| Literature DB >> 28383205 |
Jorge J Castillo1, Artur Jurczyszyn2, Lucie Brozova3, Edvan Crusoe4, Jacek Czepiel2, Julio Davila5, Angela Dispenzieri6, Marion Eveillard7, Mark A Fiala8, Irene M Ghobrial1, Alessandro Gozzetti9, Joshua N Gustine1, Roman Hajek10, Vania Hungria11, Jiri Jarkovsky3, David Jayabalan12, Jacob P Laubach1, Barbara Lewicka2, Vladimir Maisnar13, Elisabet E Manasanch14, Philippe Moreau6, Elizabeth A Morgan1, Hareth Nahi15, Ruben Niesvizky12, Claudia Paba-Prada1, Tomas Pika16, Ludek Pour17, John L Reagan18, Paul G Richardson1, Jatin Shah14, Ivan Spicka19, Ravi Vij8, Anna Waszczuk-Gajda20, Morie A Gertz6.
Abstract
IgM myeloma is a rare hematologic malignancy for which the clinicopathological features and patient outcomes have not been extensively studied. We carried out a multicenter retrospective study in patients with diagnosis of IgM myeloma defined by >10% marrow involvement by monoclonal plasma cells, presence of an IgM monoclonal paraproteinemia of any size, and anemia, renal dysfunction, hypercalcemia, lytic lesions and/or t(11;14) identified by FISH. A total of 134 patients from 20 centers were included in this analysis. The median age at diagnosis was 65.5 years with a male predominance (68%). Anemia, renal dysfunction, elevated calcium and skeletal lytic lesions were found in 37, 43, 19, and 70%, respectively. The median serum IgM level was 2,895 mg dL-1 with 19% of patients presenting with levels >6,000 mg dL-1 . International Staging System (ISS) stages 1, 2, and 3 were seen in 40 (33%), 54 (44%), and 29 (24%) of patients, respectively. The malignant cells expressed CD20 (58%) and cyclin D1 (67%), and t(11;14) was the most common cytogenetic finding (39%). The median overall survival (OS) was 61 months. Higher ISS score was associated with worse survival (P = 0.02). Patients with IgM myeloma present with similar characteristics and outcomes as patients with more common myeloma subtypes.Entities:
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Year: 2017 PMID: 28383205 DOI: 10.1002/ajh.24753
Source DB: PubMed Journal: Am J Hematol ISSN: 0361-8609 Impact factor: 10.047