Blood cancer journal · 2018
Risk stratification of smoldering multiple myeloma incorporating revised IMWG diagnostic criteria.
СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод пока не подготовлен
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Lakshman Arjun, Rajkumar S Vincent, Buadi Francis K, Binder Moritz, Gertz Morie A, Lacy Martha Q, Dispenzieri Angela, Dingli David, Fonder Amie L, Hayman Suzanne R, Hobbs Miriam A, Gonsalves Wilson I, Hwa Yi Lisa, Kapoor Prashant, Leung Nelson, Go Ronald S, Lin Yi, Kourelis Taxiarchis V, Warsame Rahma, Lust John A, Russell Stephen J, Zeldenrust Steven R, Kyle Robert A, Kumar Shaji K
Аннотация
In 2014, the International Myeloma Working Group reclassified patients with smoldering multiple myeloma (SMM) and bone marrow-plasma cell percentage (BMPC%) ≥ 60%, or serum free light chain ratio (FLCr) ≥ 100 or >1 focal lesion on magnetic resonance imaging as multiple myeloma (MM). Predictors of progression in patients currently classified as SMM are not known. We identified 421 patients with SMM, diagnosed between 2003 and 2015. The median time to progression (TTP) was 57 months (CI, 45-72). BMPC% > 20% [hazard ratio (HR): 2.28 (CI, 1.63-3.20); p < 0.0001]; M-protein > 2g/dL [HR: 1.56 (CI, 1.11-2.20); p = 0.01], and FLCr > 20 [HR: 2.13 (CI, 1.55-2.93); p < 0.0001] independently predicted shorter TTP in multivariate analysis. Age and immunoparesis were not significant. We stratified patients into three groups: low risk (none of the three risk factors; n = 143); intermediate risk (one of the three risk factors; n = 121); and high risk (≥2 of the three risk factors; n = 153). The median TTP for low-, intermediate-, and high-risk groups were 110, 68, and 29 months, respectively (p < 0.0001). BMPC% > 20%, M-protein > 2 g/dL, and FLCr > 20 at diagnosis can be used to risk stratify patients with SMM. Patients with high-risk SMM need close follow-up and are candidates for clinical trials aiming to prevent progression.