Clinical and Biological Characteristics of Medullary and Extramedullary Plasma Cell Dyscrasias

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Clinical and Biological Characteristics of Medullary and Extramedullary Plasma Cell Dyscrasias. / Janjetovic, Snjezana; Lohneis, Philipp; Nogai, Axel; Balci, Derya; Rasche, Leo; Jähne, Doris; Bokemeyer, Carsten; Schilling, Georgia; Blau, Igor Wolfgang; Schmidt-Hieber, Martin.

In: BIOLOGY-BASEL, Vol. 10, No. 7, 629, 06.07.2021.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Janjetovic, S, Lohneis, P, Nogai, A, Balci, D, Rasche, L, Jähne, D, Bokemeyer, C, Schilling, G, Blau, IW & Schmidt-Hieber, M 2021, 'Clinical and Biological Characteristics of Medullary and Extramedullary Plasma Cell Dyscrasias', BIOLOGY-BASEL, vol. 10, no. 7, 629. https://doi.org/10.3390/biology10070629

APA

Janjetovic, S., Lohneis, P., Nogai, A., Balci, D., Rasche, L., Jähne, D., Bokemeyer, C., Schilling, G., Blau, I. W., & Schmidt-Hieber, M. (2021). Clinical and Biological Characteristics of Medullary and Extramedullary Plasma Cell Dyscrasias. BIOLOGY-BASEL, 10(7), [629]. https://doi.org/10.3390/biology10070629

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Bibtex

@article{dac7553159af48a3a45b90c8989705a5,
title = "Clinical and Biological Characteristics of Medullary and Extramedullary Plasma Cell Dyscrasias",
abstract = "Background: Extramedullary plasma cell (PC) disorders may occur as extramedullary disease in multiple myeloma (MM-EMD) or as primary extramedullary plasmocytoma (pEMP)/solitary osseous plasmocytoma (SOP). In this study, we aimed to obtain insights into the molecular mechanisms of extramedullary spread of clonal PC. Methods: Clinical and biological characteristics of 87 patients with MM-EMD (n = 49), pEMP/SOP (n = 20) and classical MM (n = 18) were analyzed by using immunohistochemistry (CXCR4, CD31, CD44 and CD81 staining) and cytoplasmic immunoglobulin staining combined with fluorescence in situ hybridization (cIg-FISH). Results: High expression of CD44, a cell-surface glycoprotein involved in cell-cell interactions, was significantly enriched in MM-EMD (90%) vs. pEMP/SOP (27%) or classical MM (33%) (p < 0.001). In addition, 1q21 amplification by clonal PC occurred at a similar frequency of MM-EMD (33%), pEMP/SOP (57%) and classical MM (44%). Conversely, del(17p13), t(4;14) and t(14;16) were completely absent in pEMP/SOP. Besides this, 1q21 amplification was identified in 64% of not paraskeletal samples from MM-EMD or pEMP compared to 9% of SOP or paraskeletal MM-EMD/pEMP and 44% of classical MM samples, respectively (p = 0.02). Conclusion: Expression of molecules involved in homing and cytogenetic aberrations differ between MM with or without EMD and pEMP/SOP.",
author = "Snjezana Janjetovic and Philipp Lohneis and Axel Nogai and Derya Balci and Leo Rasche and Doris J{\"a}hne and Carsten Bokemeyer and Georgia Schilling and Blau, {Igor Wolfgang} and Martin Schmidt-Hieber",
year = "2021",
month = jul,
day = "6",
doi = "10.3390/biology10070629",
language = "English",
volume = "10",
journal = "BIOLOGY-BASEL",
issn = "2079-7737",
publisher = "Multidisciplinary Digital Publishing Institute (MDPI)",
number = "7",

}

RIS

TY - JOUR

T1 - Clinical and Biological Characteristics of Medullary and Extramedullary Plasma Cell Dyscrasias

AU - Janjetovic, Snjezana

AU - Lohneis, Philipp

AU - Nogai, Axel

AU - Balci, Derya

AU - Rasche, Leo

AU - Jähne, Doris

AU - Bokemeyer, Carsten

AU - Schilling, Georgia

AU - Blau, Igor Wolfgang

AU - Schmidt-Hieber, Martin

PY - 2021/7/6

Y1 - 2021/7/6

N2 - Background: Extramedullary plasma cell (PC) disorders may occur as extramedullary disease in multiple myeloma (MM-EMD) or as primary extramedullary plasmocytoma (pEMP)/solitary osseous plasmocytoma (SOP). In this study, we aimed to obtain insights into the molecular mechanisms of extramedullary spread of clonal PC. Methods: Clinical and biological characteristics of 87 patients with MM-EMD (n = 49), pEMP/SOP (n = 20) and classical MM (n = 18) were analyzed by using immunohistochemistry (CXCR4, CD31, CD44 and CD81 staining) and cytoplasmic immunoglobulin staining combined with fluorescence in situ hybridization (cIg-FISH). Results: High expression of CD44, a cell-surface glycoprotein involved in cell-cell interactions, was significantly enriched in MM-EMD (90%) vs. pEMP/SOP (27%) or classical MM (33%) (p < 0.001). In addition, 1q21 amplification by clonal PC occurred at a similar frequency of MM-EMD (33%), pEMP/SOP (57%) and classical MM (44%). Conversely, del(17p13), t(4;14) and t(14;16) were completely absent in pEMP/SOP. Besides this, 1q21 amplification was identified in 64% of not paraskeletal samples from MM-EMD or pEMP compared to 9% of SOP or paraskeletal MM-EMD/pEMP and 44% of classical MM samples, respectively (p = 0.02). Conclusion: Expression of molecules involved in homing and cytogenetic aberrations differ between MM with or without EMD and pEMP/SOP.

AB - Background: Extramedullary plasma cell (PC) disorders may occur as extramedullary disease in multiple myeloma (MM-EMD) or as primary extramedullary plasmocytoma (pEMP)/solitary osseous plasmocytoma (SOP). In this study, we aimed to obtain insights into the molecular mechanisms of extramedullary spread of clonal PC. Methods: Clinical and biological characteristics of 87 patients with MM-EMD (n = 49), pEMP/SOP (n = 20) and classical MM (n = 18) were analyzed by using immunohistochemistry (CXCR4, CD31, CD44 and CD81 staining) and cytoplasmic immunoglobulin staining combined with fluorescence in situ hybridization (cIg-FISH). Results: High expression of CD44, a cell-surface glycoprotein involved in cell-cell interactions, was significantly enriched in MM-EMD (90%) vs. pEMP/SOP (27%) or classical MM (33%) (p < 0.001). In addition, 1q21 amplification by clonal PC occurred at a similar frequency of MM-EMD (33%), pEMP/SOP (57%) and classical MM (44%). Conversely, del(17p13), t(4;14) and t(14;16) were completely absent in pEMP/SOP. Besides this, 1q21 amplification was identified in 64% of not paraskeletal samples from MM-EMD or pEMP compared to 9% of SOP or paraskeletal MM-EMD/pEMP and 44% of classical MM samples, respectively (p = 0.02). Conclusion: Expression of molecules involved in homing and cytogenetic aberrations differ between MM with or without EMD and pEMP/SOP.

U2 - 10.3390/biology10070629

DO - 10.3390/biology10070629

M3 - SCORING: Journal article

C2 - 34356484

VL - 10

JO - BIOLOGY-BASEL

JF - BIOLOGY-BASEL

SN - 2079-7737

IS - 7

M1 - 629

ER -