Correlation of assessment of plasma cells by flow cytometry and detection of cytogenomic abnormalities by fluorescence in situ hybridization in plasma cell neoplasms

被引:1
|
作者
Lu, G. [1 ]
Zhang, X. X. [2 ]
You, M. J.
Chen, W. [3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Hematopathol, Unit 350, Houston, TX 77030 USA
[2] USLabs LabCorp, Brentwood, TN USA
[3] USLabs LabCorp, Irvine, CA USA
关键词
Plasma cell count; flow cytometry; fluorescence in situ hybridization; plasma cell neoplasm; MULTIPLE-MYELOMA; PROGNOSTIC-FACTOR; LEUKEMIA;
D O I
10.1111/j.1751-553X.2011.01323.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Increased monoclonal plasma cell count (PCC) in bone marrow (BM) is an indicator of a plasma cell neoplasm (PCN). Assessing PCC in BM by morphologic evaluation (ME) and flow cytometry (FC) is important in diagnosing PCN. Also important is fluorescence in situ hybridization (FISH) to detect cytogenomic abnormalities (CAs) in PCN. Owing to FC's short turnaround time, FC-assessed PCC is often used as empirical reference for further FISH study. However, correlation of FC-assessed PCs with FISH-detected CAs has not been well studied. The purpose of this study was to validate this correlation on BM aspirates from patients with PCN. Methods: We reviewed 224 cases of newly diagnosed PCN identified from our Lab-database. Both FC and FISH had been performed on BM aspirates from these cases, of which 178 had been assessed by ME. The original findings from the 224 cases were also reviewed. Results: Using a cut-off of 3% PCs assessed by FC as an indicator for further FISH analysis, 20 (17%) FISH-detectable PCN cases were missed; 30% of the missed cases carried high-risk CAs and/or were highly progressive PCN. Conclusion: In PCN cases, an FC-assessed 3% PCC in BM aspirates should not be used as a cut-off for further FISH testing.
引用
收藏
页码:545 / 550
页数:6
相关论文
共 50 条
  • [1] Plasma Cell Enrichment Enhances Detection of High-Risk Cytogenomic Abnormalities by Fluorescence In Situ Hybridization and Improves Risk Stratification of Patients With Plasma Cell Neoplasms
    Lu, Gary
    Muddasani, Ramya
    Orlowski, Robert Z.
    Abruzzo, Lynne V.
    Qazilbash, Muzaffar H.
    You, M. James
    Wang, Yaping
    Zhao, Ming
    Chen, Su
    Glitza, Isabella Claudia
    Medeiros, L. Jeffrey
    ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE, 2013, 137 (05) : 625 - 631
  • [2] Utility of Flow Cytometry and Fluorescence In Situ Hybridization in Follow-up Monitoring of Plasma Cell Myeloma
    Chopra, Saurav
    Dunham, Timothy
    Syrbu, Sergei, I
    Karandikar, Nitin J.
    Darbro, Benjamin W.
    Holman, Carol J.
    AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2021, 156 (02) : 198 - 204
  • [3] Interphase Fluorescence In Situ Hybridization on Selected Plasma Cells is Superior in the Detection of Cytogenetic Aberrations in Plasma Cell Dyscrasia
    Put, Natalie
    Lemmens, Heidi
    Wlodarska, Iwona
    Konings, Peter
    Moreau, Yves
    Hagemeijer, Anne
    Vandenberghe, Peter
    Michaux, Lucienne
    GENES CHROMOSOMES & CANCER, 2010, 49 (11) : 991 - 997
  • [4] Implementation of cytogenomic microarray with plasma cell enrichment enables better abnormality detection and risk stratification in patients with plasma cell neoplasia than conventional cytogenetics and fluorescence in situ hybridization
    Chen, Chuanfei
    Lim, Alvin Soon Tiong
    Lau, Lai Ching
    Lim, Tse Hui
    Heng, Evelyn Yee Hsieh
    Tien, Sim Leng
    CANCER GENETICS, 2021, 252 : 25 - 36
  • [5] Rapid detection and identification of pathogens in blood cultures by fluorescence in situ hybridization and flow cytometry
    Kempf, VAJ
    Mändle, T
    Schumacher, U
    Schäfer, A
    Autenrieth, IB
    INTERNATIONAL JOURNAL OF MEDICAL MICROBIOLOGY, 2005, 295 (01) : 47 - 55
  • [6] Flow cytometry and fluorescence in situ hybridization to detect residual neuroblastoma cells in bone marrow
    Okcu, MF
    Wang, RY
    Bueso-Ramos, C
    Schober, W
    Weidner, D
    Andrassy, R
    Blakely, M
    Russell, H
    Ozkan, A
    Kuttesch, J
    Andreeff, M
    Chan, KW
    Ater, J
    PEDIATRIC BLOOD & CANCER, 2005, 45 (06) : 787 - 795
  • [7] Necessity of flow cytometry assessment of circulating plasma cells and its connection with clinical characteristics of primary and secondary plasma cell leukaemia
    Bezdekova, Renata
    Jelinek, Tomas
    Kralova, Romana
    Stork, Martin
    Polackova, Petra
    Vsianska, Pavla
    Brozova, Lucie
    Jarkovsky, Jiri
    Almasi, Martina
    Boichuk, Ivanna
    Knechtova, Zdenka
    Penka, Miroslav
    Pour, Ludek
    Sevcikova, Sabina
    Hajek, Roman
    Rihova, Lucie
    BRITISH JOURNAL OF HAEMATOLOGY, 2021, 195 (01) : 95 - 107
  • [8] A Limited Plasma Cell Flow Cytometry Panel With Reflex CD138 Immunohistochemistry Is an Optimal Workflow Process for Evaluating Plasma Cell Neoplasms in Bone Marrow Specimens
    Chen, Zhongchuan Will
    Perkins, Sherrie L.
    Weiss, Ronald L.
    Bahler, David W.
    Hussong, Jerry W.
    Salama, Mohamed E.
    AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2015, 143 (01) : 78 - 83
  • [9] The success rate of interphase fluorescence in situ hybridization in plasma cell disorders can be improved using unconventional sources of plasma cells
    Panakkal, Vandana
    Rana, Sonia
    Rathore, Shailja
    Anshu, Anshu
    Balakrishnan, Anand
    Singh, Charanpreet
    Jandial, Aditya
    Sachdeva, Man Updesh Singh
    Varma, Neelam
    Lad, Deepesh
    Malhotra, Pankaj
    Sreedharanunni, Sreejesh
    INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, 2022, 44 (01) : 157 - 162
  • [10] Quantification of whole-cell in situ hybridization with oligonucleotide probes by flow cytometry of Escherichia coli cells
    Joachimsthal, EL
    Ivanov, V
    Tay, STL
    Tay, JH
    WORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY, 2003, 19 (05) : 527 - 533