Date:  2017-12-01       Impact factor: 31.777

8.  Assessment of interactions between 205 breast cancer susceptibility loci and 13 established risk factors in relation to breast cancer risk, in the Breast Cancer Association Consortium.

Authors:  Pooja Middha Kapoor; Sara Lindström; Sabine Behrens; Xiaoliang Wang; Kyriaki Michailidou; Manjeet K Bolla; Qin Wang; Joe Dennis; Alison M Dunning; Paul D P Pharoah; Marjanka K Schmidt; Peter Kraft; Montserrat García-Closas; Douglas F Easton; Roger L Milne; Jenny Chang-Claude
Journal:  Int J Epidemiol       Date:  2020-02-01       Impact factor: 7.196

9.  Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers.

Authors:  Karoline B Kuchenbaecker; John L Hopper; Daniel R Barnes; Kelly-Anne Phillips; Thea M Mooij; Marie-José Roos-Blom; Sarah Jervis; Flora E van Leeuwen; Roger L Milne; Nadine Andrieu; David E Goldgar; Mary Beth Terry; Matti A Rookus; Douglas F Easton; Antonis C Antoniou; Lesley McGuffog; D Gareth Evans; Daniel Barrowdale; Debra Frost; Julian Adlard; Kai-Ren Ong; Louise Izatt; Marc Tischkowitz; Ros Eeles; Rosemarie Davidson; Shirley Hodgson; Steve Ellis; Catherine Nogues; Christine Lasset; Dominique Stoppa-Lyonnet; Jean-Pierre Fricker; Laurence Faivre; Pascaline Berthet; Maartje J Hooning; Lizet E van der Kolk; Carolien M Kets; Muriel A Adank; Esther M John; Wendy K Chung; Irene L Andrulis; Melissa Southey; Mary B Daly; Saundra S Buys; Ana Osorio; Christoph Engel; Karin Kast; Rita K Schmutzler; Trinidad Caldes; Anna Jakubowska; Jacques Simard; Michael L Friedlander; Sue-Anne McLachlan; Eva Machackova; Lenka Foretova; Yen Y Tan; Christian F Singer; Edith Olah; Anne-Marie Gerdes; Brita Arver; Håkan Olsson
Journal:  JAMA       Date:  2017-06-20       Impact factor: 56.272

10.  Expanded Gene Panel Use for Women With Breast Cancer: Identification and Intervention Beyond Breast Cancer Risk.

Authors:  Erin O'Leary; Daniela Iacoboni; Jennifer Holle; Scott T Michalski; Edward D Esplin; Shan Yang; Karen Ouyang
Journal:  Ann Surg Oncol       Date:  2017-08-01       Impact factor: 5.344

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Journal:  Oncologist       Date:  2021-09-08

Review 2.  Experiences of individuals with a variant of uncertain significance on genetic testing for hereditary cancer risks: a mixed method systematic review.

Authors:  Danielle Gould; Rachel Walker; Grace Makari-Judson; Memnun Seven
Journal:  J Community Genet       Date:  2022-07-12

Review 3.  Fetal nuchal edema and developmental anomalies caused by gene mutations in mice.

Authors:  Akira Sugiyama; Masanori Hirashima
Journal:  Front Cell Dev Biol       Date:  2022-08-30

4.  Spectrum and management of breast cancer patients with variant of uncertain significance mutations at a tertiary care centre in North India.

Authors:  Abhenil Mittal; S V S Deo; Ajay Gogia; Atul Batra; Akash Kumar; Sandeep Bhoriwal; Koushik Sinha Deb; Ekta Dhamija; V L Ramprasad; Olufunmilayo Olopade; Raja Pramanik
Journal:  Ecancermedicalscience       Date:  2022-08-01
  4 in total

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