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The Current State of Knowledge About Evolution of Multiple Myeloma to Plasma Cell Leukemia
Artur Jurczyszyn1, Magdalena Olszewska-Szopa2, David H Vesole3
1Hematology Department, Jagiellonian University Medical College, Cracow, Poland.
Abstract:
Plasma cell leukemia is a rare form of multiple myeloma (MM). In contrast to de novo primary plasma cell leukemia (pPCL), which is very uncommon presentation of MM, there is increasing frequency of transformation to secondary plasma cell leukemia (sPCL) with increasing survival of patients (MM). The molecular basis of sPCL remains poorly understood sPCL is particularly aggressive and is associated with an extremely poor prognosis, constituting a major unmet medical need. High-quality data in sPCL regarding presentation, treatment and outcomes is limited. Herein we review the current state of knowledge on sPCL diagnostics, molecular biology, clinical characteristics, prognosis and reported treatment outcomes and the emergence of the new therapeutic strategies.
Insights
Secondary plasma cell leukemia (sPCL) is an aggressive multiple myeloma (MM) complication. Understanding sPCL
Area of Science:
- Hematology
- Oncology
- Molecular Biology
Background:
- Multiple myeloma (MM) survival is increasing, leading to more secondary plasma cell leukemia (sPCL) cases.
- Primary plasma cell leukemia (pPCL) is a rare MM presentation.
- Secondary plasma cell leukemia (sPCL) is a transformation from MM.
Observation:
- Secondary plasma cell leukemia (sPCL) is aggressive with a poor prognosis.
- Data on sPCL presentation, treatment, and outcomes is limited.
- The molecular basis of sPCL is poorly understood.
Findings:
- This review synthesizes current knowledge on sPCL.
- It covers diagnostics, molecular biology, clinical characteristics, and prognosis.
- Emerging therapeutic strategies for sPCL are discussed.
Implications:
- Addressing the unmet medical need in sPCL is crucial.
- Improved understanding can guide treatment strategies.
- Further research into sPCL molecular biology is warranted.
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