Literature DB >> 24355094

Communication and technology in genetic counseling for familial cancer.

H T Lynch1, C Snyder, M Stacey, B Olson, S K Peterson, S Buxbaum, T Shaw, P M Lynch.   

Abstract

When a cancer predisposing germline mutation is detected in an index case, the presence of the underlying syndrome is confirmed and the potential for predictive testing of at-risk relatives is established. However, the reporting of a positive family history does not routinely lead to communication of information about risk to close, much less distant relatives. This review summarizes information technology utilized to address penetration or 'reach' of knowledge of risk within extended families, including the use of telephone and video counseling to reach distant patients, and anticipate novel internet-based processes for communication between investigators and relatives.
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  Lynch syndrome; colorectal cancer; familial cancer; genetic counseling; genetic testing; hereditary cancer; hereditary non-polyposis colorectal cancer; information technology

Mesh:

Year:  2013        PMID: 24355094      PMCID: PMC4371849          DOI: 10.1111/cge.12317

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  53 in total

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Journal:  Int J Cancer       Date:  2000-01-20       Impact factor: 7.396

2.  Delivery of Internet-based cancer genetic counselling services to patients' homes: a feasibility study.

Authors:  Neal J Meropol; Mary B Daly; Hetal S Vig; Frank J Manion; Sharon L Manne; Carla Mazar; Camara Murphy; Nicholas Solarino; Vadim Zubarev
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3.  Surveillance colonoscopy improves survival in a cohort of subjects with a single mismatch repair gene mutation.

Authors:  D A Stupart; P A Goldberg; U Algar; R Ramesar
Journal:  Colorectal Dis       Date:  2009-02       Impact factor: 3.788

4.  Genetic uptake in BRCA-mutation families is related to emotional and behavioral communication characteristics of index patients.

Authors:  Karin Landsbergen; Chris Verhaak; Floor Kraaimaat; Nicoline Hoogerbrugge
Journal:  Fam Cancer       Date:  2005       Impact factor: 2.375

5.  An interactive computer program can effectively educate patients about genetic testing for breast cancer susceptibility.

Authors:  M J Green; B B Biesecker; A M McInerney; D Mauger; N Fost
Journal:  Am J Med Genet       Date:  2001-09-15

6.  Education about genetic testing for breast cancer susceptibility: patient preferences for a computer program or genetic counselor.

Authors:  M J Green; A M McInerney; B B Biesecker; N Fost
Journal:  Am J Med Genet       Date:  2001-09-15

7.  Health benefits and cost-effectiveness of primary genetic screening for Lynch syndrome in the general population.

Authors:  Tuan A Dinh; Benjamin I Rosner; James C Atwood; C Richard Boland; Sapna Syngal; Hans F A Vasen; Stephen B Gruber; Randall W Burt
Journal:  Cancer Prev Res (Phila)       Date:  2010-11-18

8.  BRCA1/2 predictive testing: a study of uptake in two centres.

Authors:  Lucy Brooks; Fiona Lennard; Andrew Shenton; Fiona Lalloo; Ingrid Ambus; Audrey Ardern-Jones; Rachel Belk; Bronwyn Kerr; David Craufurd; Rosalind Eeles; D Gareth Evans
Journal:  Eur J Hum Genet       Date:  2004-08       Impact factor: 4.246

Review 9.  Guidelines for disclosing genetic information to family members: from development to use.

Authors:  Béatrice Godard; Thierry Hurlimann; Martin Letendre; Nathalie Egalité
Journal:  Fam Cancer       Date:  2006       Impact factor: 2.375

10.  The interface of Medicare coverage decision-making and emerging molecular-based laboratory testing.

Authors:  Mitchell I Burken; Kathleen S Wilson; Karen Heller; Victoria M Pratt; Michele M Schoonmaker; Eric Seifter
Journal:  Genet Med       Date:  2009-04       Impact factor: 8.822

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  9 in total

1.  Promoting guideline-based cancer genetic risk assessment for hereditary breast and ovarian cancer in ethnically and geographically diverse cancer survivors: Rationale and design of a 3-arm randomized controlled trial.

