The impact of different treatment strategies on minimal residual disease (MRD) in young and elderly Mantle cell lymphoma (MCL) patients.

Anno
2017
Proponente Alice Di Rocco - Ricercatore
Sottosettore ERC del proponente del progetto
Componenti gruppo di ricerca
Componente Categoria
Alessandro Pulsoni Componenti il gruppo di ricerca
Luigi Petrucci Dottorando/Assegnista/Specializzando componente il gruppo di ricerca
Maurizio Martelli Componenti il gruppo di ricerca
Componente Qualifica Struttura Categoria
Irene Della Starza Biologo Biotecnologie cellulari ed Ematologia Altro personale Sapienza o esterni
Abstract

Despite the recent substantial improvement of clinical outcome in Mantle cell lymphoma (MCL), resistance to immunochemotherapy and common relapses are challenges for long-term tumor control.
The assessment of Minimal Residual Disease (MRD) by Real-Time Quantitative Polymerase Chain Reaction (RQ-PCR) has emerged as a widely feasible and standardized tool for direct assessment of therapy-induced reduction of tumor burden and regrowth after cytotoxic treatment in MCL, with much improved sensitivity compared with conventional staging procedures. Several studies have shown that intensification of initial treatment, which has resulted in improved clinical outcome, is immediately reflected in higher molecular remission rates; they have also shown that high-dose consolidation might not be able to compensate for less intensive induction regimens. Persistence or reappearance of MRD in clinical remission proved to be highly predictive for early clinical relapse associated with shorter overall survival. Therefore, the integration of MRD assessment into clinical response criteria could result in a more specific and potentially earlier end point for treatment efficacy. The aim of our project is to evaluate the MRD remission rate induced by different immunochemotherapy regimens in MCL patients, treated at our institution. MRD assessment will be performed in different time points: at baseline, during/after the treatment and during follow up for 24 months every 6 months.

ERC
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