Genetic Testing Uptake among Ovarian Cancer Survivors in the Genetic Risk Analysis in Ovarian Cancer (GRACE) Study.

cancer prevention gynecologic cancer risk reduction ovarian cancer

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
17 Jul 2024
Historique:
received: 18 05 2024
revised: 08 07 2024
accepted: 15 07 2024
medline: 27 7 2024
pubmed: 27 7 2024
entrez: 27 7 2024
Statut: epublish

Résumé

Recommendations state all people with ovarian cancers (OCs) receive genetic counseling, but testing uptake is only between 15 and 31%. Those with a prior diagnosis of OC who have not received genetic testing represent a missed opportunity for life-saving genetic risk information. The Genetic Risk Analysis in ovarian CancEr (GRACE) study aimed to evaluate the feasibility of the retrospective identification ("Traceback") of individuals diagnosed with OC. This nonrandomized intervention study within two integrated health care systems identified participants with a history of OC between 1998 and 2020 who did not have genetic testing or testing limited to BRCA1/2. Participants received clinical genomic sequencing via a custom 60 gene panel. This study measured the feasibility of the Traceback methodology in OC survivors. The initial cohort included 929 individuals, of which 57% had no prior genetic testing. Of the 302 eligible for recruitment, 88 consented to participate. We were able to outreach 97% of the eligible population using contact information from medical records. The stage at diagnosis was the only factor associated with consent. Of the 78 who returned their saliva sample, 21% had pathogenic/likely pathogenic variants, and 79% had negative results. The GRACE study resulted in a 29% uptake of genetic testing in OC survivors. The time since diagnosis did not have an impact on consent or ability to contact. GRACE can inform the implementation of future Traceback programs, providing guidance on how to prevent and mitigate the burden of OC and other hereditary cancers.

Sections du résumé

BACKGROUND BACKGROUND
Recommendations state all people with ovarian cancers (OCs) receive genetic counseling, but testing uptake is only between 15 and 31%. Those with a prior diagnosis of OC who have not received genetic testing represent a missed opportunity for life-saving genetic risk information. The Genetic Risk Analysis in ovarian CancEr (GRACE) study aimed to evaluate the feasibility of the retrospective identification ("Traceback") of individuals diagnosed with OC.
METHODS METHODS
This nonrandomized intervention study within two integrated health care systems identified participants with a history of OC between 1998 and 2020 who did not have genetic testing or testing limited to BRCA1/2. Participants received clinical genomic sequencing via a custom 60 gene panel. This study measured the feasibility of the Traceback methodology in OC survivors.
RESULTS RESULTS
The initial cohort included 929 individuals, of which 57% had no prior genetic testing. Of the 302 eligible for recruitment, 88 consented to participate. We were able to outreach 97% of the eligible population using contact information from medical records. The stage at diagnosis was the only factor associated with consent. Of the 78 who returned their saliva sample, 21% had pathogenic/likely pathogenic variants, and 79% had negative results.
CONCLUSION CONCLUSIONS
The GRACE study resulted in a 29% uptake of genetic testing in OC survivors. The time since diagnosis did not have an impact on consent or ability to contact. GRACE can inform the implementation of future Traceback programs, providing guidance on how to prevent and mitigate the burden of OC and other hereditary cancers.

Identifiants

pubmed: 39061202
pii: cancers16142563
doi: 10.3390/cancers16142563
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : NIH HHS
ID : 1U01CA244323-00X1
Pays : United States

Auteurs

Larissa L White (LL)

Institute for Health Research, Kaiser Permanente Colorado, 16601 East Centretech Parkway, Aurora, CO 80011, USA.

Jennifer K Sawyer (JK)

Institute for Health Research, Kaiser Permanente Colorado, 16601 East Centretech Parkway, Aurora, CO 80011, USA.

Jamilyn M Zepp (JM)

Center for Health Research, Department of Translational and Applied Genomics, Kaiser Permanente Northwest, 3800 North Interstate Avenue, Portland, OR 97227, USA.

Yolanda K Prado (YK)

Center for Health Research, Department of Translational and Applied Genomics, Kaiser Permanente Northwest, 3800 North Interstate Avenue, Portland, OR 97227, USA.

Ana A Reyes (AA)

Center for Health Research, Department of Translational and Applied Genomics, Kaiser Permanente Northwest, 3800 North Interstate Avenue, Portland, OR 97227, USA.

Mahesh Maiyani (M)

Institute for Health Research, Kaiser Permanente Colorado, 16601 East Centretech Parkway, Aurora, CO 80011, USA.

Elizabeth Shuster (E)

Center for Health Research, Department of Translational and Applied Genomics, Kaiser Permanente Northwest, 3800 North Interstate Avenue, Portland, OR 97227, USA.

Rachel Zucker (R)

Institute for Health Research, Kaiser Permanente Colorado, 16601 East Centretech Parkway, Aurora, CO 80011, USA.

Nora B Henrikson (NB)

Kaiser Permanente Washington Health Research Institute, 1730 Minor Avenue, Seattle, WA 98101, USA.

Alan F Rope (AF)

Center for Health Research, Department of Translational and Applied Genomics, Kaiser Permanente Northwest, 3800 North Interstate Avenue, Portland, OR 97227, USA.
Genome Medical, 701 Gateway Boulevard, South San Francisco, CA 94080, USA.

Sheila Weinmann (S)

Center for Health Research, Department of Translational and Applied Genomics, Kaiser Permanente Northwest, 3800 North Interstate Avenue, Portland, OR 97227, USA.

Heather S Feigelson (HS)

Institute for Health Research, Kaiser Permanente Colorado, 16601 East Centretech Parkway, Aurora, CO 80011, USA.

Jessica Ezzell Hunter (J)

Center for Health Research, Department of Translational and Applied Genomics, Kaiser Permanente Northwest, 3800 North Interstate Avenue, Portland, OR 97227, USA.
Genomics, Ethics, and Translational Research Program, RTI International, 3040 East Cornwallis Road, Research Triangle Park, NC 27709, USA.

Classifications MeSH