Speaking genomics to parents offered germline testing for cancer predisposition: Use of a 2-visit consent model.


Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
15 07 2019
Historique:
received: 26 12 2018
revised: 22 02 2019
accepted: 24 02 2019
pubmed: 23 3 2019
medline: 9 4 2020
entrez: 23 3 2019
Statut: ppublish

Résumé

Patients with cancer are increasingly offered genomic sequencing, including germline testing for cancer predisposition or other disorders. Such testing is unfamiliar to patients and families, and clear communication is needed to introduce genomic concepts and convey risk and benefit information. Parents of children with cancer were offered the opportunity to have their children's tumor and germline examined with clinical genomic sequencing. Families were introduced to the study with a 2-visit informed consent model. Baseline genetic knowledge and self-reported literacy/numeracy were collected before a study introduction visit, during which basic concepts related to genomic sequencing were discussed. Information was reinforced during a second visit, during which informed consent was obtained and a posttest was administered. As reflected by the percentage of correct answers on the pretest and posttest assessments, this model increased genetic knowledge by 11.1% (from 77.8% to 88.9%; P < .0001) in 121 parents participating in both the study introduction and consent visits. The percentage of parents correctly identifying the meaning of somatic and germline mutations increased significantly (from 18% to 59% [somatic] and from 31% to 64% [germline]; P < .0001). Nevertheless, these concepts remained unfamiliar to one-third of the parents. No relation was identified between the change in the overall percentage of correct answers and self-reported literacy, numeracy, or demographics. The use of a 2-visit communication model improved knowledge of concepts relevant to genomic sequencing, particularly differences between somatic and germline testing; however, these areas remained confusing to many participants, and reinforcement may be necessary to achieve complete understanding.

Sections du résumé

BACKGROUND
Patients with cancer are increasingly offered genomic sequencing, including germline testing for cancer predisposition or other disorders. Such testing is unfamiliar to patients and families, and clear communication is needed to introduce genomic concepts and convey risk and benefit information.
METHODS
Parents of children with cancer were offered the opportunity to have their children's tumor and germline examined with clinical genomic sequencing. Families were introduced to the study with a 2-visit informed consent model. Baseline genetic knowledge and self-reported literacy/numeracy were collected before a study introduction visit, during which basic concepts related to genomic sequencing were discussed. Information was reinforced during a second visit, during which informed consent was obtained and a posttest was administered.
RESULTS
As reflected by the percentage of correct answers on the pretest and posttest assessments, this model increased genetic knowledge by 11.1% (from 77.8% to 88.9%; P < .0001) in 121 parents participating in both the study introduction and consent visits. The percentage of parents correctly identifying the meaning of somatic and germline mutations increased significantly (from 18% to 59% [somatic] and from 31% to 64% [germline]; P < .0001). Nevertheless, these concepts remained unfamiliar to one-third of the parents. No relation was identified between the change in the overall percentage of correct answers and self-reported literacy, numeracy, or demographics.
CONCLUSIONS
The use of a 2-visit communication model improved knowledge of concepts relevant to genomic sequencing, particularly differences between somatic and germline testing; however, these areas remained confusing to many participants, and reinforcement may be necessary to achieve complete understanding.

Identifiants

pubmed: 30901077
doi: 10.1002/cncr.32071
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2455-2464

Informations de copyright

© 2019 American Cancer Society.

Auteurs

Liza-Marie Johnson (LM)

Division of Quality of Life and Palliative Care, St. Jude Children's Research Hospital, Memphis, Tennessee.

April D Sykes (AD)

Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee.

Zhaohua Lu (Z)

Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee.

Jessica M Valdez (JM)

Department of Pediatric Hematology-Oncology, University of New Mexico Health Science Center, Albuquerque, New Mexico.

Jami Gattuso (J)

Division of Nursing Research, St. Jude Children's Research Hospital, Memphis, Tennessee.

Elsie Gerhardt (E)

Division of Cancer Predisposition, St. Jude Children's Research Hospital, Memphis, Tennessee.

Kayla V Hamilton (KV)

Division of Cancer Predisposition, St. Jude Children's Research Hospital, Memphis, Tennessee.

Lynn W Harrison (LW)

Division of Cancer Predisposition, St. Jude Children's Research Hospital, Memphis, Tennessee.

Stacy J Hines-Dowell (SJ)

Division of Cancer Predisposition, St. Jude Children's Research Hospital, Memphis, Tennessee.

Niki Jurbergs (N)

Division of Psychology, St. Jude Children's Research Hospital, Memphis, Tennessee.

Rose B McGee (RB)

Division of Cancer Predisposition, St. Jude Children's Research Hospital, Memphis, Tennessee.

Regina Nuccio (R)

Division of Cancer Predisposition, St. Jude Children's Research Hospital, Memphis, Tennessee.

Annastasia A Ouma (AA)

Division of Cancer Predisposition, St. Jude Children's Research Hospital, Memphis, Tennessee.

Michele Pritchard (M)

Division of Nursing Research, St. Jude Children's Research Hospital, Memphis, Tennessee.

Emily A Quinn (EA)

Human Genetics and Genetic Counseling Program, Keck Graduate Institute, Claremont, California.

Justin N Baker (JN)

Division of Quality of Life and Palliative Care, St. Jude Children's Research Hospital, Memphis, Tennessee.

Belinda N Mandrell (BN)

Division of Nursing Research, St. Jude Children's Research Hospital, Memphis, Tennessee.

Kim E Nichols (KE)

Division of Cancer Predisposition, St. Jude Children's Research Hospital, Memphis, Tennessee.

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