@article {8030,
	title = {Treatment of Waldenstrom{\textquoteright}s macroglobulinemia with rituximab: Prognostic factors for response and progression},
	journal = {Leukemia and Lymphoma},
	volume = {45},
	year = {2004},
	note = {Cited By :29Export Date: 21 February 2017},
	month = {2004},
	pages = {2057 - 2061},
	abstract = {Recent data have suggested that rituximab is an active agent for the treatment of Waldenstrom{\textquoteright}s macroglobulinemia (WM). However, the patients that are more likely to benefit have not been clearly defined. In order to address this question we evaluated 52 patients who were treated with single-agent rituximab in the context of prospective studies. Several clinical and laboratory variables were assessed for their correlation with response and time to progression. Twenty-three (44\%) patients achieved a partial response after treatment with rituximab. Previously untreated and pretreated patients had the same probability for response. Higher response rates were noted in patients with serum monoclonal protein < 40 g/l, with serum albumin >= 35 g/l and with kappa light chain. The median time to progression for all patients was 13.8 months. A multivariate analysis indicated that elevated serum monoclonal protein levels and low serum albumin were the dominant variables associated with shorter progression. Presence of two, one or none of these adverse prognostic factors was associated with time to progression of 3.6 months, 11 months and more than 40 months, respectively. We conclude that rituximab is an effective treatment modality for patients with WM. Patients with both low levels of monoclonal protein and normal albumin are the best candidates for treatment with standard dose rituximab. {\textcopyright} 2004 Taylor \& Francis Ltd.},
	keywords = {rituximab, Waldenstr{\"o}m{\textquoteright}s macroglobulinemia},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-4544309544\&doi=10.1080\%2f10428190410001723287\&partnerID=40\&md5=7d34c630d14f0bf2fe8990a96cd19ac3},
	author = {Dimopoulos A., M.A. and Alexanian, R. and Gika, D. and Anagnostopoulos, A. and Zervas, C. and Zomas, A. and Kyrtsonis, M.C. and Anagnostopoulos, N. and Pangalis, G.A. and Weber, D.M.}
}
