REal World Data in LYmphoma and Survival in Adults

  • End date
    Oct 22, 2027
  • participants needed
  • sponsor
    Hospices Civils de Lyon
Updated on 22 January 2021


REALYSA cohort is a population-based epidemiological platform in real-life for lymphomas designed to enrich prognostic data, by integrating together epidemiological, clinical and biological data.

REALYSA is a platform perfectly set up to

  • Study prognostic factors using integrated epidemiological and biological data (genetics), to better characterize the determinants of refractoriness and relapse in patients with lymphoma, to follow the growing number of survivors and describe median to long-term sequela, second cancer, quality of life (QoL)
  • Document treatment effectiveness in real life and observance
  • Address socio-economical questions

Condition Follicular Lymphoma, Hodgkin's Disease, Lymphoma, MALT Lymphoma, Mantle cell lymphoma, Lymphoma, T-Cell Lymphoma, Non-Hodgkin's Lymphoma, Marginal Zone Lymphoma, hodgkin, hodgkin's lymphomas, hodgkin lymphomas, hodgkins lymphoma, hodgkin's lymphoma, t cell lymphoma, Diffuse Large B Lymphoma (DLBCL), Burkitt Lymphoma (BL))
Treatment Real-life epidemiological platform of lymphoma in France
Clinical Study IdentifierNCT03869619
SponsorHospices Civils de Lyon
Last Modified on22 January 2021


Yes No Not Sure

Inclusion Criteria

Is your age greater than or equal to 18 yrs?
Gender: Male or Female
Do you have any of these conditions: hodgkin's lymphomas or Marginal Zone Lymphoma or MALT Lymphoma or hodgkin lymphomas or hodgkin's lymphoma or t cell lymphoma or Hodgkin's Disease or B...?
Signature of the consent form for participation in the REALYSA cohort
Aged over 18 at the time of inclusion
Diagnosed with lymphoma in the last 6 months (180 days)
Lymphoma subtype belonging to at least one of the 7 histological subtypes: diffuse large B-cell lymphoma, follicular lymphoma, mantle cell lymphoma, marginal zone lymphoma, T-cell lymphoma, Hodgkin's lymphoma, Burkitt lymphoma

Exclusion Criteria

Anti-lymphoma treatment already received (except pre-phase: typically corticosteroids, vincristine, cyclophosphamide, etoposide, alone or in combination)
Documented HIV infection
Any other lymphoma subtype not included in the list in Appendix 1. Of note, are
Chronic lymphocytic leukemia/small lymphocytic lymphoma
Hairy cell leukemia and variant
Lymphoplasmacytic lymphoma
Waldenstrm macroglobulinemia
Primary DLBCL of the central nervous system (CNS)
T-cell large granular lymphocytic leukemia
Chronic lymphoproliferative disorder of NK cells
Mycosis fungoides
Szary syndrome
Primary cutaneous T cell lymphomas (mainly diagnosed and treated by dermatologists)
Post-transplant lymphoproliferative disorders (PTLD)
Clear my responses

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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