Evidence map›Paper›PMID 41733729›Full record

ReviewFamilial cancer2026

From theory to practice: improving Lynch syndrome recognition through evidence-based education.

Silvia Sanduleanu-Dascalescu, Gabriel Dimofte, Han-Mo Chiu, Bogdan Cotruta, Stefan Morarasu, Hans Vasen

Abstract readReview
PubMed Publisher
In one paragraph

Review in Familial cancer, 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.

Silvia Sanduleanu-DascalescuDepartment of Gastroenterology and Hepatology, Maastricht UMC+, Maastricht, The Netherlands. s.sanduleanu@gmail.com.
Gabriel DimofteGrigore T. Popa University of Medicine and Pharmacy Iasi, Regional Institute of Oncology Iasi, Iasi, Romania.
Han-Mo ChiuDepartment of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Bogdan CotrutaDepartment of Gastroenterology and Hepatology, Fundeni Clinical Institute, Bucharest, Romania.
Stefan MorarasuGrigore T. Popa University of Medicine and Pharmacy Iasi, Regional Institute of Oncology Iasi, Iasi, Romania.
Hans VasenDepartment of Gastroenterology and Hepatology, Leiden UMC, Leiden, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although genomic medicine has improved understanding of Lynch Syndrome (LS), many challenges remain in translating the knowledge in clinical practice. Between 1 in 279 and 400 persons in general population carry a pathogenic mutation in mismatch repair (MMR) genes linked to LS, but the vast majority remain undiagnosed. The clinical implementation gap arises from an interplay between physician factors, patient factors and logistic factors. In the first place, there is limited awareness and limited compliance among practicing physicians who often don’t recognize LS and don’t follow surveillance recommendations, missing opportunities to prevent cancer in affected persons and family members. One of the central problems lies in the current educational approach, particularly the lack of a curriculum on hereditary cancer syndromes during GI fellowship. Theoretical guidance alone is not actionable—it needs to be backed up by case-based practice with adequate provision both in terms of quantity and of insights. An evidence-based curriculum for achieving mastery standards on LS recognition and management shows early promise in fostering clinical transformation. Using repeat cycles of self-study and case-based practice with real-time feedback, learners can acquire base knowledge and problem-solving clinical decision skills faster and more effectively. This approach leads to a shift in practice. In the context of population screening programs for colorectal cancer (CRC) and gynecological cancers, this strategy can enhance the effectiveness of screening by reducing cancer incidence and mortality. Herein, we propose steps for the integration of LS screening into routine clinical practice, with particular focus on education.

Indexed as

Colorectal Neoplasms, Hereditary NonpolyposisCurriculumDNA Mismatch RepairEarly Detection of CancerEvidence-Based MedicineGenetic TestingHumansColorectal cancerEducationLynch syndromeScreening, hereditary colorectal cancer syndromeTraining

Identifiers

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.