Clinical characteristic and outcome of lymphoplasmacytic lymphoma of non‐Waldenstrom macroglobulinemia type: A Swedish lymphoma registry study

Summary Lymphoplasmacytic lymphoma (LPL) not fulfilling the WHO diagnostic criteria (2017) for Waldenstrom’s macroglobulinemia (WM) (named non‐WM LPL) is a rare disease and only a few systematic studies have been published. Here, we present a population‐based study of non‐WM LPL focusing on diagnost...

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Veröffentlicht in:British journal of haematology Jg. 196; H. 6; S. 1362 - 1368
Hauptverfasser: Brandefors, Lena, Sander, Birgitta, Lundqvist, Kristina, Kimby, Eva
Format: Journal Article
Sprache:Englisch
Veröffentlicht: England Blackwell Publishing Ltd 01.03.2022
Schlagworte:
clinical aspects
Diagnosis
epidemiology
Hematology
Humans
Immunoglobulin A
Immunoglobulin G
Lymphocytosis
Lymphoma
Lymphoma, B-Cell
lymphoplasmacytic lymphoma
Macroglobulinemia
Medical prognosis
Medical treatment
Patients
Population studies
Rare diseases
Registries
risk factors
Survival
Sweden - epidemiology
Waldenstrom Macroglobulinemia - drug therapy
Sweden
epidemiology
clinical aspects
risk factors
lymphoplasmacytic lymphoma
ISSN:0007-1048, 1365-2141, 1365-2141
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Zusammenfassung:Summary Lymphoplasmacytic lymphoma (LPL) not fulfilling the WHO diagnostic criteria (2017) for Waldenstrom’s macroglobulinemia (WM) (named non‐WM LPL) is a rare disease and only a few systematic studies have been published. Here, we present a population‐based study of non‐WM LPL focusing on diagnostic difficulties, patient characteristics, and outcome. From 1511 patients included in the Swedish Lymphoma Registry 1 Jan 2000 – 31 Dec 2014 with a diagnosis of WM/LPL, we could confirm the diagnosis of non‐WM LP in only 33 patients. The median age at diagnosis was 69 years. A paraprotein was found in most (IgG in 54%, IgA in 15%) and 12% of the cases were non‐secretory. Compared with the WM patients, the non‐WM LPL patients were younger, had more adverse prognostic factors such as elevated LDH, anaemia, and lymphocytosis at diagnosis. In addition, the non‐WM LPL patients more often were symptomatic and received treatment at diagnosis. The overall survival (OS) did not significantly differ between the non‐WM LPL and WM groups (P = 0.247), with a median survival time of 71 and 96 months, respectively. To conclude, we found differences in clinical features between WM and non‐WM LPL, but no difference in survival.
Bibliographie:ObjectType-Article-1
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ISSN:0007-1048
1365-2141
1365-2141
DOI:10.1111/bjh.18002