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Study of Families With an Hemopathies Predisposition Related to the DDX41 Gene.
Sponsor: Institut Claudius Regaud
Summary
This is a multicenter, interventional, historico-prospective cohort pilot study aimed at specifying the phenotype of subjects carrying a constitutional familial DDX41 mutation, with a view to eventually publishing oncogenetic recommendations for carriers of this mutation. The main objective of the LUCID project is to assess the cumulative risk of hematological diseases as a function of age in DDX41 germline mutation carriers. This study will be carried out in two stages: Stage 1: Inclusion of index cases in an oncogenetic consultation (salivary test, completion of an health self-questionnaire and collection of contact details for the related cases). Stage 2: Proposition of participation to family members, by correspondence, and determination of carrier or non-carrier status of the constitutional familial DDX41 mutation (based on a salivary test). A maximum of 210 index case patients and 700 family member will be included in this study.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
910
Start Date
2023-11-17
Completion Date
2030-01
Last Updated
2025-12-08
Healthy Volunteers
Yes
Conditions
Interventions
For each person (index case or related) included in this study:
* an health questionnaire will be completed in order to gather information on the participant's medical history and lifestyle. * a saliva sample will be taken (if applicable) so that a genetic analysis can be performed.
Locations (5)
Chu de Bordeaux
Bordeaux, France
Chu de Limoges
Limoges, France
Institut Paoli-Calmettes
Marseille, France
Chu de Montpellier
Montpellier, France
IUCT-O
Toulouse, France