MGRS: Clinical-histological Features of a Multicenter Case Series

Sponsor
University of Milano Bicocca (Other)
Overall Status
Recruiting
CT.gov ID
NCT05119309
Collaborator
(none)
180
8
13.6
22.5
1.7

Study Details

Study Description

Brief Summary

The term "Monoclonal Gammopathies of Renal Significance" (MGRS) describes a group of diseases characterized by the presence of an immunoglobulin or monoclonal immunoglobulin fraction that has the ability to cause renal damage.

It is important to diagnose MGRS correctly and early as renal survival depends on the renal function present at the time of diagnosis and it is necessary to establish a specific treatment that aims to stop the progression of the damage. organ and restoration of renal function.

To date, there are no targeted therapeutic strategies that can prevent the formation of deposits or that can eliminate the deposits already present in the kidney, which constitute the etiopathogenetic factor of these pathologies. Therefore, the only valid therapeutic option is to act against the clone of B lymphocytes underlying the nephrological pathology, although it is not a clone with such requirements to be able to define it as a tumor.

Therefore, given the absence of a well-defined policy in the therapy of MGRS and the doubts present on the validity of a therapeutic approach aimed at the suppression of a plasma cell clone, the investigators decided to carry out an observational retrospective study with the aim of describing, in a large series of MGRS treated with oncohematological therapy, the renal and overall outcome of patients and identify any presenting prognostic characteristics that can help improve the diagnosis of these disorders and the long-term survival of patients.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The group will be compared with patients suffering from renal disease associated with oncohematological diseases with full clinical expression (multiple myeloma and B cell lymphomas) which produce monoclonal component and who have been treated according to the established specific schemes of each disease.

    The study will have a total duration of 12 months. It will analyze the data of the patients included in the clinical charts from 01/01/2010 to 31/12/2020. A total of 120 patients and 60 pathological controls will be enrolled (2:1 ratio), expected total number of patients from the centers participating in the study enrolled through the outpatient clinics of the Departments of the study.

    The variables considered in the study are routine laboratory data (renal function, electrophoresis of serum and urinary proteins with immunofission, serum free light chains and their ratio, proteinuria 24 h serum albumin), clinical and anamnestic data, data on current drug therapy and description of renal biopsy characteristics using a predefined database with statistical analysis of data.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    180 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Monoclonal Gammopathies of Renal Significance: Clinical-histological Features of a Multicenter Case Series (MGRS Project)
    Actual Study Start Date :
    Jul 15, 2021
    Anticipated Primary Completion Date :
    Sep 1, 2022
    Anticipated Study Completion Date :
    Sep 1, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    patient group

    Renal biopsy diagnosis of MGRS or disease linked to multiple myeloma and B cell lymphoma

    control patient group

    Renal biopsy diagnosis of nephropathy linked to onco-haematological pathology with full clinical expression (Multiple Myeloma, B-cell Lymphoma)

    Outcome Measures

    Primary Outcome Measures

    1. Assessment of pictures of biochemical presentation [through study completion, an average of 1 year]

      Multicenter retrospective evaluation of biochemical presentation pictures of patients with MGRS and clinically expressed haematological diseases, with renal involvement

    Secondary Outcome Measures

    1. Evaluation of the renal status of study patients using physiological parameters (use of the eGFR in ml / min / 1.73 m2 calculated with CKD-EPI) [through study completion, an average of 1 year]

      Renal and global health outcomes of patients with MGRS, comparison with patients with haematological diseases

    2. Evaluation of the global health of study patients using physiological parameters (use of the eGFR in ml / min / 1.73 m2 calculated with CKD-EPI) [through study completion, an average of 1 year]

      Renal and global health outcomes of patients with MGRS, comparison with patients with haematological diseases

    3. Prognostic characteristics [through study completion, an average of 1 year]

      Identification of any prognostic characteristics of presentation

    4. Biochemical indicators of response to treatment [through study completion, an average of 1 year]

      Identification of any biochemical indicators of response to treatment (serum and urinary protein electrophoresis and 24 h proteinuria to evaluate renal function)

    5. Clinical indicators of response to treatment [through study completion, an average of 1 year]

      Identification of any biochemical and clinical indicators of response to treatment (serum and urinary protein electrophoresis and 24 h proteinuria to evaluate renal function)

    6. Therapies [through study completion, an average of 1 year]

      Description of the therapies applied in the treatment of pathologies, report of side effects

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 100 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Renal biopsy diagnosis of MGRS or disease linked to multiple myeloma and B cell lymphoma between 01/01/2010 and 31/12/2020 (for patient group)

    • Renal biopsy diagnosis of nephropathy linked to onco-haematological pathology with full clinical expression (eg Multiple Myeloma, B-cell Lymphoma) between 01/01/2010 and 31/12/2021 (for control group);

    • Age greater than or equal to 18 years;

    • Informed consent freely granted and acquired before the start of the study.

    Exclusion Criteria:
    • Patients who do not meet the relevant inclusion criteria and who do not have an established diagnosis of MGRS or disease related to multiple myeloma and B-cell lymphoma will be excluded from the study.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 ASST Lariana, Ospedale Sant' Anna San Fermo Della Battaglia Como Italy 22020
    2 ASST Nord Milano, Presidio Ospedaliero Bassini Cinisello Balsamo Milano Italy 20092
    3 IRCCS Istituto Clinico Humanitas Rozzano Milano Italy 20089
    4 ASST Monza, Ospedale di Desio Desio Monza E Brianza Italy 20832
    5 ASST Lecco, Presidio Ospedaliero Alessandro Manzoni Lecco Italy 23900
    6 Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milano Italy 20122
    7 ASST Monza Monza Italy 20900
    8 ASST Sette Laghi, Ospedale di Circolo e Fondazione Macchi Varese Italy 21100

    Sponsors and Collaborators

    • University of Milano Bicocca

    Investigators

    • Principal Investigator: Renato A Sinico, MD, Università degli Studi di Milano Bicocca

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Milano Bicocca
    ClinicalTrials.gov Identifier:
    NCT05119309
    Other Study ID Numbers:
    • MGRS
    First Posted:
    Nov 15, 2021
    Last Update Posted:
    Jul 21, 2022
    Last Verified:
    Jul 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by University of Milano Bicocca
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 21, 2022