Literature DB >> 28434142

Cancer Genetic Counseling and Testing in an Era of Rapid Change.

Gillian W Hooker1, Keelia Rhoads Clemens2, John Quillin3, Kristen J Vogel Postula4, Pia Summerour5, Rebecca Nagy6, Adam H Buchanan7.   

Abstract

The impacts of the Association for Molecular Pathology vs. Myriad Supreme Court decision regarding patenting DNA segments and multi-gene testing on cancer genetic counseling practice have not been well described. We aimed to assess genetic counselors' perceptions of how their genetic testing-related practices for hereditary breast and/or ovarian cancer (HBOC) changed after these events. One-hundred fifty-two genetic counselors from the National Society of Genetic Counselors Cancer Special Interest Group completed an anonymous, online, mixed-methods survey in November 2013. The survey presented four hypothetical patients and asked about changes in testing practice. Across the vignettes, a majority of participants reported specific changes in testing decisions following Association for Molecular Pathology vs. Myriad and availability of multi-gene testing. Ninety-three percent of participants reported changing the types of first- and second-line tests they order for HBOC; the degree of change varied geographically. Qualitative analysis indicated that some counselors have altered the counseling session content, trading depth of information for breadth and spending more time counseling about uncertainty. This study shows that cancer genetic counselors are adapting quickly to genetic testing changes, but with wide variability. Findings suggest future research to elucidate clinicians' and patients' preferences for guidance on the clinical implementation of next-generation sequencing.

Entities:  

Keywords:  BRCA1; BRCA2; Cancer genetic counseling; Cancer genetic testing; Expanded multi-gene panel testing

Mesh:

Year:  2017        PMID: 28434142     DOI: 10.1007/s10897-017-0099-2

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  18 in total

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

Authors:  Heather Fecteau; Kristen J Vogel; Kristen Hanson; Shannon Morrill-Cornelius
Journal:  J Genet Couns       Date:  2014-04-24       Impact factor: 2.537

2.  Multiplex genetic testing for cancer susceptibility: out on the high wire without a net?

Authors:  Susan M Domchek; Angela Bradbury; Judy E Garber; Kenneth Offit; Mark E Robson
Journal:  J Clin Oncol       Date:  2013-03-04       Impact factor: 44.544

3.  Adapting genetic counseling training to the genomic era: more an evolution than a revolution.

Authors:  Catherine Wicklund; Angela Trepanier
Journal:  J Genet Couns       Date:  2014-01-28       Impact factor: 2.537

Review 4.  Next-generation sequencing for inherited breast cancer risk: counseling through the complexity.

Authors:  Irene R Rainville; Huma Q Rana
Journal:  Curr Oncol Rep       Date:  2014-03       Impact factor: 5.075

5.  Are mastectomy rates really increasing in the United States?

Authors:  Elizabeth B Habermann; Andrea Abbott; Helen M Parsons; Beth A Virnig; Waddah B Al-Refaie; Todd M Tuttle
Journal:  J Clin Oncol       Date:  2010-06-14       Impact factor: 44.544

6.  Discussing race-related limitations of genomic testing for colon cancer risk: implications for education and counseling.

Authors:  Morgan N Butrick; Lauren Vanhusen; Kara-Grace Leventhal; Gillian W Hooker; Rachel Nusbaum; Beth N Peshkin; Yasmin Salehizadeh; Jessica Pavlick; Marc D Schwartz; Kristi D Graves
Journal:  Soc Sci Med       Date:  2014-05-15       Impact factor: 4.634

7.  NSGC practice guideline: risk assessment and genetic counseling for hereditary breast and ovarian cancer.

Authors:  Janice L Berliner; Angela Musial Fay; Shelly A Cummings; Brittany Burnett; Todd Tillmanns
Journal:  J Genet Couns       Date:  2012-11-28       Impact factor: 2.537

8.  Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibility.

Authors:  Angela R Bradbury; Linda Patrick-Miller; Jessica Long; Jacquelyn Powers; Jill Stopfer; Andrea Forman; Christina Rybak; Kristin Mattie; Amanda Brandt; Rachelle Chambers; Wendy K Chung; Jane Churpek; Mary B Daly; Laura Digiovanni; Dana Farengo-Clark; Dominique Fetzer; Pamela Ganschow; Generosa Grana; Cassandra Gulden; Michael Hall; Lynne Kohler; Kara Maxwell; Shana Merrill; Susan Montgomery; Rebecca Mueller; Sarah Nielsen; Olufunmilayo Olopade; Kimberly Rainey; Christina Seelaus; Katherine L Nathanson; Susan M Domchek
Journal:  Genet Med       Date:  2014-10-09       Impact factor: 8.822

9.  The integration of next-generation sequencing panels in the clinical cancer genetics practice: an institutional experience.

Authors:  Caitlin B Mauer; Sara M Pirzadeh-Miller; Linda D Robinson; David M Euhus
Journal:  Genet Med       Date:  2013-10-10       Impact factor: 8.822

10.  Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients.

