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Open Access 11-01-2024 | Endoscopy

Li Fraumeni Syndrome predisposes to gastro-esophageal junction tumours

Authors: Douglas Tjandra, Alex Boussioutas

Published in: Familial Cancer | Issue 1/2024

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Abstract

Li-Fraumeni Syndrome (LFS), caused by germline pathogenic variants in TP53, predisposes to a wide range of young-onset malignancies, particularly sarcoma, breast and brain cancer. More recently, an increased risk of gastric adenocarcinoma has been recognised, although uptake of surveillance upper endoscopy is unclear. Our retrospective review of 65 patients with LFS, of whom 53.8% had undergone endoscopy, identified four patients (6.2%) with gastro-esophageal junction (GEJ) adenocarcinomas. Two cases were found on asymptomatic screening and were early stage. No cases had family history of gastrointestinal malignancy. Reviewing genomic data from The Cancer Genome Atlas Program, 76.4% of sporadic esophageal adenocarcinomas harboured somatic TP53 pathogenic variants, compared with 39.9% of non-cardia gastric cancers. This similar pattern observed in germline and sporadic cases warrants further investigation. We propose that upper endoscopy be recommended to all patients with LFS, with a focus on appropriate surveillance of the GEJ.
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Metadata
Title
Li Fraumeni Syndrome predisposes to gastro-esophageal junction tumours
Authors
Douglas Tjandra
Alex Boussioutas
Publication date
11-01-2024
Publisher
Springer Netherlands
Published in
Familial Cancer / Issue 1/2024
Print ISSN: 1389-9600
Electronic ISSN: 1573-7292
DOI
https://doi.org/10.1007/s10689-023-00353-0

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