Evidence map›Paper›PMID 35621678›Full record

ArticleCurrent oncology (Toronto, Ont.)2022

Patient Experience with a Gynecologic Oncology-Initiated Genetic Testing Model for Women with Tubo-Ovarian Cancer.

Michaela Bercovitch Sadinsky, Joanne Power, Enza Ambrosio, Laura Palma, Xing Zeng, William D Foulkes, Evan Weber

Open access · goldAbstract read
In one paragraph

Article in Current oncology (Toronto, Ont.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 2 institutions in 1 country.

Michaela Bercovitch SadinskyDepartment of Human Genetics, McGill University, Montreal, QC H3A0C7, Canada.ORCID 0000-0002-1592-9467
Joanne PowerDivision of Gynecologic Oncology, McGill University Health Centre, Montreal, QC H4A3J1, Canada.
Enza AmbrosioDivision of Gynecologic Oncology, McGill University Health Centre, Montreal, QC H4A3J1, Canada.
Laura PalmaDepartment of Human Genetics, McGill University, Montreal, QC H3A0C7, Canada.
Xing ZengDivision of Gynecologic Oncology, McGill University Health Centre, Montreal, QC H4A3J1, Canada.
William D FoulkesDepartment of Human Genetics, McGill University, Montreal, QC H3A0C7, Canada.
Evan WeberDepartment of Human Genetics, McGill University, Montreal, QC H3A0C7, Canada.
McGill University Health Centre · CAJewish General Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUp to 20% of women diagnosed with tubo-ovarian carcinoma carry a germline pathogenic variant in a cancer-predisposing gene (e.g.,

methodsStudy participants were patients diagnosed with high-grade non-mucinous epithelial tubo-ovarian cancer who underwent genetic testing through the GOIGT model between 1 January 2017 and 31 December 2020. Eligible participants completed the retrospective questionnaires at least one month after result disclosure.

resultsA total of 126 patients were tested through the GOIGT model during the study period, of which 56 were invited to participate. Thirty-four participants returned the study questionnaire. Overall, participants did not report decision regret following the genetic testing and were satisfied with the GOIGT model. Participants reported low levels of uncertainty and distress related to the implications of their test results for themselves and their family members.

conclusionsThe results of this study support the continued implementation of mainstreamed genetic testing models for women with high-grade non-mucinous tubo-ovarian cancer. Further studies are required to compare experiences for patients with different genetic test results.

Indexed as

Ovarian NeoplasmsFemaleGenes, BRCA2Genetic TestingHumansPatient Outcome AssessmentRetrospective Studiesgenetic counsellinggenetic testinghereditary cancermainstreamingpatient experience

Identifiers

PMID35621678
PMCPMC9139592
OpenAlexW4280560166

What OpenQuestion holds

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LicenceCC BY
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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.