TY - JOUR
T1 - Clinical presentation, progression, and outcome of patients with Clonal B-cell counts of less than 5 × 109/L, 5 to 10 × 109/L, and more than 10 × 109/L and chronic lymphocytic leukemia immunophenotype
AU - Foster, Angela E.
AU - Nguyen, Tu Dung T.
AU - Al-Hammadi, Noor
AU - Frater, John L.
AU - Hassan, Anjum
AU - Kreisel, Friederike
N1 - Publisher Copyright:
© 2015 American Society for Clinical Pathology.
PY - 2015/1
Y1 - 2015/1
N2 - Objectives: The flow cytometric evaluation of peripheral lymphocytosis has led to a dramatic increase in the diagnosis of early stage chronic lymphocytic leukemia (CLL) and monoclonal B-cell lymphocytosis (MBL). Few studies exist to better delineate the natural history and differences between MBL and CLL. Methods: Applying the recently updated B-lymphocyte threshold of 5 × 109 B lymphocytes/L for the diagnosis of CLL, we evaluated the differences in initial presentation, disease progression, time to treatment (TTT), and 10-year overall survival rates between patients with less than 5 × 10 × 109/L, 5 to 10 × 109/L, and more than 10 × 109/L B cells. These clinical/treatment parameters were also compared among the MBL, 5 to 10 CLL Rai stage 0, and more than 10 CLL Rai stage 0 groups. Results: In total, 310 patients were included, with 67 in the less than 5, 75 in the 5 to 10, and 168 in the more than 10 B-cell groups. Statistically significant differences were seen when comparing the 5 to 10 and more than 10 B-cell groups regarding anemia (P = .021 for median hemoglobin; P = .028 for anemia <11 g/dL), platelet count (P = .041 for median platelet count), splenomegaly (P = .013), initial management plan (P = .012 for observation; P = .0021 for treatment with chemotherapy), and TTT (P = .0033). No statistically significant difference was seen among the MBL, 5 to 10, and more than 10 CLL Rai stage 0 groups regarding TTT and 10-year overall survival. Conclusions: Findings suggest that patients with B-cell counts of 5 to 10 × 109/L behave clinically more similar to patients with B-cell counts of less than 5 × 109/L.
AB - Objectives: The flow cytometric evaluation of peripheral lymphocytosis has led to a dramatic increase in the diagnosis of early stage chronic lymphocytic leukemia (CLL) and monoclonal B-cell lymphocytosis (MBL). Few studies exist to better delineate the natural history and differences between MBL and CLL. Methods: Applying the recently updated B-lymphocyte threshold of 5 × 109 B lymphocytes/L for the diagnosis of CLL, we evaluated the differences in initial presentation, disease progression, time to treatment (TTT), and 10-year overall survival rates between patients with less than 5 × 10 × 109/L, 5 to 10 × 109/L, and more than 10 × 109/L B cells. These clinical/treatment parameters were also compared among the MBL, 5 to 10 CLL Rai stage 0, and more than 10 CLL Rai stage 0 groups. Results: In total, 310 patients were included, with 67 in the less than 5, 75 in the 5 to 10, and 168 in the more than 10 B-cell groups. Statistically significant differences were seen when comparing the 5 to 10 and more than 10 B-cell groups regarding anemia (P = .021 for median hemoglobin; P = .028 for anemia <11 g/dL), platelet count (P = .041 for median platelet count), splenomegaly (P = .013), initial management plan (P = .012 for observation; P = .0021 for treatment with chemotherapy), and TTT (P = .0033). No statistically significant difference was seen among the MBL, 5 to 10, and more than 10 CLL Rai stage 0 groups regarding TTT and 10-year overall survival. Conclusions: Findings suggest that patients with B-cell counts of 5 to 10 × 109/L behave clinically more similar to patients with B-cell counts of less than 5 × 109/L.
KW - 10-year survival rate
KW - CLL
KW - Monoclonal B-cell lymphocytosis
KW - Time to treatment
UR - http://www.scopus.com/inward/record.url?scp=84923541667&partnerID=8YFLogxK
U2 - 10.1309/AJCPIXUB5MZK8ECI
DO - 10.1309/AJCPIXUB5MZK8ECI
M3 - Article
C2 - 25511144
AN - SCOPUS:84923541667
SN - 0002-9173
VL - 143
SP - 70
EP - 77
JO - American journal of clinical pathology
JF - American journal of clinical pathology
IS - 1
ER -