Cold agglutinin disease revisited: a multinational, observational study of 232 patients

Sigbjørn Berentsen(Privatsykehuset Haugesund), Wilma Barcellini(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Shirley D’Sa(University College London Hospitals NHS Foundation Trust), Ulla Randen(Akershus University Hospital), Tor Henrik Anderson Tvedt(Haukeland University Hospital), Bruno Fattizzo(University of Milan), Einar Haukås(Stavanger University Hospital), Megan Kell(University College London Hospitals NHS Foundation Trust), Robert Brudevold(Ålesund Hospital), Anders Erik Astrup Dahm(University of Oslo), Jakob Dalgaard(Drammen Hospital), Hege Frøen(Vestre Viken Hospital Trust), Randi Fykse Hallstensen(Nordland Hospital), Pernille H. Jæger(St Olav's University Hospital), Henrik Hjorth‐Hansen(Norwegian University of Science and Technology), Agnieszka Małecka(Oslo University Hospital), Markku Oksman(Turku University Hospital), Jürgen Rolke(Sørlandet Sykehus), Mallika Sekhar(Royal Free London NHS Foundation Trust), Jon Hjalmar Sørbø(Levanger Hospital), Eirik Tjønnfjord(Østfold Hospital Trust), Galina Tsykunova(Haukeland University Hospital), Geir E. Tjønnfjord(University of Oslo)
Blood
May 7, 2020
Cited by 165Open Access
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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.


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