Immunoglobulin M Monoclonal Gammopathies of Undetermined Significance and Indolent Waldenström's Macroglobulinemia Recognize the Same Determinants of Evolution Into Symptomatic Lymphoid Disorders: Proposal for a Common Prognostic Scoring System

Author:

Baldini Luca1,Goldaniga Maria1,Guffanti Andrea1,Broglia Chiara1,Cortelazzo Sergio1,Rossi Andrea1,Morra Enrica1,Colombi Mariangela1,Callea Vincenzo1,Pogliani Enrico1,Ilariucci Fiorella1,Luminari Stefano1,Morel Pierre1,Merlini Giampaolo1,Gobbi Paolo1

Affiliation:

1. From the Unità Operativa Ematologia 1, Dipartimento di Ematologia e Oncologia, Ospedale Maggiore, I.R.C.C.S; Divisione di Medicina I, Ospedale “Fatebenefratelli e Oftalmico”; Divisione di Ematologia, Ospedale Niguarda, Cà Granda, Milan; Dipartimento di Medicina Interna e Oncologia Medica, Università degli Studi, Policlinico S. Matteo, I.R.C.C.S., Pavia; Divisione di Ematologia, Ospedali Riuniti, Bergamo; Dipartimento di Ematologia, Azienda Ospedaliera Bianchi-Melacrino-Morelli, Reggio Calabria;...

Abstract

Purpose To evaluate the clinicohematologic variables at diagnosis that are prognostically related to neoplastic progression in patients with immunoglobulin M (IgM) monoclonal gammopathies of undetermined significance (MGUS), and indolent Waldenström's macroglobulinemia (IWM), and propose a scoring system to identify subsets of patients at different risk. Patients and Methods We evaluated 217 patients with IgM MGUS and 201 with IWM (male-female ratio, 131:86 and 117:84; mean age, 63.7 and 63.6 years, respectively) diagnosed on the basis of serum monoclonal component (MC) levels and bone marrow lymphoplasmacytic infiltration degree. The variables selected by univariate analyses were multivariately investigated; on the basis of their individual relative hazards, a scoring system was devised to identify subsets of patients at different risk of evolution. Results After a median follow-up of 56.1 and 60.2 months, 15 of 217 MGUS and 45 of 201 IWM patients, respectively, required chemotherapy for symptomatic WM (13 and 36), non-Hodgkin's lymphoma (2 and 6) and amyloidosis (0 and 3). The median time to evolution (TTE) was not reached for MGUS and was 141.5 months for IWM. The variables adversely related to evolution were qualitatively the same in both groups: MC levels, Hb concentrations and sex. A scoring system based on these parameters identified three risk groups with highly significant differences in TTE in both groups (P < .0001). Conclusion MGUS and IWM identify disease entities with different propensities for symptomatic neoplastic evolution. As both have the same prognostic determinants of progression, we propose a practical scoring system that, identifying different risks of malignant evolution, may allow an individualized clinical approach.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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