Evidence map›Paper›PMID 41772285›Full record

ArticleEuropean journal of human genetics : EJHG2026

Challenges in identifying paediatric cancer predisposition syndromes: international SCOPE survey and SIOPE expert consensus recommendations.

Jakica Ćavar Pavić, Noelle Cullinan, Marjolijn Jongmans, Franck Bourdeaut, Karin Wadt, Luca LoNigro, Mark Davies, Orli Michaeli, Sonja Strang-Karlsson, Robin de Putter and 6 more

Abstract readConsensus Statement
In one paragraph

Article in European journal of human genetics : EJHG, 2026. 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

16 authors.

Jakica Ćavar PavićDivision of Paediatric Haematology and Oncology, Department of Paediatrics, University Children's Hospital Inselspital, Bern, Switzerland.ORCID http://orcid.org/0009-0009-7573-6921
Noelle CullinanDepartment of Paediatric Haematology-Oncology, Children's Health Ireland, Dublin, Ireland.ORCID http://orcid.org/0000-0002-4840-5010
Marjolijn JongmansPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Franck BourdeautUniversité Paris Cité - INSERM U1330, Laboratory of Translational Research in Pediatric Oncology, SIREDO Paediatric Oncology Center, Institute Curie, Paris, France.ORCID http://orcid.org/0000-0001-9489-6781
Karin WadtDepartment of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
Luca LoNigroCenter of Paediatric Haematology-Oncology, Azienda Policlinico-San Marco, Catania, Italy.
Mark DaviesDepartment of Genetics and Oncology, Cardiff University, Cardiff, UK.
Orli MichaeliDepartment of Paediatric Haematology and Oncology, Schneider Children's Medical Center of Israel, Petah Tikva, Israel; Faculty of Medical & Health Sciences, Tel-Aviv University, Tel-Aviv, Israel.
Sonja Strang-KarlssonDepartment of Clinical Genetics, HUS Diagnostic Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Robin de PutterCenter for Medical Genetics, Ghent University Hospital, Ghent, Belgium.ORCID http://orcid.org/0000-0001-9410-8941
Edith SepulchreDepartment of Human Genetics, GIGA Research Center-University of Liège and Centre Hospitalier Universitaire Liège, Liège, Belgium.
Giovanni CazzanigaTettamanti Center, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
Rhoikos FurtwänglerDivision of Paediatric Haematology and Oncology, Department of Paediatrics, University Children's Hospital Inselspital, Bern, Switzerland.ORCID http://orcid.org/0000-0002-1967-8343
Christiane ZweierDepartment for Biomedical Research (DBMR), University of Bern, Bern, Switzerland.ORCID http://orcid.org/0000-0001-8002-2020
Jochen RösslerDivision of Paediatric Haematology and Oncology, Department of Paediatrics, University Children's Hospital Inselspital, Bern, Switzerland.
Nicolas WaespeDivision of Paediatric Haematology and Oncology, Department of Paediatrics, University Children's Hospital Inselspital, Bern, Switzerland. nicolas.waespe@unibe.ch.ORCID http://orcid.org/0000-0002-2271-8959

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer Predisposition Syndromes (CPS) are heritable genetic conditions associated with an increased risk of developing various cancers throughout life. While early identification and tumour surveillance can improve outcomes, CPS are often underdiagnosed in clinical practice. To evaluate clinicians' perspectives and identify barriers to CPS identification and care across Europe, we conducted the SCOPE study: a three-part cross-sectional survey of paediatric haematology/oncology professionals, followed by a modified Delphi consensus process with members of the SIOP Europe Host Genome Working Group. A total of 185 paediatric oncologists from 22 countries participated in the survey. More than 40% of participants reported low or uncertain confidence across different CPS-related tasks, particularly in counselling families (64.3%) and interpreting germline genetic findings (57.3%). Access to clinical geneticists and dedicated CPS clinics were predictors of higher confidence for some domains, while individual experience and institutional patient volume had limited influence. Regular use of universal CPS screening tools was low (42.3%), with most clinicians relying on personal judgement rather than structured criteria. The most cited barriers were lack of screening guidelines (57%) and difficulties in interpreting results (35.1%). Regular training and workshops, availability of genetic counsellors or educators for patient support, and patient-friendly education material were most cited as areas of improvement. The Delphi process led to three recommendations: (1) improve clinician training and communication strategies, (2) integrate CPS screening into standard treatment plans, and (3) develop accessible, patient-centred educational materials. These recommendations highlight opportunities to enhance CPS care through structured support, interdisciplinary collaboration, and systematic screening approaches.

Indexed as

Genetic Predisposition to DiseaseGenetic TestingNeoplasmsNeoplastic Syndromes, HereditaryChildCross-Sectional StudiesEuropeFemaleGenetic CounselingHumansMaleSurveys and Questionnaires

Identifiers

PMID41772285
PMCPMC13550621

What OpenQuestion holds

Textmetadata
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.