Research Article

MYD88 L265P Mutations Are Correlated with 6q Deletion in Korean Patients with Waldenström Macroglobulinemia

Table 3

Patient characteristics and interphase FISH results according to the presence of MYD88 L265P mutation.

CharacteristicsMYD88 L265P (+)MYD88 L265P (−)

Age 65 years6/11 (55)2/5 (40)0.590
Male sex9/11 (82)3/5 (60)0.350
B symptoms7/11 (64)3/5 (60)0.889
Hyperviscosity5/11 (46)1/5 (20)0.330
Splenomegaly5/11 (46)2/5 (40)0.839
Lymphadenopathy7/11 (64)5/5 (100)0.120
Multiple osteolytic lesions1/11 (9)1/5 (20)0.541
Hemoglobin 11.5 g/dL10/11 (91)5/5 (100)0.486
Platelet 100 109/L2/11 (18)2/5 (40)0.350
Death2/11 (18)2/5 (40)0.350
IgM type monoclonal protein10/11 (91)3/5 (60)0.142
Monoclonal protein (g/dL)3.56 (0.50–5.43)2.94 (0.55–9.74)0.777
PB lymphocytes ( 106/L)2233 (807–6100)1415 (1067–21775)0.955
BM lymphocytes (%)45.0 (14.4–93.2)20.7 (3.0–84.7)0.234
BM plasma cells (%)3.7 (0–14.0)3.2 (0–32.9)0.691
BM cellularity (%)85 (25–95)60 (25–85)0.093
High lymphocyte burden in BM biopsy7/11 (64)0/5 (0)0.017
6q21 deletion6/11 (55)0/5 (0)0.037
IGH (14q32) translocation2/11 (18)2/5 (40)0.350
P53 (17p13) deletion1/11 (9)0/5 (0)0.486
1q25 amplification0/11 (0)1/5 (20)0.126
Abnormal karyotype3/7 (43)2/5 (40)0.921

BM: bone marrow; FISH: fluorescence in situ hybridization; Ig: immunoglobulin; PB: peripheral blood.
* P values were calculated using test for categorical variables and Mann-Whitney test for continuous variables between patients with or without the MYD88 L265P mutation.
BM cellularity ≥ 80% with diffuse lymphocytes infiltration in BM biopsy.