Informace o publikaci

Necessity of flow cytometry assessment of circulating plasma cells and its connection with clinical characteristics of primary and secondary plasma cell leukaemia

Autoři	BEZDĚKOVÁ Renata JELINEK Tomas KRÁLOVÁ Romana ŠTORK Martin POLACKOVA Petra VŠIANSKÁ Pavla KUBÍNOVÁ Lucie JARKOVSKÝ Jiří ALMÁŠI Martina BOICHUK Ivanna KNECHTOVA Zdenka PENKA Miroslav POUR Luděk ŠEVČÍKOVÁ Sabina HAJEK Roman ŘÍHOVÁ Lucie
Rok publikování	2021
Druh	Článek v odborném periodiku
Časopis / Zdroj	British journal of haematology
Fakulta / Pracoviště MU	Lékařská fakulta
Citace
www	https://onlinelibrary.wiley.com/doi/10.1111/bjh.17713
Doi	http://dx.doi.org/10.1111/bjh.17713
Klíčová slova	plasma cell leukaemia; multiple myeloma; plasma cell; flow cytometry; prognosis; phenotype
Popis	Plasma cell leukaemia (PCL) is a rare and very aggressive plasma cell disorder. Preventing a dismal outcome of PCL requires early diagnosis with appropriate analytical tools. Therefore, the investigation of 33 patients with primary and secondary PCL was done when the quantity of circulating plasma cells (PCs) using flow cytometry (FC) and morphology assessment was evaluated. The phenotypic profile of the PCs was also analysed to determine if there is an association with clinical outcomes and to evaluate the prognostic value of analysed markers. Our results revealed that FC is an excellent method for identifying circulating PCs as a significantly higher number was identified by FC than by morphology (26 center dot 7% vs. 13 center dot 5%, P = 0 center dot 02). None of secondary PCL cases expressed CD19 or CD20. A low level of expression with similar positivity of CD27, CD28, CD81 and CD117 was found in both PCL groups. A decrease of CD44 expression was detected only in secondary PCL. Expression of CD56 was present in more than half of PCL cases as well as cytoplasmic nestin. A decreased level of platelets, Eastern Cooperative Oncology Group score of 2-3 and lack of CD20(+) PC were associated with a higher risk of death. FC could be incorporated in PCL diagnostics not only to determine the number of circulating PCs, but also to assess their phenotype profile and this information should be useful in patients' diagnosis and possible prognosis.