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Low-count monoclonal B-cell lymphocytosis persists after seven years of follow up and is associated with a poorer outcome.
- Source :
-
Haematologica [Haematologica] 2018 Jul; Vol. 103 (7), pp. 1198-1208. Date of Electronic Publication: 2018 Mar 22. - Publication Year :
- 2018
-
Abstract
- Low-count monoclonal B-cell lymphocytosis is defined by the presence of very low numbers of circulating clonal B cells, usually phenotypically similar to chronic lymphocytic leukemia cells, whose biological and clinical significance remains elusive. Herein, we re-evaluated 65/91 low-count monoclonal B-cell lymphocytosis cases (54 chronic lymphocytic leukemia-like and 11 non-chronic lymphocytic leukemia-like) followed-up for a median of seven years, using high-sensitivity flow cytometry and interphase fluorescence in situ hybridization. Overall, the clone size significantly increased in 69% of low-count monoclonal B-cell lymphocytosis cases, but only one subject progressed to high-count monoclonal B-cell lymphocytosis. In parallel, the frequency of cytogenetic alterations increased over time (32% vs 61% of cases, respectively). The absolute number of the major T-cell and natural killer cell populations also increased, but only among chronic lymphocytic leukemia-like cases with increased clone size vs age- and sex-matched controls. Although progression to chronic lymphocytic leukemia was not observed, the overall survival of low-count monoclonal B-cell lymphocytosis individuals was significantly reduced vs non-monoclonal B-cell lymphocytosis controls ( P =0.03) plus the general population from the same region ( P ≤0.001), particularly among females ( P =0.01); infection and cancer were the main causes of death in low-count monoclonal B-cell lymphocytosis. In summary, despite the fact that mid-term progression from low-count monoclonal B-cell lymphocytosis to high-count monoclonal B-cell lymphocytosis and chronic lymphocytic leukemia appears to be unlikely, these clones persist at increased numbers, usually carrying more genetic alterations, and might thus be a marker of an impaired immune system indirectly associated with a poorer outcome, particularly among females.<br /> (Copyright© 2018 Ferrata Storti Foundation.)
- Subjects :
- Adult
Aged
Aged, 80 and over
B-Lymphocytes metabolism
Biomarkers
Chromosome Aberrations
Disease Progression
Female
Flow Cytometry
Follow-Up Studies
Humans
Immunophenotyping
Killer Cells, Natural immunology
Killer Cells, Natural metabolism
Lymphocytosis genetics
Lymphocytosis mortality
Male
Middle Aged
Prognosis
T-Lymphocytes immunology
T-Lymphocytes metabolism
Time Factors
B-Lymphocytes pathology
Clonal Evolution
Lymphocyte Count
Lymphocytosis blood
Lymphocytosis pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1592-8721
- Volume :
- 103
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Haematologica
- Publication Type :
- Academic Journal
- Accession number :
- 29567775
- Full Text :
- https://doi.org/10.3324/haematol.2017.183954