Achieving universal genetic assessment for women with ovarian cancer: Are we there yet? A systematic review and meta-analysis.
BRCA1 Protein
/ genetics
BRCA2 Protein
/ genetics
DNA Mutational Analysis
/ statistics & numerical data
Early Detection of Cancer
/ statistics & numerical data
Female
Genetic Counseling
/ organization & administration
Genetic Testing
/ statistics & numerical data
Humans
Ovarian Neoplasms
/ diagnosis
Referral and Consultation
/ organization & administration
Telemedicine
/ organization & administration
Cascade testing
Genetic counseling
Genetic testing
Hereditary cancer syndromes
Ovarian cancer
Journal
Gynecologic oncology
ISSN: 1095-6859
Titre abrégé: Gynecol Oncol
Pays: United States
ID NLM: 0365304
Informations de publication
Date de publication:
08 2021
08 2021
Historique:
received:
10
03
2021
accepted:
08
05
2021
pubmed:
24
5
2021
medline:
15
12
2021
entrez:
23
5
2021
Statut:
ppublish
Résumé
Several professional organizations recommend universal genetic assessment for people with ovarian cancer as identifying pathogenic variants can affect treatment, prognosis, and all-cause mortality for patients and relatives. We sought to evaluate the literature on genetic assessment for women with ovarian cancer and determine if any interventions or patient characteristics drive utilization of services. We searched key electronic databases to identify trials that evaluated genetic assessment for people with ovarian cancer. Trials with the primary aim to evaluate utilization of genetic assessment with or without interventions were included. Eligible trials were subjected to meta-analysis and the moderating influence of health interventions on rates of genetic assessment were examined. A total of 35 studies were included (19 report on utilization of genetic services without an intervention, 7 with an intervention, and 9 with both scenarios). Without an intervention, pooled estimates for referral to genetic counseling and completion of genetic testing were 39% [CI 27-53%] and 30% [CI 19-44%]. Clinician-facilitated interventions included: mainstreaming of genetic services (99% [CI 86-100%]), telemedicine (75% [CI 43-93%]), clinic-embedded genetic counselor (76% [CI 32-95%]), reflex tumor somatic genetic assessment (64% [CI 17-94%]), universal testing (57% [28-82%]), and referral forms (26% [CI 10-53%]). Random-effects pooled proportions demonstrated that Black vs. White race was associated with a lower rate of genetic testing (26%[CI 17-38%] vs. 40% [CI 25-57%]) as was being un-insured vs. insured (23% [CI 18-28%] vs. 38% [CI 26-53%]). Reported rates of genetic testing for people with ovarian cancer remain well below the goal of universal testing. Interventions such as mainstreaming can improve testing uptake. Strategies aimed at improving utilization of genetic services should consider existing disparities in race and insurance status.
Identifiants
pubmed: 34023131
pii: S0090-8258(21)00407-8
doi: 10.1016/j.ygyno.2021.05.011
pmc: PMC8424684
mid: NIHMS1706684
pii:
doi:
Substances chimiques
BRCA1 Protein
0
BRCA1 protein, human
0
BRCA2 Protein
0
BRCA2 protein, human
0
Types de publication
Journal Article
Meta-Analysis
Research Support, N.I.H., Extramural
Systematic Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
506-516Subventions
Organisme : NCI NIH HHS
ID : R01 CA211723
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA233056
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : K07 CA216326
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002384
Pays : United States
Organisme : NCATS NIH HHS
ID : KL2 TR002385
Pays : United States
Informations de copyright
Copyright © 2021 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest Kevin Holcomb serves as a consultant for Johnson and Johnson and receives research support from Fujirebio Diagnostics, outside the submitted work. The other authors made no disclosures.
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