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Bendamustine plus rituximab for chronic cold agglutinin disease: results of a Nordic prospective multicenter trial.
Berentsen, Sigbjørn; Randen, Ulla; Oksman, Markku; Birgens, Henrik; Tvedt, Tor Henrik Anderson; Dalgaard, Jakob; Galteland, Eivind; Haukås, Einar; Brudevold, Robert; Sørbø, Jon Hjalmar; Næss, Inger Anne; Malecka, Agnieszka; Tjønnfjord, Geir E.
Afiliação
  • Berentsen S; Department of Research and Innovation, Haugesund Hospital, Haugesund, Norway.
  • Randen U; Department of Pathology, Oslo University Hospital, Oslo, Norway.
  • Oksman M; Department of Pathology, Akershus University Hospital, Lørenskog, Norway.
  • Birgens H; Department of Hematology and Stem Cell Transplantation, Division of Medicine, Turku University Hospital, Turku, Finland.
  • Tvedt THA; Department of Internal Medicine, Turku City Hospital, Turku, Finland.
  • Dalgaard J; Department of Haematology, Herlev Hospital, University of Copenhagen, Herlev, Denmark.
  • Galteland E; Department of Medicine, Haukeland University Hospital, Bergen, Norway.
  • Haukås E; Section for Hematology, Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Brudevold R; Medical Department, Drammen Hospital, Vestre Viken Trust, Drammen, Norway.
  • Sørbø JH; Department of Medicine, Akershus University Hospital, Lørenskog, Norway.
  • Næss IA; Department of Haematology, Oslo University Hospital, Oslo, Norway.
  • Malecka A; Department of Hematology and Oncology, Stavanger University Hospital, Stavanger, Norway.
  • Tjønnfjord GE; Department of Medicine, Ålesund Hospital, Ålesund, Norway.
Blood ; 130(4): 537-541, 2017 07 27.
Article em En | MEDLINE | ID: mdl-28533306
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Anemia Hemolítica Autoimune Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Anemia Hemolítica Autoimune Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article