Cytokine profile in multiple myeloma

•Cytokines play a crucial role in the growth, survival and dissemination of malignant plasma cells in myeloma.•IL-6 is a key cytokine.•Increased cytokine levels are seen at relapse compared to levels at diagnosis.•Treatment modulates abnormal cytokine functions.•Cytokine levels may predict survival...

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Veröffentlicht in:Cytokine (Philadelphia, Pa.) Pa.), 2020-12, Vol.136, p.155271-155271, Article 155271
Hauptverfasser: Jasrotia, Shivali, Gupta, Ritu, Sharma, Atul, Halder, Ashutosh, Kumar, Lalit
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Sprache:eng
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Zusammenfassung:•Cytokines play a crucial role in the growth, survival and dissemination of malignant plasma cells in myeloma.•IL-6 is a key cytokine.•Increased cytokine levels are seen at relapse compared to levels at diagnosis.•Treatment modulates abnormal cytokine functions.•Cytokine levels may predict survival in myeloma. Cytokines play a crucial role in the growth, survival and dissemination of malignant plasma cells in patients of multiple myeloma (MM). We estimated concentrations of five key cytokines: Vascular Endothelial Growth Factor (VEGF), Interleukin-6 (IL-6), Tumor Necrosis Factor- alpha (TNF- α), B-cell activating factor (BAFF), and Receptor Activator of Nuclear Factor-κB ligand (RANKL) in newly diagnosed and relapsed/refractory MM (RRMM). The study groups include 68 newly diagnosed and 21 relapsed/refractory (RR) MM patients. 32 out of 68 newly diagnosed MM patients were evaluated for serum cytokine concentrations after their treatment. For survival analysis, the various parameters were studied in relation to both progression free survival (PFS) and overall survival (OS). The median serum levels of VEGF, IL-6, BAFF and RANKL were higher in RRMM compared with newly diagnosed patients. However, the difference was significant for BAFF levels (p = 0.04). The median serum levels of VEGF, IL-6, TNF-α, BAFF and RANKL were significantly higher in newly diagnosed and RRMM patients, compared to controls. We also observed lower plasma levels of VEGF (p=
ISSN:1043-4666
1096-0023
DOI:10.1016/j.cyto.2020.155271