Parental Preferences Surrounding Timing and Content of Consent Conversations for Clinical Germline Genetic Testing Following a Child's New Cancer Diagnosis.


Journal

JCO precision oncology
ISSN: 2473-4284
Titre abrégé: JCO Precis Oncol
Pays: United States
ID NLM: 101705370

Informations de publication

Date de publication:
10 2022
Historique:
entrez: 20 10 2022
pubmed: 21 10 2022
medline: 25 10 2022
Statut: ppublish

Résumé

Clinical genomic testing is increasingly being used to direct pediatric cancer care. Many centers are interested in offering testing of tumors and paired germline tissues at or near the time of cancer diagnosis. We conducted this study to better understand parent preferences surrounding timing and content of consent conversations for clinical germline genetic testing of their children with cancer as a part of real-time cancer care. A seven-question survey developed by the Division of Cancer Predisposition and collaborators at St Jude Children's Research Hospital (St Jude) was distributed to members of the St Jude Patient Family Advisory Council, which included parents of childhood cancer survivors and bereaved parents whose children with cancer had died. Parents were asked to provide free text comments after each question. Qualitative methods were used to derive codes from parent comments, and survey results were depicted using descriptive statistics. The survey was completed by 172 parents. Ninety-three (54%) endorsed an approach for consent conversations ≥ 1 month after cancer diagnosis, whereas 58 (34%) endorsed an approach at 1-2 weeks and 21 (12%) at 1-2 days. Needing time to adjust to a new or relapsed cancer diagnosis and feeling overwhelmed were frequent themes; however, parents acknowledged the urgency and importance of testing. Parents desired testing of as many cancer-related genes as possible, with clinical utility the most important factor for proceeding with testing. Most parents (75%) desired germline results to be disclosed in person, preferably by a genetic counselor. Parents described urgency and benefits associated with germline testing, but desired flexibility in timing to allow for initial adjustment after their child's cancer diagnosis.

Identifiants

pubmed: 36265116
doi: 10.1200/PO.22.00323
pmc: PMC9848596
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2200323

Subventions

Organisme : NCI NIH HHS
ID : P30 CA021765
Pays : United States

Déclaration de conflit d'intérêts

<b>Liza Marie Johnson</b><b>Research Funding:</b> Crispr Therapeutics (Inst) <b>Kim Nichols</b><b>Stock and Other Ownership Interests:</b> Incyte (I)<b>Research Funding:</b> Incyte/NovartisNo other potential conflicts of interest were reported.

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Auteurs

Belinda N Mandrell (BN)

Division of Nursing Research, Department of Pediatrics, St Jude Children's Research Hospital, Memphis, TN.

Liza Marie Johnson (LM)

Department of Oncology, St Jude Children's Research Hospital, Memphis, TN.

Mary Caples (M)

Division of Nursing Research, Department of Pediatrics, St Jude Children's Research Hospital, Memphis, TN.

Jami Gattuso (J)

Division of Nursing Research, Department of Pediatrics, St Jude Children's Research Hospital, Memphis, TN.

Jamie L Maciaszek (JL)

Department of Pathology, St Jude Children's Research Hospital, Memphis, TN.

Roya Mostafavi (R)

Division of Cancer Predisposition, Department of Oncology, St Jude Children's Research Hospital, Memphis, TN.

Katianne M Howard Sharp (KMH)

Department of Psychology, St Jude Children's Research Hospital, Memphis, TN.

Kim E Nichols (KE)

Division of Cancer Predisposition, Department of Oncology, St Jude Children's Research Hospital, Memphis, TN.

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