Literature DB >> 32309911

Mainstream consent programs for genetic counseling in cancer patients: A systematic review.

Tahlia Scheinberg1,2,3, Alison Young2,4, Henry Woo2,5, Annabel Goodwin1,6,7, Kate L Mahon1,2,3, Lisa G Horvath1,2,3.   

Abstract

As demand for germline genetic testing for cancer patients increases, novel methods of genetic counseling are required. One such method is the mainstream consent pathway, whereby a member of the oncology team (rather than a genetic specialist) is responsible for counseling, consenting, and arranging genetic testing for cancer patients. We systematically reviewed the literature for evidence evaluating mainstream pathways for patients with breast, ovarian, colorectal, and prostate cancer. Medline, EMBASE, and Cochrane Library were searched for studies that met inclusion and exclusion criteria. Article references were checked for additional studies. Trial databases were searched for ongoing studies. Of the 13 papers that met inclusion criteria, 11 individual study groups were identified (two study groups had two publications each). Ten of the 11 studies evaluated the acceptability, feasibility, and impact of BRCA testing for patients and/or clinicians in different clinical settings in breast and ovarian cancer, while the final study explored the attitudes of colorectal specialists toward genetic testing for colorectal cancer. None involved prostate cancer. Overall, mainstream pathways were acceptable and feasible. Medical oncologist- and nurse-driven pathways were particularly successful, with both patients and clinicians satisfied with this process. Although the content of pretest counseling was less consistent compared with counseling via the traditional model, patients were largely satisfied with the education they received. Further research is required to evaluate the mainstream pathway for men with prostate cancer.
© 2020 John Wiley & Sons Australia, Ltd.

Entities:  

Keywords:  breast neoplasms; colorectal neoplasms; genetic testing; ovarian neoplasms; prostatic neoplasms; service delivery models; systematic review

Mesh:

Year:  2020        PMID: 32309911     DOI: 10.1111/ajco.13334

Source DB:  PubMed          Journal:  Asia Pac J Clin Oncol        ISSN: 1743-7555            Impact factor:   2.601


  6 in total

1.  Mainstreaming germline genetic testing for patients with pancreatic cancer increases uptake.

Authors:  Mitchell L Ramsey; Jewel Tomlinson; Rachel Pearlman; Laith Abushahin; Amber Aeilts; Hui-Zi Chen; Yan Chen; Ashley Compton; Rifat Elkhatib; Levi Geiger; John Hays; Joanne Jeter; Ning Jin; Pannaga Malalur; Sameek Roychowdhury; Jessica Ruple; Jennifer Prebish; Peter P Stanich; Heather Hampel
Journal:  Fam Cancer       Date:  2022-06-17       Impact factor: 2.446

Review 2.  Challenges of Genomic Testing for Hereditary Breast and Ovarian Cancers.

Authors:  Lindsey McAlarnen; Kristen Stearns; Denise Uyar
Journal:  Appl Clin Genet       Date:  2021-01-14

3.  Mainstreaming Genetic Testing for Adult Patients With Autosomal Dominant Polycystic Kidney Disease.

Authors:  Mark D Elliott; Leslie C James; Emily L Simms; Priyana Sharma; Louis P Girard; Kim Cheema; Meghan J Elliott; Julie L Lauzon; Justin Chun
Journal:  Can J Kidney Health Dis       Date:  2021-10-29

Review 4.  The Feasibility of Implementing Mainstream Germline Genetic Testing in Routine Cancer Care-A Systematic Review.

Authors:  Kyra Bokkers; Michiel Vlaming; Ellen G Engelhardt; Ronald P Zweemer; Inge M van Oort; Lambertus A L M Kiemeney; Eveline M A Bleiker; Margreet G E M Ausems
Journal:  Cancers (Basel)       Date:  2022-02-19       Impact factor: 6.639

5.  Mainstream genetic testing for women with ovarian cancer provides a solid basis for patients to make a well-informed decision about genetic testing.

Authors:  Kyra Bokkers; Eveline M A Bleiker; Jacob P Hoogendam; Mary E Velthuizen; Henk W R Schreuder; Cornelis G Gerestein; Joost G Lange; Jacqueline A Louwers; Marco J Koudijs; Margreet G E M Ausems; Ronald P Zweemer
Journal:  Hered Cancer Clin Pract       Date:  2022-09-08       Impact factor: 2.164

6.  Talking about Risk, UncertaintieS of Testing IN Genetics (TRUSTING): development and evaluation of an educational programme for healthcare professionals about BRCA1 & BRCA2 testing.

Authors:  Lesley Fallowfield; Ivonne Solis-Trapala; Rachel Starkings; Shirley May; Lucy Matthews; Diana Eccles; D Gareth Evans; Clare Turnbull; Gillian Crawford; Valerie Jenkins
Journal:  Br J Cancer       Date:  2022-06-17       Impact factor: 9.075

  6 in total

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