| Literature DB >> 25263319 |
Elisabet E Manasanch1, Dalia A Salem, Constance M Yuan, Nishant Tageja, Manisha Bhutani, Mary Kwok, Dickran Kazandjian, George Carter, Seth M Steinberg, Diamond Zuchlinski, Marcia Mulquin, Katherine Calvo, Irina Maric, Mark Roschewski, Neha Korde, Raul Braylan, Ola Landgren, Maryalice Stetler-Stevenson.
Abstract
Flow cytometry has increasing relevance for prognosis in myeloma and precursor disease (monoclonal gammopathy of unknown significance/smoldering myeloma), yet it has been reported that plasma cell enumeration by flow varies depending on the quality of marrow aspirate and field biopsied in patchy disease. We demonstrated increased sensitivity of flow over immunohistochemistry in abnormal-plasma cell detection in monoclonal gammopathy (n = 59)/smoldering myeloma (n = 87). We prospectively evaluated treatment-na ve smoldering myeloma (n = 9)/myeloma (n = 11) patients for the percentage of abnormal plasma cells/total plasma cell compartment, plasma cell viability/infiltration and flow immunophenotype depending on anticoagulant use, biopsy site and pull sequence in uni-and-bilateral bone marrow biopsies and aspirates. We found no statistical difference regarding the percentage of abnormal plasma cells, their immunophenotype or number/distribution in marrow samples even when obtained by different sequence in aspirates, or anticoagulants (p > 0.05). Our results show that plasma cell enumeration and immunophenotyping by flow cytometry is consistent under different conditions in these populations.Entities:
Keywords: Smoldering; enumeration; flow; myeloma; plasma cell; risk
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Year: 2014 PMID: 25263319 PMCID: PMC5576181 DOI: 10.3109/10428194.2014.955020
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022