Extramedullary disease in Waldenström macroglobulinemia: A population‐based observational study
Year: 2024
Type: article
Study design: Observational Study
Abstract: INTRODUCTION: Extramedullary disease (EMD) is a rare manifestation of Waldenström macroglobulinemia (WM), and its clinical and prognostic implications are poorly understood. METHODS: In this single-center study, we investigated the clinical significance of EMD in a cohort of 469 WM patients. RESULTS: EMD was identified in 30 (6.4%) patients, with the central nervous system, kidneys, and lungs being the most frequently affected sites. The cumulative incidence of EMD was 12.6% at 15 years. Median overall survival rates at 5 and 10 years for patients with EMD were 63% and 37%, respectively. CONCLUSION: Our findings indicate a persistent risk of EMD throughout the disease course, with no significant impact on long-term survival.
Source: eJHaem
DOI: 10.1002/jha2.1037
Language: English
Subfield: Genetics
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,600
Funder: Region Sjælland
Award: G3307809233
OpenAlex ID: W4403770106
