TY - JOUR
T1 - International Myeloma Working Group risk stratification model for smoldering multiple myeloma (SMM)
AU - Mateos, María Victoria
AU - Kumar, Shaji
AU - Dimopoulos, Meletios A.
AU - González-Calle, Verónica
AU - Kastritis, Efstathios
AU - Hajek, Roman
AU - De Larrea, Carlos Fernández
AU - Morgan, Gareth J.
AU - Merlini, Giampaolo
AU - Goldschmidt, Hartmut
AU - Geraldes, Catarina
AU - Gozzetti, Alessandro
AU - Kyriakou, Charalampia
AU - Garderet, Laurent
AU - Hansson, Markus
AU - Zamagni, Elena
AU - Fantl, Dorotea
AU - Leleu, Xavier
AU - Kim, Byung Su
AU - Esteves, Graça
AU - Ludwig, Heinz
AU - Usmani, Saad
AU - Min, Chang Ki
AU - Qi, Ming
AU - Ukropec, Jon
AU - Weiss, Brendan M.
AU - Rajkumar, S. Vincent
AU - Durie, Brian G.M.
AU - San-Miguel, Jesús
N1 - Funding Information:
We would like to acknowledge Amirah Limayo and Lisa Paik at the International Myeloma Foundation for their contribution and Anja Haltner, Steven Doucette, and Chris at the Cornerstone group for their role in the statistical analysis. The data collection study was conducted by the International Myeloma Foundation as an International Myeloma Working Group project supported in part by a grant funded by Janssen.
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/10/1
Y1 - 2020/10/1
N2 - 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.
AB - 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.
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U2 - 10.1038/s41408-020-00366-3
DO - 10.1038/s41408-020-00366-3
M3 - Article
C2 - 33067414
AN - SCOPUS:85092644198
SN - 2044-5385
VL - 10
JO - Blood cancer journal
JF - Blood cancer journal
IS - 10
M1 - 102
ER -