Lymphoma, Large B-Cell, Diffuse Clinical Trial
Official title:
Identification Predictive Markers of Immunochemotherapy Response to the Primary Cutaneous Diffuse Large B Cell Lymphoma by Transcriptomic Proteomics and Mutational Analysis
The study is performed on a single-center retrospective cohort of 32 patients LBC-TJ treated with R-chemotherapy for which data collection was carried out in homogeneous and prospectively followed according to international standards through RCP monthly cutaneous lymphomas managed by Professor Beylot-Barry and inclusion of cases in the national database of rare cancer network French Study Group of Cutaneous Lymphomas in Bordeaux managed by Prof. Beatrice Vergier. Fourteen patients responded to the R-PCT against 18 non-responders, 14 patients for whom we have the sample to recidivism.
The objective is to identify predictive biomarkers of response to R-chemotherapy and
understand what genomic markers, transcriptomic or proteomic would identify those patients
ahead. This would ultimately help to identify whether dysregulated biological pathway could
be targeted specifically among patients with personalized treatment.
Like its counterpart systemic Lymphoma Diffuse large B cell, the sequential analysis of the
same patient at diagnosis and relapse can also identify candidate genes and biological
pathways involved in recurrence and help to design new therapeutic strategies.
Another objective is ultimately the development of an integrative bioinformatics tool for
anticipating the therapeutic response. The tumor model used is certainly a rare cancer but
prototypical ABC lymphomas allowing access to relapse hardware and relative homogeneity that
will allow a study of a smaller number of cases for the development of correlations models
genomics / proteomics. This is a pivotal project integrating proteomic data and Molecular
Biology (mutation, expression) based on the pooling of skills of clinical teams, biological
and bioinformatics to validate a predictive model for treatment response able to integrate
prognostic markers known as TNM the dual expression MYC / BCL2 and forward to predict the
therapeutic response using this modeling by CBIB. We would then validate the model
established in this series of training on a range of national validation as part of an
observational study with GFELC (Groupe Français d'Etude des Lymphomes Cutanés).
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