This study examined the outcome of 248
Waldenstrom macroglobulinaemia (WM)
rituximab-naïve patients who responded to a
rituximab-containing regimen. Eighty-six patients (35%) subsequently received maintenance
rituximab (M-
Rituximab). No differences in baseline characteristics, and post-induction categorical responses between cohorts were observed. The median
rituximab infusions during induction was 6 for both cohorts; and 8 over a 2-year period for patients receiving M-
Rituximab. Categorical responses improved in 16/162 (10%) of observed, and 36/86 (41·8%) of M-
Rituximab patients respectively, following induction
therapy (P < 0·0001). Both progression-free (56·3 vs. 28·6 months; P = 0·0001) and overall survival (Not reached versus 116 months; P = 0·0095) were longer in patients who received M-
Rituximab. Improved progression-free survival was evident despite previous treatment status, induction with
rituximab alone or in combination
therapy (P ≤ 0·0001). Best serum
IgM response was lower (P < 0·0001), and haematocrit higher (P = 0·001) for patients receiving M-
Rituximab. Among patients receiving M-
Rituximab, an increased number of infectious events were observed, but were mainly ≤ grade 2 (P = 0·008). The findings of this observational study suggest improved clinical outcomes following M-
Rituximab in WM patients who respond to induction with a
rituximab-containing regimen. Prospective studies aimed at clarifying the role of M-
Rituximab therapy in WM patients are needed to confirm these findings.