| Literature DB >> 31992103 |
Jorge J Castillo1,2, Gilad Itchaki1,3, Joshua N Gustine1,4, Kirsten Meid1, Catherine A Flynn1, Maria G Demos1, Maria L Guerrera1, Cristina Jimenez1, Amanda Kofides1, Xia Liu1, Manit Munshi1, Nicholas Tsakmaklis1, Christopher J Patterson1, Lian Xu1, Guang Yang1, Zachary R Hunter1, Steven P Treon1,2.
Abstract
Cases of non-IgM lymphoplasmacytic lymphoma (LPL) are rare. We performed a case-control study comparing features and outcomes of 31 non-IgM LPL cases and 93 Waldenström macroglobulinemia (WM) controls matched by age, sex, and year of diagnosis. Odds of MYD88 mutations were lower (odds ratio (OR) 0.22, p = .05), and median time to treatment was shorter in cases than in controls (4 vs. 32 months; p < .001). Odds of extramedullary disease were higher (OR 4.20, p = .01), while odds of neuropathy (OR 0.22, p = .25), and hyperviscosity (OR 0.26, p = .26) were lower in cases than in controls. Odds of using chemoimmunotherapy were higher (OR 2.62, p = .11) while odds of using proteasome inhibitors (OR 0.35, p = .15) and BTK inhibitors (OR 0.17, p = .21) were lower in cases than in controls. There were no differences in response and overall survival (OS) between cases and controls. Despite clinicopathological differences, response, and survival outcomes are similar between non-IgM LPL cases and WM controls.Entities:
Keywords: Waldenstrom’s macroglobulinaemia; case–control study; lymphoplasmacytic lymphoma; response; survival
Mesh:
Year: 2020 PMID: 31992103 DOI: 10.1080/10428194.2020.1719100
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022