| Literature DB >> 31044423 |
Marcus Geer1, Emily Roberts1, Maryann Shango2, Brian G Till3, Stephen D Smith4, Hashim Abbas5, Brian T Hill6, Jason Kaplan7, Paul M Barr8, Paolo Caimi9, Deborah M Stephens10, Emily Lin11, Alex F Herrera12, Evan Rosenbaum13, Jennifer E Amengual14, Philip S Boonstra1, Sumana Devata15, Ryan A Wilcox15, Mark S Kaminski15, Tycel J Phillips15.
Abstract
Intravascular large B-cell lymphoma (IVLBCL) is a rare entity, with a generally aggressive course that may vary based on geographic presentation. While a United States (US) registry study showed relatively good outcomes with IVLBCL, clinicopathological and treatment data were unavailable. We performed a detailed retrospective review of cases identified at 8 US medical centres, to improve understanding of IVLBCL and inform management. We compiled data retrieved via an Institutional Review Board-approved review of IVLBCL cases identified from 1999 to 2015 at nine academic institutions across the US. We characterized the cohort's clinical status at time of diagnosis, presenting diagnostic and clinical features of the disease, treatment modalities used and overall prognostic data. Our cohort consisted of 54 patients with varying degrees of clinical features. Adjusting for age, better performance status at presentation was associated with increased survival time for the patients diagnosed in vivo (hazard ratio: 2·12, 95% confidence interval 1·28, 3·53). Based on the data we have collected, it would appear that the time interval to diagnosis is a significant contributor to outcomes of patients with IVLBCL.Entities:
Keywords: B cells; diagnostic haematology; lymphomas
Mesh:
Year: 2019 PMID: 31044423 PMCID: PMC8989046 DOI: 10.1111/bjh.15923
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998