Prospective Feasibility Trial of a Novel Strategy of Facilitated Cascade Genetic Testing Using Telephone Counseling.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
01 05 2020
Historique:
pubmed: 11 1 2020
medline: 2 2 2021
entrez: 11 1 2020
Statut: ppublish

Résumé

Probands with newly diagnosed cancer-associated pathogenic variants were offered facilitated cascade testing whereby the genetics team identified and contacted ARRs by telephone to disclose the familial pathogenic variant and offer telephone counseling and mailed saliva testing. Results and guideline-based recommendations were reviewed by telephone and shared with the primary care physician. Thirty probands were enrolled, and 114 ARRs were identified. Twelve ARRs were excluded (lived outside of the United States, n = 5; proband did not approve of contact, n = 7). Among 102 ARRs telephoned, contact was established with 95 (93%). Among 114 identified ARRs, 66 (58%) completed genetic testing. Among those completing testing, 27 (41%) carried the familial pathogenic variant. Surveys of ARRs at the time of genetic testing and 6 months later demonstrated low levels of anxiety, depression, distress, and uncertainty and high levels of satisfaction with testing. At 6 months, 7 ARRs with pathogenic variants had undergone cancer surveillance interventions and 4 had undergone cancer risk-reducing surgery. Facilitated cascade testing with telephone genetic counseling and mailed saliva kits resulted in high testing uptake among ARRs. Positive genetic testing resulted in utilization of genetically targeted primary disease prevention at short-term follow-up. Facilitated cascade testing is a straightforward, low-cost, easily implemented strategy with significant potential to promote early detection for affected ARRs and reduce cancer mortality and should be evaluated in larger scale clinical trials.

Identifiants

pubmed: 31922918
doi: 10.1200/JCO.19.02005
pmc: PMC7193751
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

1389-1397

Subventions

Organisme : NCI NIH HHS
ID : K07 CA216326
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn

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Auteurs

Melissa K Frey (MK)

Weill Cornell Medicine, New York, NY.

Ryan M Kahn (RM)

Weill Cornell Medicine, New York, NY.

Eloise Chapman-Davis (E)

Weill Cornell Medicine, New York, NY.

Francesca Tubito (F)

Weill Cornell Medicine, New York, NY.

Maira Pires (M)

Weill Cornell Medicine, New York, NY.

Paul Christos (P)

Weill Cornell Medicine, New York, NY.

Samantha Anderson (S)

Weill Cornell Medicine, New York, NY.

Semanti Mukherjee (S)

Memorial Sloan Kettering Cancer, New York, NY.

Bailey Jordan (B)

Weill Cornell Medicine, New York, NY.

Stephanie V Blank (SV)

Memorial Sloan Kettering Cancer, New York, NY.

Thomas A Caputo (TA)

Weill Cornell Medicine, New York, NY.

Ravi N Sharaf (RN)

Weill Cornell Medicine, New York, NY.

Kenneth Offit (K)

Memorial Sloan Kettering Cancer, New York, NY.

Kevin Holcomb (K)

Weill Cornell Medicine, New York, NY.

Steven Lipkin (S)

Weill Cornell Medicine, New York, NY.

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Classifications MeSH