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NCT04300101Recruiting

Mixed Molecular Clinical Index (MMCI) in Diffuse Large B-cell Lymphoma (DLBCL)

Source: ClinicalTrials.gov · Last updated 10 Apr 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is a prospective and retrospective observational study. The primary objective is to identify new prognostic biomarkers for DLBCL patients in terms of progression-free survival (PFS) and able to add predictive capacity to recognized important clinical factors. The secondary objectives are: * to identify new biomarkers associated with overall survival (OS) and objective response rate (ORR) * to characterize tissue and circulating immune microenvironment of DLBCL patients by bulk and single cell transcriptomics; * to assess the correlation between the expression of immune checkpoint genes and mRNA signature; * to describe the mutational status of a panel of genes relevant to DLBCL pathogenesis;. * to assess the correlation between protein expression, mutational status and the messenger RNA (mRNA) signature. * to investigate the association between radiomic features obtained from PET images and patient and tumour characteristics and clinical outcomes (PFS, OS, ORR). For each enrolled patient, immunohistochemical determinations will be performed: Cell of origin (COO) (Germinal Cell -GC- or activated B-cell - ABC- type according with Hans algorithm ), evaluation of cluster of differentiation antigen 20 (CD20), cluster of differentiation antigen 5 (CD5), cluster of differentiation antigen 10 (CD10), Bcl6, Bcl2 (cut off\>50%), Multiple Myeloma 1 / Interferon Regulatory Factor 4 protein (MUM1/IRF4), c-myc (cut off\>40%) and Ki67, fluorescence in situ hybridization (FISH) for c-myc and if rearranged, for Bcl2 e Bcl6 ). Moreover, paraffin embedded (FFPE) tumor specimens will be collected for RNA extraction and mRNA expression mutational and proteomics analysis, centralized at IRST-IRCCS.

Status (registry)
Recruiting
Study type
Observational
Enrollment
300 (estimated)
First submitted
5 Mar 2020
Start date
14 May 2020
Primary completion date
May 2026
Lead sponsor
Istituto Romagnolo per lo Studio dei Tumori Dino Amadori IRST S.r.l. IRCCS
NCT number
NCT04300101

What you commit to

  • Study type: Observational
  • Planned participants: 300
  • From 14 May 2020 to the primary completion date, May 2026
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Patients included in clinical trials.

Who the study is looking for

  • New diagnosis of High grade Diffuse large B cell Lymphoma undergoing first line standard treatment;
  • Signed written informed consent;
  • Availability of FFPE sample.
  • Diagnosis of High grade Diffuse large B cell Lymphoma from 2011 to 2017;
  • Availability of FFPE sample and clinical data.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
L'Azienda Ospedaliero-Universitaria Di Bologna Policlinico S. Orsola-Malpighi
Coordinator of this site? Confirm its status
BolognaItalyRecruiting
Irst-Irccs
Coordinator of this site? Confirm its status
MeldolaItalyRecruiting
Ospedale S. Maria delle Croci RAVENNA
Coordinator of this site? Confirm its status
RavennaItalyRecruiting
Ospedale "Infermi"
Coordinator of this site? Confirm its status
RiminiItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.