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Original Articles

Intensity of antigen expression reflects IGHV mutational status and Dohner-defined prognostic categories in chronic lymphocytic leukemia, monoclonal B-cell lymphocytosis, and small lymphocytic lymphoma

ORCID Icon, , , , ORCID Icon, , , , , ORCID Icon & ORCID Icon show all
Pages 1828-1839 | Received 09 Apr 2020, Accepted 14 Feb 2021, Published online: 18 Mar 2021
 

Abstract

We demonstrate the prognostic utility of antigen quantitation in chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) and monoclonal B-cell lymphocytosis (MBL). Median antibody-bound-per-cell (ABC) of CD20, CD22, CD25, CD19, and %CD38(+) was determined in CLL (185/208), SLL (8/208) and MBL (15/208) cases by flow cytometry, then compared to Dohner-classification, immunoglobulin status (mutated, IGHV-M; unmutated, IGHV-U), CLL-IPI risk and time to first treatment (TTFT). Trisomy 12 cases showed increased %CD38-expression (p = .0379). Higher %CD38 was observed in IGHV-U versus IGHV-M (p = .0003). CD20ABC was increased in IGHV-U versus IGHV-M (p = .006). Del13q cases demonstrated lower CD22ABC (p = .0198). Cases without cytogenetic abnormality exhibited higher CD19ABC (p = .0295) and CD22ABC (p = .0078). Del17p cases demonstrated lower CD25ABC (p = .0097). High and very-high CLL-IPI risk groups were associated with high CD38-expression (p = .02) and low CD25ABC (p = .0004). Shortened TTFT was associated with high CD38-expression (p < .0001). Interestingly, high CD25ABC trended toward shortened TTFT (p = .07). Quantitative antigen expression reflects CLL-IPI risk groups and Dohner-classification.

Acknowledgements

We gratefully thank Dr. Diane Arthur for her cytogenetics expertise.

This work is dedicated in loving memory of Gregory Jasper, whose decades of dedication made it possible.

Disclosure statement

The author(s) have no conflicts of interest or funding to disclose.

Disclaimer

The authors are responsible for the results and views expressed in this manuscript.

Additional information

Funding

This study was supported by funding from the intramural program of the Center for Cancer Research, National Cancer Institute, and the National Heart, Lung, and Blood Institute, National Institutes of Health.

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