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Molecular Prognosis of Lymphomas of the Central Nervous System (ALYCE-molecular)

Molecular Prognosis of Lymphomas of the Central Nervous System (ALYCE-molecular)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03859544
Acronym
ALYCEmolecular
Enrollment
74
Registered
2019-03-01
Start date
2016-01-01
Completion date
2020-01-01
Last updated
2019-03-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Central Nervous System Lymphoma

Brief summary

Central nervous system lymphoma (PCNSL) is a diffuse large B cell lymphoma (DLBCL) entity with a particularly poor prognosis (median survival less than 3 years). They are still poorly characterized biologically, largely because of their rarity (300 cases / year in France) and the difficulty for obtaining a material of sufficient quality and quantity. It is nevertheless assumed that their pathophysiology is particular, since they develop exclusively in an immunological sanctuary, and that they present some characteristic molecular abnormalities (mutation of MYD88 or TBL1XR1 for example). A collection of 74 PCNSLs has created, clinically annotated, from which frozen material is available in addition to the material fixed and included in paraffin (cohort ALYCE). Informed consent was gathered for all patients. Comparative Genomic Hybridization-array analysis of this cohort has already revealed abnormalities associated with a poor prognosis (unpublished data). The objective of this study is to complete this analysis by sequencing a panel of 96 mutant genes recurrently in DLBCLs and PCNSLs, and the molecular determination of the original cell by the (RT-MLPA) Reverse Transcriptase-Multiplex Ligation-dependent Probe Amplification technique. The integration of genetic, molecular and transcriptomic data may define prognostic markers and open perspectives for translational research in PCNSL.

Interventions

Retrospective study to search mutations associated with Central nervous system lymphoma and study of the prognostic impact (overall survival and progression-free survival) of these mutations.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Adults * With a lymphoma of the central nervous system * Patients having signed the consent for the conservation of their samples within the cohort

Exclusion criteria

* \<18 old years * Other diagnosis than lymphoma of the central nervous system * No consent form signed

Design outcomes

Primary

MeasureTime frameDescription
Progression free survivalUp to 48 monthsAnalysis of progression-free survival correlated with genomic data and mutation data

Countries

France

Contacts

Primary ContactHervé GHESQUIERES, Pr
herve.ghesquieres@chu-lyon.fr
Backup ContactPierre SUJOBERT, Dr
pierre.sujobert@chu-lyon.fr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026