TY - JOUR
T1 - Smoldering multiple myeloma
T2 - Present position and potential promises
AU - Tageja, Nishant
AU - Manasanch, Elisabet E.
AU - Korde, Neha
AU - Kwok, Mary
AU - Mailankody, Sham
AU - Bhutani, Manisha
AU - Roschewski, Mark
AU - Landgren, Ola
PY - 2014/1
Y1 - 2014/1
N2 - Since smoldering multiple myeloma (SMM) was first described over three decades ago based on a case series of six patients, its definition and our understanding of the entity have evolved considerably. The risk of progression to symptomatic myeloma (MM) varies greatly among individuals diagnosed with myeloma precursor disease. Epidemiologic, molecular, flow cytometric and radiological techniques have demonstrated that this transformation to MM from precursor states is not sudden but rather a continuous overlapping series of events with evidence of end-organ damage that could manifest in the earliest stages of disease. Contemporary antimyeloma therapies can yield rapid, deep, and durable responses with manageable toxicities, and molecular-cell-based measures are now available to rule out minimal residual disease. With this information, clinical studies with correlative measures can now be developed to test the fundamental hypothesis that intervention in early myeloma may provide a measurable clinical benefit to patients by either delaying progression or eradicating plasma cell clones.
AB - Since smoldering multiple myeloma (SMM) was first described over three decades ago based on a case series of six patients, its definition and our understanding of the entity have evolved considerably. The risk of progression to symptomatic myeloma (MM) varies greatly among individuals diagnosed with myeloma precursor disease. Epidemiologic, molecular, flow cytometric and radiological techniques have demonstrated that this transformation to MM from precursor states is not sudden but rather a continuous overlapping series of events with evidence of end-organ damage that could manifest in the earliest stages of disease. Contemporary antimyeloma therapies can yield rapid, deep, and durable responses with manageable toxicities, and molecular-cell-based measures are now available to rule out minimal residual disease. With this information, clinical studies with correlative measures can now be developed to test the fundamental hypothesis that intervention in early myeloma may provide a measurable clinical benefit to patients by either delaying progression or eradicating plasma cell clones.
KW - Carfilzomib
KW - Flow cytometry
KW - Lenalidomide
KW - Multiple myeloma
KW - Plasma cell dyscrasia
KW - Smoldering myeloma
UR - http://www.scopus.com/inward/record.url?scp=84890145812&partnerID=8YFLogxK
U2 - 10.1111/ejh.12205
DO - 10.1111/ejh.12205
M3 - Review article
C2 - 24112232
AN - SCOPUS:84890145812
SN - 0902-4441
VL - 92
SP - 1
EP - 12
JO - European Journal of Haematology
JF - European Journal of Haematology
IS - 1
ER -