Conditional relative survival in Waldenström’s macroglobulinaemia: a population‐based study in The Netherlands

Contemporary diagnosed WM patients, compared to the general population, continue to experience excess mortality regardless of having survived up to 15 years post‐diagnosis. This gradual increase in excess mortality might result from the incurable nature of this disease characterized by multiple rela...

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Autores principales: Amaador, Karima, Kersten, Marie José, Visser, Otto, Posthuma, Eduardus F. M., Minnema, Monique C., Vos, Josephine M. I., Dinmohamed, Avinash G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Haematological malignancy–Clinical
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9297939/
https://www.ncbi.nlm.nih.gov/pubmed/34738239
http://dx.doi.org/10.1111/bjh.17926
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author Amaador, Karima
Kersten, Marie José
Visser, Otto
Posthuma, Eduardus F. M.
Minnema, Monique C.
Vos, Josephine M. I.
Dinmohamed, Avinash G.
author_facet Amaador, Karima
Kersten, Marie José
Visser, Otto
Posthuma, Eduardus F. M.
Minnema, Monique C.
Vos, Josephine M. I.
Dinmohamed, Avinash G.
author_sort Amaador, Karima
collection PubMed
description Contemporary diagnosed WM patients, compared to the general population, continue to experience excess mortality regardless of having survived up to 15 years post‐diagnosis. This gradual increase in excess mortality might result from the incurable nature of this disease characterized by multiple relapses throughout the disease course with limited efficacious treatment options in the released/refractory setting.
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spelling pubmed-92979392022-07-21 Conditional relative survival in Waldenström’s macroglobulinaemia: a population‐based study in The Netherlands Amaador, Karima Kersten, Marie José Visser, Otto Posthuma, Eduardus F. M. Minnema, Monique C. Vos, Josephine M. I. Dinmohamed, Avinash G. Br J Haematol Haematological malignancy–Clinical Contemporary diagnosed WM patients, compared to the general population, continue to experience excess mortality regardless of having survived up to 15 years post‐diagnosis. This gradual increase in excess mortality might result from the incurable nature of this disease characterized by multiple relapses throughout the disease course with limited efficacious treatment options in the released/refractory setting. John Wiley and Sons Inc. 2021-11-04 2022-03 /pmc/articles/PMC9297939/ /pubmed/34738239 http://dx.doi.org/10.1111/bjh.17926 Text en © 2021 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Haematological malignancy–Clinical
Amaador, Karima
Kersten, Marie José
Visser, Otto
Posthuma, Eduardus F. M.
Minnema, Monique C.
Vos, Josephine M. I.
Dinmohamed, Avinash G.
Conditional relative survival in Waldenström’s macroglobulinaemia: a population‐based study in The Netherlands
title Conditional relative survival in Waldenström’s macroglobulinaemia: a population‐based study in The Netherlands
title_full Conditional relative survival in Waldenström’s macroglobulinaemia: a population‐based study in The Netherlands
title_fullStr Conditional relative survival in Waldenström’s macroglobulinaemia: a population‐based study in The Netherlands
title_full_unstemmed Conditional relative survival in Waldenström’s macroglobulinaemia: a population‐based study in The Netherlands
title_short Conditional relative survival in Waldenström’s macroglobulinaemia: a population‐based study in The Netherlands
title_sort conditional relative survival in waldenström’s macroglobulinaemia: a population‐based study in the netherlands
topic Haematological malignancy–Clinical
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9297939/
https://www.ncbi.nlm.nih.gov/pubmed/34738239
http://dx.doi.org/10.1111/bjh.17926
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