Authors:  Holly LaDuca; A J Stuenkel; Jill S Dolinsky; Steven Keiles; Stephany Tandy; Tina Pesaran; Elaine Chen; Chia-Ling Gau; Erika Palmaer; Kamelia Shoaepour; Divya Shah; Virginia Speare; Stephanie Gandomi; Elizabeth Chao
Journal:  Genet Med       Date:  2014-04-24       Impact factor: 8.822

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  15 in total

Review 1.  Familial/inherited cancer syndrome: a focus on the highly consanguineous Arab population.

Authors:  Fawz S AlHarthi; Alya Qari; Alaa Edress; Malak Abedalthagafi
Journal:  NPJ Genom Med       Date:  2020-02-03       Impact factor: 8.617

2.  High-Risk Palliative Care Patients' Knowledge and Attitudes about Hereditary Cancer Testing and DNA Banking.

Authors:  John M Quillin; Oluwabunmi Emidio; Brittany Ma; Lauryn Bailey; Thomas J Smith; In Guk Kang; Brandon J Yu; Oluwafemi Patrick Owodunni; Mohammed Abusamaan; Rab Razzak; Joann N Bodurtha
Journal:  J Genet Couns       Date:  2017-12-04       Impact factor: 2.537

3.  Genetic testing and eHealth usage among Deaf women.

Authors:  Poorna Kushalnagar; Juliana Holcomb; Georgia R Sadler
Journal:  J Genet Couns       Date:  2019-06-10       Impact factor: 2.537

4.  Mutation Rates in Cancer Susceptibility Genes in Patients With Breast Cancer With Multiple Primary Cancers.

Authors:  Kara N Maxwell; Brandon M Wenz; Abha Kulkarni; Bradley Wubbenhorst; Kurt D'Andrea; Benita Weathers; Noah Goodman; Joseph Vijai; Jenna Lilyquist; Steven N Hart; Thomas P Slavin; Kasmintan A Schrader; Vignesh Ravichandran; Tinu Thomas; Chunling Hu; Mark E Robson; Paolo Peterlongo; Bernardo Bonanni; James M Ford; Judy E Garber; Susan L Neuhausen; Payal D Shah; Angela R Bradbury; Angela M DeMichele; Kenneth Offit; Jeffrey N Weitzel; Fergus J Couch; Susan M Domchek; Katherine L Nathanson
Journal:  JCO Precis Oncol       Date:  2020-08-19

5.  Use and Patient-Reported Outcomes of Clinical Multigene Panel Testing for Cancer Susceptibility in the Multicenter Communication of Genetic Test Results by Telephone Study.

Authors:  Michael J Hall; Linda J Patrick-Miller; Brian L Egleston; Susan M Domchek; Mary B Daly; Pamela Ganschow; Generosa Grana; Olufunmilayo I Olopade; Dominique Fetzer; Amanda Brandt; Rachelle Chambers; Dana F Clark; Andrea Forman; Rikki Gaber; Cassandra Gulden; Janice Horte; Jessica M Long; Terra Lucas; Shreshtha Madaan; Kristin Mattie; Danielle McKenna; Susan Montgomery; Sarah Nielsen; Jacquelyn Powers; Kim Rainey; Christina Rybak; Michelle Savage; Christina Seelaus; Jessica Stoll; Jill E Stopfer; Xinxin Shirley Yao; Angela R Bradbury
Journal:  JCO Precis Oncol       Date:  2018-12-18

6.  Uptake of genetic counseling and multi-gene panel testing among women in the Intermountain West with previous negative BRCA1 and BRCA2 results contacted for updated testing.

Authors:  Ryan Mooney; Whitney Espinel; Ashley Elrick; Kelsey Kehoe; Wendy Kohlmann; Kimberly A Kaphingst
Journal:  J Genet Couns       Date:  2021-09-27       Impact factor: 2.717

7.  Problems of Unknown Significance: Counseling in the Era of Next Generation Sequencing.

Authors:  U Fahrioğlu
Journal:  Balkan J Med Genet       Date:  2018-10-29       Impact factor: 0.519

8.  Population Genomic Screening for Genetic Etiologies of Neurodevelopmental/Psychiatric Disorders Demonstrates Personal Utility and Positive Participant Responses.

Authors:  Karen E Wain; Kasia Tolwinski; Emily Palen; Alexis R Heidlebaugh; Karahlyn Holdren; Lauren Kasparson Walsh; Matthew T Oetjens; David H Ledbetter; Christa Lese Martin
Journal:  J Pers Med       Date:  2021-05-01

9.  The impact of hereditary cancer gene panels on clinical care and lessons learned.

Authors:  Volkan Okur; Wendy K Chung
Journal:  Cold Spring Harb Mol Case Stud       Date:  2017-11-21

Review 10.  Evolution of genetic assessment for BRCA-associated gynaecologic malignancies: a Canadian multisociety roadmap.

Authors:  Jeanna M McCuaig; Tracy L Stockley; Patricia Shaw; Michael Fung-Kee-Fung; Alon D Altman; James Bentley; Marcus Q Bernardini; Beatrice Cormier; Hal Hirte; Katharina Kieser; Andree MacMillan; Wendy S Meschino; Karen Panabaker; Renee Perrier; Diane Provencher; Kasmintan A Schrader; Kimberly Serfas; Eva Tomiak; Nora Wong; Sean S Young; Walter Henri Gotlieb; Paul Hoskins; Raymond H Kim
Journal:  J Med Genet       Date:  2018-07-24       Impact factor: 6.318

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