Literature DB >> 27773374

Barriers to genetic testing in newly diagnosed breast cancer patients: Do surgeons limit testing?

Laura Hafertepen1, Alyssa Pastorino2, Nichole Morman2, Jennifer Snow2, Deepa Halaharvi2, Lindsey Byrne2, Mark Cripe2.   

Abstract

BACKGROUND: Genetic testing results influence treatment recommendations in newly diagnosed breast cancer patients. However, at-risk patients do not uniformly undergo genetic testing. The goal of this study was to identify barriers to genetic testing in newly diagnosed breast cancer patients.
METHODS: A prospective database of newly diagnosed breast cancer patients meeting specific criteria over an 18-month period was created and retrospectively reviewed.
RESULTS: A total of 532 patients were identified at risk for genetic mutation. Of these 313 (59%) patients completed a genetic counseling appointment and 292 (55%) underwent genetic testing. One hundred seven (24%) were never referred to genetic counselors and 89 (17%) were referred but did not complete an appointment. Patients referred to genetics were younger than the nonreferred patients (50.9 vs 60.6 years, P < .001). The 89 women referred to genetics who did not complete an appointment were surveyed and had varied reasons for not completing an appointment.
CONCLUSIONS: The largest barrier to genetic testing was lack of physician referral; therefore, provider education must be improved. Appointments should be convenient and providers should proactively discuss the significant implications of testing results.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  BRCA1; BRCA2; Breast cancer; Genetic counseling; Genetic testing

Mesh:

Year:  2016        PMID: 27773374     DOI: 10.1016/j.amjsurg.2016.08.012

Source DB:  PubMed          Journal:  Am J Surg        ISSN: 0002-9610            Impact factor:   2.565


  8 in total

1.  Predictors of genetic testing uptake in newly diagnosed breast cancer patients.

Authors:  Mary K Ladd; Beth N Peshkin; Claudine Isaacs; Gillian Hooker; Shawna Willey; Heiddis Valdimarsdottir; Tiffani DeMarco; Suzanne O'Neill; Savannah Binion; Marc D Schwartz
Journal:  J Surg Oncol       Date:  2020-04-28       Impact factor: 3.454

2.  Stakeholder Perspectives on Overcoming Barriers to Cascade Testing in Lynch Syndrome: A Qualitative Study.

Authors:  Swetha Srinivasan; Heather Hampel; Jennifer Leeman; Amit Patel; Alanna Kulchak Rahm; Daniel S Reuland; Megan C Roberts
Journal:  Cancer Prev Res (Phila)       Date:  2020-07-29

3.  Recommendation and Acceptance of Counselling for Familial Cancer Risk in Newly Diagnosed Breast Cancer Cases.

Authors:  Karin Kast; Julia Häfner; Evelin Schröck; Arne Jahn; Carmen Werner; Cornelia Meisel; Pauline Wimberger
Journal:  Breast Care (Basel)       Date:  2021-06-17       Impact factor: 2.268

4.  Randomized trial of proactive rapid genetic counseling versus usual care for newly diagnosed breast cancer patients.

Authors:  Marc D Schwartz; Beth N Peshkin; Claudine Isaacs; Shawna Willey; Heiddis B Valdimarsdottir; Rachel Nusbaum; Gillian Hooker; Suzanne O'Neill; Lina Jandorf; Scott P Kelly; Jessica Heinzmann; Aliza Zidell; Katia Khoury
Journal:  Breast Cancer Res Treat       Date:  2018-04-02       Impact factor: 4.872

5.  Systematic development of a training program for healthcare professionals to improve communication about breast cancer genetic counseling with low health literate patients.

Authors:  Jeanine A M van der Giessen; Margreet G E M Ausems; Maria E T C van den Muijsenbergh; Sandra van Dulmen; Mirjam P Fransen
Journal:  Fam Cancer       Date:  2020-10       Impact factor: 2.375

6.  Communication about breast cancer genetic counseling with patients with limited health literacy or a migrant background: evaluation of a training program for healthcare professionals.

Authors:  Jeanine van der Giessen; Mirjam P Fransen; Peter Spreeuwenberg; Mary Velthuizen; Sandra van Dulmen; Margreet G E M Ausems
Journal:  J Community Genet       Date:  2020-12-15

7.  Written pretest information and germline BRCA1/2 pathogenic variant testing in unselected breast cancer patients: predictors of testing uptake.

Authors:  Martin P Nilsson; Erik D Nilsson; Barbro Silfverberg; Åke Borg; Niklas Loman
Journal:  Genet Med       Date:  2018-06-06       Impact factor: 8.822

8.  Development of a plain-language guide for discussing breast cancer genetic counseling and testing with patients with limited health literacy.

Authors:  J A M van der Giessen; M G E M Ausems; E van Riel; A de Jong; M P Fransen; S van Dulmen
Journal:  Support Care Cancer       Date:  2020-10-01       Impact factor: 3.603

  8 in total

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