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

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 HallLynne Kohler, Kara Maxwell, Shana Merrill, Susan Montgomery, Rebecca Mueller, Sarah Nielsen, Olufunmilayo Olopade, Kimberly Rainey, Christina Seelaus, Katherine L. Nathanson, Susan M. Domchek

Research output: Contribution to journalArticlepeer-review

66 Scopus citations

Abstract

Purpose: Multiplex genetic testing, including both moderate- and high-penetrance genes for cancer susceptibility, is associated with greater uncertainty than traditional testing, presenting challenges to informed consent and genetic counseling. We sought to develop a new model for informed consent and genetic counseling for four ongoing studies. Methods:Drawing from professional guidelines, literature, conceptual frameworks, and clinical experience, a multidisciplinary group developed a tiered-binned genetic counseling approach proposed to facilitate informed consent and improve outcomes of cancer susceptibility multiplex testing. Results: In this model, tier 1 "indispensable" information is presented to all patients. More specific tier 2 information is provided to support variable informational needs among diverse patient populations. Clinically relevant information is "binned" into groups to minimize information overload, support informed decision making, and facilitate adaptive responses to testing. Seven essential elements of informed consent are provided to address the unique limitations, risks, and uncertainties of multiplex testing. Conclusion: A tiered-binned model for informed consent and genetic counseling has the potential to address the challenges of multiplex testing for cancer susceptibility and to support informed decision making and adaptive responses to testing. Future prospective studies including patient-reported outcomes are needed to inform how to best incorporate multiplex testing for cancer susceptibility into clinical practice.

Original languageEnglish
Pages (from-to)485-492
Number of pages8
JournalGenetics in Medicine
Volume17
Issue number6
DOIs
StatePublished - Jun 4 2015

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