Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers
Inserm · Institute for Research and Innovation in Biomedicine
Abstract
PURPOSE: The aim of the study was to update the description of Li-Fraumeni syndrome (LFS), a remarkable cancer predisposition characterized by extensive clinical heterogeneity. PATIENTS AND METHODS: From 1,730 French patients suggestive of LFS, we identified 415 mutation carriers in 214 families harboring 133 distinct TP53 alterations and updated their clinical presentation. RESULTS: The 322 affected carriers developed 552 tumors, and 43% had developed multiple malignancies. The mean age of first tumor onset was 24.9 years, 41% having developed a tumor by age 18. In childhood, the LFS tumor spectrum was characterized by osteosarcomas, adrenocortical carcinomas (ACC), CNS tumors, and soft tissue sarcomas (STS)…
Citation impact
- FWCI
- 20.63
- Percentile
- 100%
- References
- 42
Authors
18- GBGaëlle BougeardCorresponding
Inserm, Institute for Research and Innovation in Biomedicine
- MRMariette Renaux‐Petel
Inserm, Institute for Research and Innovation in Biomedicine
- JFJean‐Michel Flaman
Inserm, Institute for Research and Innovation in Biomedicine
- CCCamille Charbonnier
Inserm, Institute for Research and Innovation in Biomedicine
- PFPierre Fermey
Inserm, Institute for Research and Innovation in Biomedicine
Topics & keywords
- Li–Fraumeni syndrome
- Medicine
- Missense mutation
- Cancer
- Germline mutation
- Breast cancer
- Germline
- Internal medicine
- Good health and well-being