| Literature DB >> 32374875 |
Sigbjørn Berentsen1, Wilma Barcellini2, Shirley D'Sa3, Ulla Randen4, Tor Henrik Anderson Tvedt5, Bruno Fattizzo2,6, Einar Haukås7, Megan Kell3, Robert Brudevold8, Anders E A Dahm9,10, Jakob Dalgaard11, Hege Frøen12, Randi Fykse Hallstensen13, Pernille H Jæger14,15, Henrik Hjorth-Hansen14,16, Agnieszka Małecka17,18,19, Markku Oksman20,21, Jürgen Rolke22, Mallika Sekhar23, Jon Hjalmar Sørbø24, Eirik Tjønnfjord25, Galina Tsykunova5, Geir E Tjønnfjord17,19.
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.Entities:
Year: 2020 PMID: 32374875 DOI: 10.1182/blood.2020005674
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113