TY - JOUR
T1 - Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibility
AU - Bradbury, Angela R.
AU - Patrick-Miller, Linda
AU - Long, Jessica
AU - Powers, Jacquelyn
AU - Stopfer, Jill
AU - Forman, Andrea
AU - Rybak, Christina
AU - Mattie, Kristin
AU - Brandt, Amanda
AU - Chambers, Rachelle
AU - Chung, Wendy K.
AU - Churpek, Jane
AU - Daly, Mary B.
AU - Digiovanni, Laura
AU - Farengo-Clark, Dana
AU - Fetzer, Dominique
AU - Ganschow, Pamela
AU - Grana, Generosa
AU - Gulden, Cassandra
AU - Hall, Michael
AU - Kohler, Lynne
AU - Maxwell, Kara
AU - Merrill, Shana
AU - Montgomery, Susan
AU - Mueller, Rebecca
AU - Nielsen, Sarah
AU - Olopade, Olufunmilayo
AU - Rainey, Kimberly
AU - Seelaus, Christina
AU - Nathanson, Katherine L.
AU - Domchek, Susan M.
N1 - Publisher Copyright:
© 2015 American College of Medical Genetics and Genomics.
PY - 2015/6/4
Y1 - 2015/6/4
N2 - 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.
AB - 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.
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U2 - 10.1038/gim.2014.134
DO - 10.1038/gim.2014.134
M3 - Article
C2 - 25297947
SN - 1098-3600
VL - 17
SP - 485
EP - 492
JO - Genetics in Medicine
JF - Genetics in Medicine
IS - 6
ER -