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Spanish Registry of Patients With IgM Monoclonal Gammopathies

Spanish Registry of Patients With Diagnosis of IgM-MGUS, Asymptomatic & Symptomatic Waldenström Macroglobulinemia. Analysis of Clinical and Laboratory Features, Treatment and Outcomes.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05093153
Acronym
PRAME
Enrollment
1000
Registered
2021-10-26
Start date
2021-10-01
Completion date
2030-03-01
Last updated
2026-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Waldenstrom Macroglobulinemia

Brief summary

Waldenström's macroglobulinemia (WM) is a B-cell lymphoproliferative disorder which is defined by bone marrow infiltration by small lymphocytes, lymphoplasmacytoid and plasma cells together with the presence of a detectable monoclonal immunoglobulin M (IgM).The clinical presentation of WM is variable. Symptoms can be related to tumor infiltration, or they can be related to the monoclonal IgM component. The therapeutic options are heterogeneous and there are no well-established in both first line or relapse/refractory settings. In Spain, the incidence of MGUS-IgM and WM in the last decade is unknown. The aims of this retrospective, observational, multicentric study is: * To develop a national registry of patients diagnosed with Waldenström's Macroglobulinemia and Monoclonal Gammopathy of uncertain significance -IgM in Spain in the past 30years. * To evaluate the most relevant clinical characteristics, long-term safety and efficacy of different therapeutic schemes and long-term prognosis of patients with WM * To help in the design of future therapeutic strategies, risk prognostic factors and clinical trials in Spain. Methods: The investigators will collect data from the patient clinical files after prior Informed Consent providing from patients with diagnosis of MGUS-IgM and WM in the past 30 years in Spain, according to the WHO classification of lymphoid tumors (2008) revised in 2016. Data from patients not able to provide IC (i.e., already dead patients) will be included only after the permission of the ethics review board. The collected data will be included in a database of the Spanish Myeloma and Lymphoma Intergroup (SMALI) team created ad-hoc by the Spanish Society of Hematology and Hemotherapy (SEHH). Each principal investigator in each center will conduct their technical supervision. The evaluation of the treatment protocols will be done following the indications of the intergroup committee according to the guidelines of the International Waldenström's Macroglobulinemia Group.

Interventions

None listed

Sponsors

Fundación Española de Hematología y Hemoterapía
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥18 years * Patients having a confirmed diagnosis of either in the las 30 years: * Monoclonal Gammopathy of uncertain significance -IgM * Asymptomatic Waldenström's macroglobulinemia * Symptomatic Waldenström's macroglobulinemia

Exclusion criteria

* Other subtypes of Lymphoproliferative diseases.

Design outcomes

Primary

MeasureTime frameDescription
Overall survivalthrough study completion, an average of 4 yearsOverall survival evaluation from the date of diagnosis to the death of the patient due to any cause

Countries

Spain

Contacts

CONTACTRAMON GARCIA SANZ, MD
rgarcias@usal.es+34 915868000
CONTACTELHAM ASKARI ASKARI, MD
easkari@fdj.es+34 915504800

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026