The LEGACy study: a European and Latin American consortium to identify risk factors and molecular phenotypes in gastric cancer to improve prevention strategies and personalized clinical decision making globally
Tessa Suzanne van Schooten,
Sarah Derks,
Elena Jiménez-Martí,
Fatima Carneiro,
Ceu Figueiredo,
Erika Ruiz,
Maria Alsina,
Cristina Molero,
Marcelo Garrido,
Arnoldo Riquelme,
Carmelo Caballero,
Eva Lezcano,
Juan Manuel O’Connor,
Federico Esteso,
Judith Farrés,
José Manuel Mas,
Florian Lordick,
Jeannette Vogt,
Antonella Cardone,
Charis Girvalaki,
Andrés Cervantes,
Tania Fleitas,
on behalf of the members of LEGACy consortium
Affiliations
Tessa Suzanne van Schooten
Amsterdam UMC-location VUMC, Department of Medical Oncology, Cancer Center Amsterdam
Sarah Derks
Amsterdam UMC-location VUMC, Department of Medical Oncology, Cancer Center Amsterdam
Elena Jiménez-Martí
Instituto Investigación Sanitaria INCLIVA (INCLIVA), CIBERONC, Medical Oncology Department, Hospital Clínico Universitario de Valencia, Universitat de Valencia
Fatima Carneiro
Institute of Pathology and Molecular Immunology of the University of Porto (IPATIMUP)/Institute of Research and Innovation in Health (i3S); Faculty of Medicine, University of Porto
Ceu Figueiredo
Institute of Pathology and Molecular Immunology of the University of Porto (IPATIMUP)/Institute of Research and Innovation in Health (i3S); Faculty of Medicine, University of Porto
Erika Ruiz
Instituto Nacional de Cancerología (INCAN), Translational Medicine Laboratory & GI Cancer Department
Maria Alsina
Valld’Hebron Institute of Oncology (VHIO), Medical Oncology Department
Cristina Molero
Valld’Hebron Institute of Oncology (VHIO), Medical Oncology Department
Marcelo Garrido
Pontificia Universidad Católica de Chile (PUC), Department of Hemato-Oncology
Arnoldo Riquelme
Pontificia Universidad Católica de Chile (PUC), Department of Hemato-Oncology
Carmelo Caballero
GenPat
Eva Lezcano
Instituto de Previsión Social
Juan Manuel O’Connor
Instituto Alexander Fleming (IAF), Medical Oncology Department
Federico Esteso
Instituto Alexander Fleming (IAF), Medical Oncology Department
Judith Farrés
Anaxomics Biotech, S.L. (ANAX)
José Manuel Mas
Anaxomics Biotech, S.L. (ANAX)
Florian Lordick
Universitaet Leipzig (ULEI), Medical Oncology Department
Jeannette Vogt
Universitaet Leipzig (ULEI), Medical Oncology Department
Antonella Cardone
European Cancer Patient Coalition (ECPC)
Charis Girvalaki
European Cancer Patient Coalition (ECPC)
Andrés Cervantes
Instituto Investigación Sanitaria INCLIVA (INCLIVA), CIBERONC, Medical Oncology Department, Hospital Clínico Universitario de Valencia, Universitat de Valencia
Tania Fleitas
Instituto Investigación Sanitaria INCLIVA (INCLIVA), CIBERONC, Medical Oncology Department, Hospital Clínico Universitario de Valencia, Universitat de Valencia
Abstract Background Gastric Cancer (GC) is the fourth most deadly cancer worldwide. Enhanced understanding of its key epidemiological and molecular drivers is urgently needed to lower the incidence and improve outcomes. Furthermore, tumor biology in European (EU) and Latin American (LATAM) countries is understudied. The LEGACy study is a Horizon 2020 funded multi-institutional research approach to 1) detail the epidemiological features including risk factors of GC in current time and 2) develop cost-effective methods to identify and integrate biological biomarkers needed to guide diagnostic and therapeutic approaches with the aim of filling the knowledge gap on GC in these areas. Methods This observational study has three parts that are conducted in parallel during 2019–2023 across recruiting centers from four EU and four LATAM countries: Part 1) A case-control study (800 cases and 800 controls) using questionnaires on candidate risk factors for GC, which will be correlated with clinical, demographic and epidemiological parameters. Part 2) A case-control tissue sampling study (400 cases and 400 controls) using proteome, genome, microbiome and immune analyses to characterize advanced (stage III and IV) GC. Patients in this part of the study will be followed over time to observe clinical outcomes. The first half of samples will be used as training cohort to identify the most relevant risk factors and biomarkers, which will be selected to propose cost-effective diagnostic and predictive methods that will be validated with the second half of samples. Part 3) An educational study, as part of our prevention strategy (subjects recruited from the general public) to test and disseminate knowledge on GC risk factors and symptoms by a questionnaire and informative video. Patients could be recruited for more than one of the three LEGACy studies. Discussion The LEGACy study aims to generate novel, in-depth knowledge on the tumor biological characteristics through integrating epidemiological, multi-omics and clinical data from GC patients at an EU-LATAM partnership. During the study, cost-effective panels with potential use in clinical decision making will be developed and validated. Trial registration ClinicalTrials.gov Identifiers: Part 1: NCT03957031 . Part 2: NCT04015466 . Part 3: NCT04019808 .