Clinical outcomes and cumulative cost of preventive surveillance versus treatment in Li–Fraumeni syndrome: Results from the European PREVENTABLE project.

M Marion Rolain (Inserm U1245, Cancer And Brain Genomics, Rouen, France) J Jean Christophe Thery (Université de Rouen Normandie, Inserm U1245, FHU G4 Genomics, CHU Rouen, Département de Génétique, Rouen, France) R Ricardo Amorim (i3S – Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal) A Adriana Costal (Hereditary Cancer Program, Catalan Institute of Oncology - ICO, Girona, Spain) L Laura Duran-Lozano (Hereditary Cancer Genetics, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain) B Barbara Peleteiro (EPIUnit - Instituto de Saúde Pública da Universidade do Porto, Porto, Portugal) J Janneke Schuurs-Hoeijmakers (Radboudumc Department of Human Genetics, Nijmegen, Netherlands) M Marbelia Fernandes (i3S – Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal) L Liliana Sousa (i3S – Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal) S Sara Pereira H Hildegunn Høberg-Vetti (Haukeland University Hospital, Bergen, Norway) S Stefan Aretz (University of Bonn, University Hospital Bonn, National Centre for Hereditary Tumour Syndromes, Bonn, Germany) J Judith Balmana (Hereditary Cancer Genetics, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain) S Svetlana Bajalica-Lagercrantz J Joan Brunet P Preventable Consortium (i3S – Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal) C Carla Oliveira C Claude Houdayer

Abstract

10553 Background: Li-Fraumeni syndrome (LFS), caused by TP53 pathogenic variants, is one of the most severe hereditary cancer predisposition syndromes, characterized by very early cancer onset, broad tumor spectrum, and a high lifetime risk of multiple cancers. At the European level, no large-scale health economics study has compared LFS proactive cancer preventive management including intensive multiorgan surveillance and early cancer detection, with treatment approaches initiated after the first tumor occurs in individuals at high cancer risk. To address this gap, and within the European PREVENTABLE project, we evaluated healthcare pathways and cumulative costs of proactive prevention versus treatment in LFS European families. Methods: We retrospectively collected clinical data from 866 individuals from seven European countries (ERN GENTURIS centers), including 505 TP53 gene carriers (27% of whom were children) and 361 non-carrier family members. Based on multidisciplinary expertise, we developed a structured LFS care matrix, mapping patient clinical trajectories and clinical procedures across diagnosis, risk reduction strategies, surveillance and treatments. Costs were estimated using standardized French hospital tariffs, and data were collected via a GDPR-compliant digital tool interface developed by the PREVENTABLE consortium. Results: From 866 individuals, 155 were TP53 carriers without a prior cancer diagnosis at the time of genetic testing, defining the preventive arm. During follow-up (median 75 months; range 6–267), 20 individuals developed one or more cancers.The mean prevention cost per patient was €6,046.8 (range €451–€71,854.76). Among the 273 patients with a history of cancer prior to genetic testing, 109 had early-stage disease and 164 had advanced-stage disease (median follow-up 83 months; range 2–468). The mean treatment cost per patient was €53,906 (range €385.50–€440,760.93). Overall cumulative costs were €937,258 for prevention and €15,103,188 for treatment, including €5,245,915 for early-stage cancers and €9,857,273 for advanced-stage cancers. Preventive mastectomy was performed in 24% of women in either prevention or treatment groups. Conclusions: This first European cumulative cost analysis demonstrates that treatment costs for LFS far exceed prevention costs (9-fold), providing strong economic evidence in favor of early genetic diagnosis and preventive surveillance. These findings support public health decision-making and the harmonization of care pathways within the framework of precision medicine in Europe. Preventable is funded by the European Union (EU) under Grant nº 101095483.

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
Pages 10553-10553
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (18)

M

Marion Rolain

Inserm U1245, Cancer And Brain Genomics, Rouen, France

J

Jean Christophe Thery

Université de Rouen Normandie, Inserm U1245, FHU G4 Genomics, CHU Rouen, Département de Génétique, Rouen, France

R

Ricardo Amorim

i3S – Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal

A

Adriana Costal

Hereditary Cancer Program, Catalan Institute of Oncology - ICO, Girona, Spain

L

Laura Duran-Lozano

Hereditary Cancer Genetics, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain

B

Barbara Peleteiro

EPIUnit - Instituto de Saúde Pública da Universidade do Porto, Porto, Portugal

J

Janneke Schuurs-Hoeijmakers

Radboudumc Department of Human Genetics, Nijmegen, Netherlands

M

Marbelia Fernandes

i3S – Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal

L

Liliana Sousa

i3S – Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal

S

Sara Pereira

H

Hildegunn Høberg-Vetti

Haukeland University Hospital, Bergen, Norway

S

Stefan Aretz

University of Bonn, University Hospital Bonn, National Centre for Hereditary Tumour Syndromes, Bonn, Germany

J

Judith Balmana

Hereditary Cancer Genetics, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain

S

Svetlana Bajalica-Lagercrantz

J

Joan Brunet

P

Preventable Consortium

i3S – Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal

C

Carla Oliveira

C

Claude Houdayer