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Cold agglutinin disease revisited: a multinational, observational study of 232 patients.
Berentsen, Sigbjørn; Barcellini, Wilma; D'Sa, Shirley; Randen, Ulla; Tvedt, Tor Henrik Anderson; Fattizzo, Bruno; Haukås, Einar; Kell, Megan; Brudevold, Robert; Dahm, Anders E A; Dalgaard, Jakob; Frøen, Hege; Hallstensen, Randi Fykse; Jæger, Pernille H; Hjorth-Hansen, Henrik; Malecka, Agnieszka; Oksman, Markku; Rolke, Jürgen; Sekhar, Mallika; Sørbø, Jon Hjalmar; Tjønnfjord, Eirik; Tsykunova, Galina; Tjønnfjord, Geir E.
Afiliação
  • Berentsen S; Department of Research and Innovation, Haugesund Hospital, Helse Fonna Hospital Trust, Haugesund, Norway.
  • Barcellini W; Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
  • D'Sa S; Cancer Division, University College London Hospitals NHS Foundation Trust, London, United Kingdom.
  • Randen U; Department of Pathology, Akershus University Hospital, Lørenskog, Norway.
  • Tvedt THA; Department of Medicine, Haukeland University Hospital, Bergen, Norway.
  • Fattizzo B; Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
  • Haukås E; Department of Oncology and Onco-Hematology, University of Milan, Milan, Italy.
  • Kell M; Department of Blood and Cancer Diseases, Stavanger University Hospital, Stavanger, Norway.
  • Brudevold R; Cancer Division, University College London Hospitals NHS Foundation Trust, London, United Kingdom.
  • Dahm AEA; Department of Medicine, Ålesund Hospital, Helse Møre og Romsdal Hopspital Trust, Ålesund, Norway.
  • Dalgaard J; Department of Haematology, Akershus University Hospital, Lørenskog, Norway.
  • Frøen H; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
  • Hallstensen RF; Department of Medicine, Drammen Hospital, Vestre Viken Hospital Trust, Drammen, Norway.
  • Jæger PH; Department of Medicine, Bærum Hospital, Vestre Viken Hospital Trust, Gjettum, Norway.
  • Hjorth-Hansen H; Department of Medicine, Nordland Hospital, Bodø, Norway.
  • Malecka A; Department of Hematology, St Olav University Hospital, Trondheim, Norway.
  • Oksman M; Faculty of Medicine and Health Sciences and.
  • Rolke J; Department of Hematology, St Olav University Hospital, Trondheim, Norway.
  • Sekhar M; Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
  • Sørbø JH; Department of Haematology and.
  • Tjønnfjord E; Department of Pathology, Oslo University Hospital, Oslo, Norway.
  • Tsykunova G; KG Jebsen Centre for B-cell Malignancies, Institute of Clinical Medicine, University of Oslo, Oslo Norway.
  • Tjønnfjord GE; Department of Internal Medicine, Turku City Hospital, Turku, Finland.
Blood ; 136(4): 480-488, 2020 07 23.
Article em En | MEDLINE | ID: mdl-32374875
ABSTRACT
We retrospectively studied 232 patients with cold agglutinin disease (CAD) at 24 centers in 5 countries. In Norway and a northern region of Italy, the study was close to being population-based. For the first time, we demonstrate fourfold differences between cold and warmer climates regarding prevalence (20 vs 5 cases/million) and incidence (1.9 vs 0.48 cases/million per year). Mean baseline hemoglobin level was 9.3 g/dL, but 27% had hemoglobin <8 g/dL. Identification of typical features of CAD-associated lymphoproliferative disorder in the bone marrow was greatly increased by centralized biopsy assessment. CAD seems to be associated with a slightly increased risk of venous thrombosis. This work includes a follow-up study of therapies, focusing on the long-term outcomes of the rituximab plus bendamustine and rituximab plus fludarabine regimens. Rituximab plus bendamustine therapy resulted in responses in 35 (78%) of 45 patients; 24 (53%) achieved complete response. Interestingly, these rates were still higher than observed in the original (2017) prospective trial, and we also found a shift toward deeper responses with time. This is explained by the prolonged time to response seen in many patients, probably related to long-lived plasma cells. In patients responding to rituximab-bendamustine, median response duration was not reached after 88 months, and estimated 5-year sustained remission was 77%. The regimen appeared safe regarding late-occurring malignancies. Rituximab plus fludarabine therapy seems to carry a higher risk of long-term adverse effects.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vidarabina / Cloridrato de Bendamustina / Rituximab / Anemia Hemolítica Autoimune Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vidarabina / Cloridrato de Bendamustina / Rituximab / Anemia Hemolítica Autoimune Idioma: En Ano de publicação: 2020 Tipo de documento: Article