Evidence map›Paper›PMID 40745491›Full record

Trial reportEuropean journal of human genetics : EJHG2025

Direct letters to relatives at risk of hereditary cancer-a randomised trial on healthcare-assisted versus family-mediated risk disclosure.

Hans Ehrencrona, Anna Öfverholm, Carolina Hawranek, Lovisa Lovmar, Sara Svensson, Sigrid Wennstedt, Barbro Hellquist, Anna Rosén

Abstract readMulticenter StudyPragmatic Clinical TrialRandomized Controlled Trial
In one paragraph

Trial report in European journal of human genetics : EJHG, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Quality of life, anxiety and cancer worry following hereditary cancer testing: a 6-month Swedish follow-up study.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2026
    Article
  4. Uncertainty, ethics, and progress in genomic medicine.European journal of human genetics : EJHG · 2025
    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

8 authors.

Hans EhrencronaDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.ORCID 0000-0002-5589-3622
Anna ÖfverholmDepartment of Oncology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Göteborg, Sweden.ORCID 0000-0002-1883-1924
Carolina HawranekDepartment of Diagnostics and Intervention, Oncology, Umeå University, Umeå, Sweden.ORCID 0000-0003-2218-6881
Lovisa LovmarDepartment of Clinical Genetics and Genomics, Sahlgrenska University Hospital, Gothenburg, Sweden.
Sara SvenssonDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Sigrid WennstedtDepartment of Medical Biosciences, Umeå University, Umeå, Sweden.
Barbro HellquistDepartment of Diagnostics and Intervention, Oncology, Umeå University, Umeå, Sweden.
Anna RosénDepartment of Diagnostics and Intervention, Oncology, Umeå University, Umeå, Sweden. anna.rosen@umu.se.ORCID 0000-0003-2441-2395

Funding

Cancerfonden (Swedish Cancer Society) 2020-1107Cancer Research Foundation in Northern Sweden (Northern Sweden Cancer Foundation) NAForskningsrådet om Hälsa, Arbetsliv och Välfärd (Swedish Research Council for Health, Working Life and Welfare) 2018-00964Vetenskapsrådet (Swedish Research Council) 2022-02226
6 · The paper itself

Abstract

Observational studies suggest that direct contact from healthcare to at-risk relatives may increase genetic counselling (GC) uptake as compared to family-mediated risk disclosure, but randomised controlled trials (RCTs) are lacking. This study assessed whether the offer of direct letters to relatives at risk of hereditary breast and ovarian cancer (HBOC) or Lynch syndrome increases GC uptake compared to family-mediated communication alone. Between 2020 and 2023, probands were randomly assigned to family-mediated disclosure (control) or family-mediated disclosure plus the offer of sending direct letters to at-risk relatives (intervention). The primary outcome was GC uptake within 12 months, measured as the proportion of eligible relatives at risk contacting a Swedish cancer genetics clinic. In total, 165 families (median: 4 eligible relatives, range: 1-26) were randomised to control (n = 79) or intervention (n = 86). GC uptake was 67% in controls and 71% in the intervention group (P = 0.23). After adjusting for predefined variables and covariates, there was still no significant difference between groups (OR: 1.24, CI: 0.79-1.95, P = 0.34). Distant relatives had lower uptake than first-degree relatives (OR: 0.27, CI: 0.18-0.40, P < 0.001), while female relatives had higher uptake than males (OR: 2.17, CI: 1.50-3.12, P < 0.001). This is the largest RCT so far investigating direct letters to relatives. GC uptake was high in both groups, and the intervention of direct letters did not show superiority over family-mediated communication alone. Direct letters to relatives may complement family-mediated disclosure in certain situations, but should not be implemented as a general procedure in cancer genetics practices.

Indexed as

Colorectal Neoplasms, Hereditary NonpolyposisCorrespondence as TopicDisclosureFamilyGenetic CounselingGenetic Predisposition to DiseaseHereditary Breast and Ovarian Cancer SyndromeAdultAgedFemaleHumansMaleMiddle Aged

Identifiers

PMID40745491
PMCPMC12480553

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.