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International Myeloma Working Group risk stratification model for smoldering multiple myeloma (SMM)

Authors :
International Myeloma Foundation
Janssen Research and Development
Mateos, Maria Victoria
Kumar, Sumit
Dimopoulos, Meletios A.
González-Calle, Verónica
Kastritis, Efstathios
Hajek, Roman
Fernández de Larrea, Carlos
Morgan, Gareth J.
Merlini, Giampolo
Goldschmidt, Hartmut
Geraldes, Catarina
Gozzetti, Alessandro
Kyriakou, Charalampia
Garderet, Laurent
Hansson, Markus
Zamagni, Elena
Fantl, Dorotea
Leleu, Xavier
Kim, Byung-Su
Esteves, Graça
Ludwig, Heinz
Usmani, Saad Z.
Min, Chang-Ki
Qi, Ming
Ukropec, Jon
Weiss, Brendan M.
Rajkumar, S. Vincent
Durie, B.
San-Miguel, Jesús
International Myeloma Foundation
Janssen Research and Development
Mateos, Maria Victoria
Kumar, Sumit
Dimopoulos, Meletios A.
González-Calle, Verónica
Kastritis, Efstathios
Hajek, Roman
Fernández de Larrea, Carlos
Morgan, Gareth J.
Merlini, Giampolo
Goldschmidt, Hartmut
Geraldes, Catarina
Gozzetti, Alessandro
Kyriakou, Charalampia
Garderet, Laurent
Hansson, Markus
Zamagni, Elena
Fantl, Dorotea
Leleu, Xavier
Kim, Byung-Su
Esteves, Graça
Ludwig, Heinz
Usmani, Saad Z.
Min, Chang-Ki
Qi, Ming
Ukropec, Jon
Weiss, Brendan M.
Rajkumar, S. Vincent
Durie, B.
San-Miguel, Jesús
Publication Year :
2020

Abstract

Smoldering multiple myeloma (SMM) is an asymptomatic precursor state of multiple myeloma (MM). Recently, MM was redefined to include biomarkers predicting a high risk of progression from SMM, thus necessitating a redefinition of SMM and its risk stratification. We assembled a large cohort of SMM patients meeting the revised IMWG criteria to develop a new risk stratification system. We included 1996 patients, and using stepwise selection and multivariable analysis, we identified three independent factors predicting progression risk at 2 years: serum M-protein >2 g/dL (HR: 2.1), involved to uninvolved free light-chain ratio >20 (HR: 2.7), and marrow plasma cell infiltration >20% (HR: 2.4). This translates into 3 categories with increasing 2-year progression risk: 6% for low risk (38%; no risk factors, HR: 1); 18% for intermediate risk (33%; 1 factor; HR: 3.0), and 44% for high risk (29%; 2–3 factors). Addition of cytogenetic abnormalities (t(4;14), t(14;16), +1q, and/or del13q) allowed separation into 4 groups (low risk with 0, low intermediate risk with 1, intermediate risk with 2, and high risk with ≥3 risk factors) with 6, 23, 46, and 63% risk of progression in 2 years, respectively. The 2/20/20 risk stratification model can be easily implemented to identify high-risk SMM for clinical research and routine practice and will be widely applicable.

Details

Database :
OAIster
Publication Type :
Electronic Resource
Accession number :
edsoai.on1286560475
Document Type :
Electronic Resource