Clinical Relevance of Multicolour Flow Cytometry in Plasma Cell Disorders

被引:7
作者
Chatterjee, Gaurav [1 ]
Gujral, Sumeet [1 ]
Subramanian, Papagudi G. [1 ]
Tembhare, Prashant R. [1 ]
机构
[1] Tata Mem Hosp, Hematopathol Lab, ACTREC, Room 17-18,CCE Bldg, Navi Mumbai 410210, Maharashtra, India
关键词
Flow cytometry; Plasma cell disorders; Multiple myeloma; MINIMAL RESIDUAL DISEASE; BONE-MARROW MICROENVIRONMENT; ACUTE LYMPHOBLASTIC-LEUKEMIA; SMOLDERING MULTIPLE-MYELOMA; LIGHT-CHAIN AMYLOIDOSIS; MONOCLONAL GAMMOPATHY; UNDETERMINED SIGNIFICANCE; WALDENSTROMS MACROGLOBULINEMIA; DIFFERENTIAL-DIAGNOSIS; PROLIFERATIVE ACTIVITY;
D O I
10.1007/s12288-017-0822-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Multicolor flow cytometric (MFC) immunophenotyping is one of the basic test that is needed in the evaluation of hematolymphoid malignancies. Previously, there has been some reluctance in the use of MFC in plasma cell disorders (PCD). It was mainly due tolack of standardization, inadequate experience and detection of the lower number of plasma cells by MFC as compared to morphology. However, MFC has gone through many technological advancements in the last few years and a wide variety of reagents are now commercially available which worldwide allowed the establishment of standardized sensitive MFC-based immunophenotypic assay for PCD. Various studies have proven that MFC has a high clinical relevance in the diagnosis and risk stratification of multiple myeloma, its precursor conditions and other PCDs. Moreover, recent studies have shown that MFC is a highly sensitive and reliable technique for the monitoring of clinical response in the era of novel therapies. In this review, we have discussed the various applications of MFC in the management of PCD and their clinical relevance.
引用
收藏
页码:303 / 315
页数:13
相关论文
共 93 条
  • [1] Monoclonal Gammopathy of Undetermined Significance and Smoldering Multiple Myeloma: A Review of the Current Understanding of Epidemiology, Biology, Risk Stratification, and Management of Myeloma Precursor Disease
    Agarwal, Amit
    Ghobrial, Irene M.
    [J]. CLINICAL CANCER RESEARCH, 2013, 19 (05) : 985 - 994
  • [2] Almeida J, 1999, PATHOL BIOL, V47, P119
  • [3] Bataille R, 2006, HAEMATOLOGICA, V91, P1234
  • [4] Braham Jmili N, 2009, Clin Lab Sci, V22, P208
  • [5] BONE-MARROW MICROENVIRONMENT AND THE PROGRESSION OF MULTIPLE-MYELOMA
    CALIGARISCAPPIO, F
    GREGORETTI, MG
    MERICO, F
    GOTTARDI, D
    GHIA, P
    PARVIS, G
    BERGUI, L
    [J]. LEUKEMIA & LYMPHOMA, 1992, 8 (1-2) : 15 - 22
  • [6] Minimal residual disease monitoring in multiple myeloma
    Davies, FE
    Rawstron, RC
    Owen, RG
    Morgan, GJ
    [J]. BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY, 2002, 15 (01) : 197 - 222
  • [7] Immunophenotype of neoplastic plasma cells in AL amyloidosis
    Deshmukh, M.
    Elderfield, K.
    Rahemtulla, A.
    Naresh, K. N.
    [J]. JOURNAL OF CLINICAL PATHOLOGY, 2009, 62 (08) : 724 - 730
  • [8] The cellular immune system in myelomagenesis: NK cells and T cells in the development of MM and their uses in immunotherapies
    Dosani, T.
    Carlsten, M.
    Maric, I.
    Landgren, O.
    [J]. BLOOD CANCER JOURNAL, 2015, 5 : e306 - e306
  • [9] Treatment of multiple myeloma with the immunostimulatory SLAMF7 antibody elotuzumab
    Einsele, Hermann
    Schreder, Martin
    [J]. THERAPEUTIC ADVANCES IN HEMATOLOGY, 2016, 7 (05) : 288 - 301
  • [10] Flow cytometry in immunoglobulin light chain amyloidosis: Short review
    Filipova, Jana
    Rihova, Lucie
    Vsianska, Pavia
    Kufova, Zuzana
    Kryukova, Elena
    Kryukov, Fedor
    Hajek, Roman
    [J]. LEUKEMIA RESEARCH, 2015, 39 (11) : 1131 - 1136