The immunophenotypic stability of plasma cell myeloma by flow cytometry

被引:15
作者
Spears, M. D. [1 ]
Olteanu, H. [1 ]
Kroft, S. H. [1 ]
Harrington, A. M. [1 ]
机构
[1] Med Coll Wisconsin, Dept Pathol, Milwaukee, WI 53226 USA
关键词
Plasma cell myeloma; flow cytometry; minimal residual disease; immunophenotype; stability; MULTIPLE-MYELOMA; PROGNOSTIC-FACTOR; EXPRESSION; LEUKEMIA; APPLICABILITY; BANDS;
D O I
10.1111/j.1751-553X.2011.01317.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Flow cytometry (FC) has become increasingly utilized in the diagnosis and monitoring of plasma cell myeloma (PCM), though few studies have evaluated the longitudinal stability of antigen expression. Methods: We studied 45 PCM patients by four-color FC for shifts in CD19, CD20, CD38, CD45, CD56, and cytoplasmic light chain expression, between diagnostic/first encounter and positive follow-up analyses. An immunophenotypic (IP) change was defined as gain, loss, or 1/2 log shift of antigen expression. Results: An IP change was observed in 14/45 (31%) patients, with single IP changes in 9/14, two changes in 2/14, and three changes in 3/14. 3/14 reverted from an aberrant to a normal plasma cell IP, while remaining light chain-restricted. Changes in expression of CD45 occurred in 9/45 (20%), CD19 in 5/45 (11.1%), CD20 in 2/45 (4.4%), and CD56 in 5/45 (11.1%). Conclusion: Approximately 1/3 of PCM cases show IP changes over time, with CD45 the least stable antigen. Recognition of this relative instability is important to avoid narrow targeting of follow-up FC analyses, especially for minimal residual disease monitoring.
引用
收藏
页码:483 / 491
页数:9
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