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French Childhood Cancer Survivor Study For Leukaemia (LEA Cohort)
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Sample details

The LEA cohort is a dynamic, open cohort studying the determinants of medium and long-term outcomes of patients treated for paediatric leukaemia. The study recruited participants who had a diagnosis of acute leukaemia when they were under 18 years old. Potential participants also needed to be living in France and have received their diagnosis after January of 1980, amongst other inclusion criteria. The study began in 2004 with recruitment from University hospitals in Marseille and Nancy and expanded to include Nice, Clermont-Ferrand, Grenoble, Lyon, Paris-Saint Louis, Paris-Trousseau, Paris-Robert Debré and Saint-Etienne by 2011. As of 2011, over 1,500 cancer survivors have agreed to take part in the study.

Study design
Cohort - clinical

Number of participants at first data collection

1,545 (participants)

Age at first data collection

Varied (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Cancer patients
Pediatric cancer patients
Dataset details

Country

France

Year of first data collection

2004

Primary Institutions

Aix-Marseille University (AMU)

Links

plateforme-lea.fr/en/les-projets-realises-et-en-cours/

Profile paper DOI

doi.org/10.1093/ije/dyu031

Funders

Canceropôle Provence-Alpes-Côte d’Azur (PACA)

French Institute for Public Health Research (Institut français de recherche en santé publique, IReSP)

French National Cancer Institute (Institut National du Cancer, INCA)

French National Research Agency (ANR)

Regional Council PACA

Ongoing?
Yes

Data types collected

mentalHealthData
dataLinkage
Quantitative data collection
  • Computer, paper or task testing (e.g. cognitive testing, theory of mind doll task, attention computer tasks)
  • Interview – face-to-face
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
  • Self-report questionnaire – unspecified
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
Features

Engagement

  • None
  • Keywords

    Biological samples/biospecimens
    Childhood cancer
    Clinical cohort
    Health and wellbeing
    Leukaemia
    Quality of life
    Remission
    Sociodemographics
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