Evidence map›Paper›PMID 41670817›Full record

ReviewClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2026

Inherited cancer syndromes in adult oncology: a referral guide based on malignant tumor and polyp features.

Audrey Guilmot, Magali Belpaire, Eric Olinger, Anne De Leener, Kevin Punie, Francois P Duhoux

Abstract readReview
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In one paragraph

Review in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2026. 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
–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

0 citing papers in PubMed.

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

6 authors.

Audrey GuilmotCenter for Human Genetics, Cliniques universitaires Saint-Luc, Brussels, Belgium. audrey.guilmot@chuv.ch.ORCID http://orcid.org/0009-0005-6956-0772
Magali BelpaireCenter for Human Genetics, Cliniques universitaires Saint-Luc, Brussels, Belgium.
Eric OlingerCenter for Human Genetics, Cliniques universitaires Saint-Luc, Brussels, Belgium.
Anne De LeenerCenter for Human Genetics, Cliniques universitaires Saint-Luc, Brussels, Belgium.
Kevin PunieGZA Ziekenhuizen Campus Sint-Augustinus, Antwerp, Belgium.
Francois P DuhouxCenter for Human Genetics, Cliniques universitaires Saint-Luc, Brussels, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDue to the challenges of identifying patients with hereditary cancer predispositions in oncology practice, we propose a comprehensive and practical tool intended for oncologists managing adult patients with malignant solid tumors and/or gastrointestinal polyps.

methodsThis tool was developed based on a comprehensive review of international guidelines, GeneReviews, and recent literature. Key criteria for genetic referral were compiled and organized by organ site and tumor subtype.

resultsThe resulting resource includes a primary reference table for genetic referral, a polyposis-specific table, two visual summary figures and curated lists of associated genes and syndromes to streamline the clinical decision-making process.

conclusionsThis comprehensive tool aims to support oncologists in the timely identification of patients eligible for genetic counseling, thereby enhancing therapeutic decisions and improving familial risk assessment.

Indexed as

NeoplasmsNeoplastic Syndromes, HereditaryReferral and ConsultationAdultGenetic CounselingGenetic Predisposition to DiseaseHumansMedical OncologyPractice Guidelines as Topiccancer predispositiongenetic counselinghereditary cancer syndromepolyposis syndromes

Identifiers

What Socratic holds

Textmetadata
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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 Socratic graph.