Evidence map›Paper›PMID 34565430›Full record

ArticleHereditary cancer in clinical practice2021

Improving our model of cascade testing for hereditary cancer risk by leveraging patient peer support: a concept report.

Suzanne C O'Neill, Jada G Hamilton, Claire C Conley, Beth N Peshkin, Rosalba Sacca, Glynnis A McDonnell, Claudine Isaacs, Mark E Robson, Kenneth P Tercyak

Open access · goldAbstract read
In one paragraph

Article in Hereditary cancer in clinical practice, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 15 citations in OpenAlex.

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  11. Preparing for the unexpected: Recommendations for returning secondary findings in late-stage cancer care.Genetics in medicine : official journal of the American College of Medical Genetics · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Suzanne C O'NeillGeorgetown Lombardi Comprehensive Cancer Center, Washington, D.C, USA. sco4@georgetown.edu.
Jada G HamiltonMemorial Sloan Kettering Cancer Center, New York, USA.
Claire C ConleyGeorgetown Lombardi Comprehensive Cancer Center, Washington, D.C, USA.
Beth N PeshkinGeorgetown Lombardi Comprehensive Cancer Center, Washington, D.C, USA.
Rosalba SaccaMemorial Sloan Kettering Cancer Center, New York, USA.
Glynnis A McDonnellGeorgetown Lombardi Comprehensive Cancer Center, Washington, D.C, USA.
Claudine IsaacsGeorgetown Lombardi Comprehensive Cancer Center, Washington, D.C, USA.
Mark E RobsonMemorial Sloan Kettering Cancer Center, New York, USA.
Kenneth P TercyakGeorgetown Lombardi Comprehensive Cancer Center, Washington, D.C, USA.
Georgetown Lombardi Comprehensive Cancer CenterMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Tissue Culture Shared ResourceP30CA051008 · NCI · GEORGETOWN UNIVERSITY · PI Louis M Weiner · 1990 to 2026
$71.5M
Improving Genetic Counseling for BRCA+ MothersR01CA246589 · NCI · GEORGETOWN UNIVERSITY · PI PESHKIN, BETH N, TERCYAK, KENNETH · 2020 to 2024
$2.0M
Peer Support for Young Adult Women with High Breast Cancer RiskR01CA242750 · NCI · GEORGETOWN UNIVERSITY · PI O'NEILL, SUZANNE C., TERCYAK, KENNETH · 2020 to 2024
$1.8M
American Cancer Society MRSG-16-020-01-CPPBNCI NIH HHS P30 CA008748NCI NIH HHS P30 CA051008NCI NIH HHS P30CA051008NCI NIH HHS R01 CA242750NCI NIH HHS R01CA242750NCI NIH HHS R01 CA246589NCI NIH HHS R01CA246589
6 · The paper itself

Abstract

Consensus and evidence suggest that cascade testing is critical to achieve the promise of cancer genetic testing. However, barriers to cascade testing include effective family communication of genetic risk information and family members' ability to cope with genetic risk. These barriers are further complicated by the developmental needs of unaffected family members during critical windows for family communication and adaptation. Peer support could address these barriers. We provide two illustrative examples of ongoing BRCA1/2-related clinical trials that apply a peer support model to improve family communication and functioning. Peer support can augment currently available genetic services to facilitate adjustment to and effective use of cancer genetic risk information. Importantly, this scalable approach can address the presence of cancer risk within families across multiple developmental stages. This applies a family-centered perspective that accommodates all potentially at-risk relatives. This peer support model can be further applied to emerging topics in clinical genetics to expand reach and impact.

Indexed as

Cascade testingFamily communicationInterventionPeer coaching

Identifiers

PMID34565430
PMCPMC8474818
OpenAlexW3204709928

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.