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. Author manuscript; available in PMC: 2017 Apr 28.
Published in final edited form as: Br J Haematol. 2015 Dec 13;172(5):735–744. doi: 10.1111/bjh.13897

Table I.

Baseline characteristics for WM and IgM MGUS patients whose samples were evaluated for CXCR4 mutations by AS-PCR and Sanger sequencing.

Untreated WM Previously Treated WM IgM MGUS
N 102 62 12
Age (years) 62 (33–88) 63 (44–86) 69 (56–82)
Gender (Male/Female) 58/44 48/15 6/6
Serum IgM (g/l) 26·70 (2·70–86·30) 36·10 (7·35–83·90) 3·97 (1·42–16·40)
Haemoglobin (g/l) 117 (48–155) 105 (82–138) 134 (119–163)
Serum β2-microglobulin (mg/l) 2·9 (1·0–9·5) 3·9 (1·3–14·2) 1·9 (1·7–3·4)
Adenopathy ( 1·5 cm) 34 (33·3%) 37 (58·7%) 0 (0%)
Splenomegaly (≥15 cm) 15 (14·7%) 7 (11·1%) 0 (0%)
Bone marrow involvement (%) by IHC 40 (5–95) 60 (3–95) 0 (0%) (0–0)
MYD88L265P positive 97 (95·1%) 55 (89%) 6 (50%)

WM, Waldenström Macroglobulinaemia; IgM, immunoglobulin M; MGUS, monoclonal gammopathy of unknown significance; AS-PCR, allele-specific polymerase chain reaction; IHC, immunohistochemistry.

Values are shown as median (range) unless otherwise indicated.