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Current applications of multiparameter flow cytometry in plasma cell disorders

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F17%3A00068637" target="_blank" >RIV/65269705:_____/17:00068637 - isvavai.cz</a>

  • Alternative codes found

    RIV/61988987:17110/17:A1801RYG RIV/00843989:_____/17:E0106608

  • Result on the web

    <a href="http://www.nature.com/articles/bcj201790#change-history" target="_blank" >http://www.nature.com/articles/bcj201790#change-history</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1038/bcj.2017.90" target="_blank" >10.1038/bcj.2017.90</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Current applications of multiparameter flow cytometry in plasma cell disorders

  • Original language description

    Multiparameter flow cytometry (MFC) has become standard in the management of patients with plasma cell (PC) dyscrasias, and could be considered mandatory in specific areas of routine clinical practice. It plays a significant role during the differential diagnostic workup because of its fast and conclusive readout of PC clonality, and simultaneously provides prognostic information in most monoclonal gammopathies. Recent advances in the treatment and outcomes of multiple myeloma led to the implementation of new response criteria, including minimal residual disease (MRD) status as one of the most relevant clinical endpoints with the potential to act as surrogate for survival. Recent technical progress led to the development of next-generation flow (NGF) cytometry that represents a validated, highly sensitive, cost-effective and widely available technique for standardized MRD evaluation, which also could be used for the detection of circulating tumor cells. Here we review current applications of MFC and NGF in most PC disorders including the less frequent solitary plasmocytoma, light-chain amyloidosis or Waldenstrom macroglobulinemia.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30204 - Oncology

Result continuities

  • Project

    <a href="/en/project/NV17-30089A" target="_blank" >NV17-30089A: In-depth genomic analysis of residual clone in multiple myeloma: approach for individualized targeted therapy</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2017

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Blood cancer journal

  • ISSN

    2044-5385

  • e-ISSN

  • Volume of the periodical

    7

  • Issue of the periodical within the volume

    OCT 20

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    12

  • Pages from-to

    "e617"

  • UT code for WoS article

    000413469800001

  • EID of the result in the Scopus database

    2-s2.0-85047752896