| Literature DB >> 28533306 |
Sigbjørn Berentsen1, Ulla Randen2,3, Markku Oksman4,5, Henrik Birgens6, Tor Henrik Anderson Tvedt7,8, Jakob Dalgaard9, Eivind Galteland10,11, Einar Haukås12, Robert Brudevold13, Jon Hjalmar Sørbø14, Inger Anne Næss15, Agnieszka Malecka2,16, Geir E Tjønnfjord11,17.
Abstract
Primary chronic cold agglutinin disease (CAD) is a well-defined clinicopathologic entity in which a bone marrow clonal B-cell lymphoproliferation results in autoimmune hemolytic anemia and cold-induced circulatory symptoms. Rituximab monotherapy and fludarabine-rituximab in combination are documented treatment options. In a prospective, nonrandomized multicenter trial, 45 eligible patients received rituximab 375 mg/m2 day 1 and bendamustine 90 mg/m2 days 1 and 2 for 4 cycles at a 28-day interval. Thirty-two patients (71%) responded; 18 (40%) achieved complete response (CR) and 14 (31%) partial response (PR). Among 14 patients previously treated with rituximab or fludarabine-rituximab, 7 (50%) responded to bendamustine-rituximab (3 CR and 4 PR). Hemoglobin levels increased by a median of 4.4 g/dL in the complete responders, 3.9 g/dL in those achieving PR, and 3.7 g/dL in the whole cohort. The 10th percentile of response duration was not reached after 32 months. Grade 3-4 neutropenia occurred in 15 patients (33%), but only 5 (11%) experienced infection with or without neutropenia. Thirteen patients (29%) had their dose of bendamustine reduced. In conclusion, bendamustine-rituximab combination therapy is highly efficient, sufficiently safe, and may be considered in first line for patients with CAD requiring therapy. The trial was registered at www.clinicaltrials.gov as #NCT02689986.Entities:
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Year: 2017 PMID: 28533306 DOI: 10.1182/blood-2017-04-778175
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113