RecruitingNCT07214324

Integrative Multi-omics Analysis to Predict Monoclonal Gammopathies Clinical Evolution


Sponsor

Azienda USL Reggio Emilia - IRCCS

Enrollment

60 participants

Start Date

Mar 17, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Collection of biological material for people with monoclonal gammopathy of undetermined significance (mgus), multiple myeloma (mm), and other related conditions. The study is currently recruiting participants at 4 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERCollection of biological material

For MGUS, SMM and MM patients, biological material (bone marrow aspirate, bone marrow biopsy, peripheral blood) consists exclusively of left-over samples obtained during routine diagnostic procedures and clinical practice management of their disease. For healthy volunteers, biological material includes waste bone tissue obtained during orthopedic surgery (endo- or arthro-prosthesis) and peripheral blood collected for research purposes. Both cohort of patient will be asked to donate gingival crevicular fluid (GCF) (this is a non-invasive procedure with no associated risks).


Locations(4)

Istituto Ortopedico Rizzoli IRCCS

Bologna, Italy

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

Catania, Italy

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

Palermo, Italy

S.C Ematologia - Azienda USL IRCCS di Reggio Emilia

Reggio Emilia, Italy

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NCT07214324


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