Evidence map›Paper›PMID 37365297›Full record

ArticleHuman genetics2023

Regulating cancer risk prediction: legal considerations and stakeholder perspectives on the Canadian context.

Palmira Granados Moreno, Terese Knoppers, Ma'n H Zawati, Michael Lang, Bartha M Knoppers, Michael Wolfson, Hermann Nabi, Michel Dorval, Jacques Simard, Yann Joly

Abstract read
In one paragraph

Article in Human genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Palmira Granados MorenoCentre of Genomics and Policy, Faculty of Medicine, McGill University, Montréal, Québec, Canada.
Terese KnoppersCentre of Genomics and Policy, Faculty of Medicine, McGill University, Montréal, Québec, Canada. terese.knoppers@mcgill.ca.ORCID http://orcid.org/0000-0001-8912-1906
Ma'n H ZawatiCentre of Genomics and Policy, Faculty of Medicine, McGill University, Montréal, Québec, Canada.
Michael LangCentre of Genomics and Policy, Faculty of Medicine, McGill University, Montréal, Québec, Canada.
Bartha M KnoppersCentre of Genomics and Policy, Faculty of Medicine, McGill University, Montréal, Québec, Canada.
Michael WolfsonSchool of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.
Hermann NabiOncology Division, CHU de Québec-Université Laval Research Center, Québec City, Québec, Canada.
Michel DorvalOncology Division, CHU de Québec-Université Laval Research Center, Québec City, Québec, Canada.
Jacques SimardGenomics Center, CHU de Québec-Université Laval Research Center, Québec City, Québec, Canada.
Yann JolyCentre of Genomics and Policy, Faculty of Medicine, McGill University, Montréal, Québec, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Risk prediction models hold great promise to reduce the impact of cancer in society through advanced warning of risk and improved preventative modalities. These models are evolving and becoming more complex, increasingly integrating genetic screening data and polygenic risk scores as well as calculating risk for multiple types of a disease. However, unclear regulatory compliance requirements applicable to these models raise significant legal uncertainty and new questions about the regulation of medical devices. This paper aims to address these novel regulatory questions by presenting an initial assessment of the legal status likely applicable to risk prediction models in Canada, using the CanRisk tool for breast and ovarian cancer as an exemplar. Legal analysis is supplemented with qualitative perspectives from expert stakeholders regarding the accessibility and compliance challenges of the Canadian regulatory framework. While the paper focuses on the Canadian context, it also refers to European and U.S. regulations in this domain to contrast them. Legal analysis and stakeholder perspectives highlight the need to clarify and update the Canadian regulatory framework for Software as a Medical Device as it applies to risk prediction models. Findings demonstrate how normative guidance perceived as convoluted, contradictory or overly burdensome can discourage innovation, compliance, and ultimately, implementation. This contribution aims to initiate discussion about a more optimal legal framework for risk prediction models as they continue to evolve and are increasingly integrated into landscape for public health.

Indexed as

Ovarian NeoplasmsSoftwareCanadaFemaleGenetic TestingHumansRisk

Identifiers

PMID37365297
PMCPMC10329579

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.