Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT07214324

Integrative Multi-omics Analysis to Predict Monoclonal Gammopathies Clinical Evolution

Led by Azienda USL Reggio Emilia - IRCCS · Updated on 2026-04-23

60

Participants Needed

4

Research Sites

93 weeks

Total Duration

On this page

Sponsors

A

Azienda USL Reggio Emilia - IRCCS

Lead Sponsor

E

European Union

Collaborating Sponsor

AI-Summary

What this Trial Is About

This prospective, multicenter, observational study aims to identify molecular and immunological markers associated with disease progression in patients with monoclonal gammopathy of undetermined significance (MGUS) and smoldering multiple myeloma (SMM). By integrating genomic, transcriptomic, immunophenotypic, and oral microbiome analyses, the study seeks to characterize the biological mechanisms underlying the transition to symptomatic multiple myeloma (MM). The study also includes in vitro modeling to investigate bone damage and immune dysfunction. Healthy volunteers (HV) undergoing joint replacement surgery for osteoarthritis will serve as controls. The ultimate goal is to improve early risk stratification and support future preventive strategies through a multi-omics approach. There is a pressing need for new strategies to identify high-risk individuals based on biological rather than purely clinical parameters. This study proposes an integrative, multi-omics approach to investigate the transition from MGUS/SMM to MM. By analyzing the immunome and oral microbiome alongside molecular profiling, the goal is to identify reliable biomarkers of progression. The resulting insights could be enable more accurate risk stratification and guide the design of future preventive clinical trials aimed at delaying or halting disease evolution.

CONDITIONS

Official Title

Integrative Multi-omics Analysis to Predict Monoclonal Gammopathies Clinical Evolution

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age over 18 years
  • Male or female patients
  • Histologically confirmed diagnosis of MGUS, SMM, or MM according to ESMO 2021 guidelines
  • Willing and able to provide written informed consent
  • Healthy volunteers over 60 years
  • Diagnosis of osteoarthritis
  • Scheduled for hospitalization for surgical treatment of osteoarthritis (endoprosthesis or arthroplasty)
  • Willing and able to provide written informed consent
Not Eligible

You will not qualify if you...

  • Active current infection
  • Autoimmune disease
  • Women of childbearing potential unable to exclude pregnancy
  • Use of high-dose corticosteroids within the past 7 days
  • Prior joint surgery or severe joint deformity (healthy volunteers)
  • Recent trauma, osteonecrosis, or osteoarthritis caused by prior or current joint infection (healthy volunteers)
  • Metabolic disorders (healthy volunteers)
  • Previous or current cancer diagnosis (healthy volunteers)
  • Autoimmune diseases such as rheumatoid arthritis (healthy volunteers)

AI-Screening

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Trial Site Locations

Total: 4 locations

1

Istituto Ortopedico Rizzoli IRCCS

Bologna, Italy

Active, Not Recruiting

2

UO Ematologia Azienda Ospedaliero-Universitaria "Policlinico Rodolico San Marco"

Catania, Italy

Active, Not Recruiting

3

UOC di Ematologia, Dipartimento di Oncologia, AOU Policlinico "Paolo Giaccone"

Palermo, Italy

Active, Not Recruiting

4

S.C Ematologia - Azienda USL IRCCS di Reggio Emilia

Reggio Emilia, Italy

Actively Recruiting

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Research Team

N

Noemi Puccio

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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