Authors:  Anita Y Kinney; Rachel Howell; Rachel Ruckman; Jean A McDougall; Tawny W Boyce; Belinda Vicuña; Ji-Hyun Lee; Dolores D Guest; Randi Rycroft; Patricia A Valverde; Kristina M Gallegos; Angela Meisner; Charles L Wiggins; Antoinette Stroup; Lisa E Paddock; Scott T Walters
Journal:  Contemp Clin Trials       Date:  2018-09-18       Impact factor: 2.226

Review 2.  Milestones of Lynch syndrome: 1895-2015.

Authors:  Henry T Lynch; Carrie L Snyder; Trudy G Shaw; Christopher D Heinen; Megan P Hitchins
Journal:  Nat Rev Cancer       Date:  2015-02-12       Impact factor: 60.716

3.  Patient Perceptions of Telephone vs. In-Person BRCA1/BRCA2 Genetic Counseling.

Authors:  Beth N Peshkin; Scott Kelly; Rachel H Nusbaum; Morgan Similuk; Tiffani A DeMarco; Gillian W Hooker; Heiddis B Valdimarsdottir; Andrea D Forman; Jessica Rispoli Joines; Claire Davis; Shelley R McCormick; Wendy McKinnon; Kristi D Graves; Claudine Isaacs; Judy Garber; Marie Wood; Lina Jandorf; Marc D Schwartz
Journal:  J Genet Couns       Date:  2015-10-12       Impact factor: 2.537

4.  Quantifying family dissemination and identifying barriers to communication of risk information in Australian BRCA families.

Authors:  Emma Healey; Natalie Taylor; Sian Greening; Claire E Wakefield; Linda Warwick; Rachel Williams; Kathy Tucker
Journal:  Genet Med       Date:  2017-05-11       Impact factor: 8.822

Review 5.  Health-care professionals' responsibility to patients' relatives in genetic medicine: a systematic review and synthesis of empirical research.

Authors:  Sandi Dheensa; Angela Fenwick; Shiri Shkedi-Rafid; Gillian Crawford; Anneke Lucassen
Journal:  Genet Med       Date:  2015-06-25       Impact factor: 8.822

6.  Development of a Secure Website to Facilitate Information Sharing in Families at High Risk of Bowel Cancer-The Familyweb Study.

Authors:  Selina Goodman; Heather Skirton; Leigh Jackson; Ray B Jones
Journal:  Cancers (Basel)       Date:  2021-05-16       Impact factor: 6.639

7.  Leveraging Health Information Technology to Collect Family Cancer History: A Systematic Review and Meta-Analysis.

Authors:  Xuan Li; Ryan M Kahn; Noelani Wing; Zhen Ni Zhou; Andreas Ian Lackner; Hannah Krinsky; Nora Badiner; Rhea Fogla; Isabel Wolfe; Hannah Bergeron; Becky Baltich Nelson; Charlene Thomas; Paul J Christos; Ravi N Sharaf; Evelyn Cantillo; Kevin Holcomb; Eloise Chapman-Davis; Melissa K Frey
Journal:  JCO Clin Cancer Inform       Date:  2021-06

8.  Utilization of health information technology among cancer genetic counselors.

Authors:  Jordon B Ritchie; Caitlin G Allen; Heath Morrison; Michelle Nichols; Steven D Lauzon; Joshua D Schiffman; Chanita Hughes Halbert; Brandon M Welch
Journal:  Mol Genet Genomic Med       Date:  2020-05-28       Impact factor: 2.183

9.  Pedigree based DNA sequencing pipeline for germline genomes of cancer families.

Authors:  Asta Försti; Abhishek Kumar; Nagarajan Paramasivam; Matthias Schlesner; Calogerina Catalano; Dagmara Dymerska; Jan Lubinski; Roland Eils; Kari Hemminki
Journal:  Hered Cancer Clin Pract       Date:  2016-08-09       Impact factor: 2.857

  9 in total

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