Cargando…

An increased bone mineral density is an adverse prognostic factor in patients with systemic mastocytosis

PURPOSE: Systemic mastocytosis (SM) is characterized by the expansion of clonal mast cells that infiltrate various organ systems. The extent of organ infiltration and subsequent organ damage distinguishes between indolent SM (ISM) defined by a nearly normal life expectancy and advanced SM (AdvSM) de...

Descripción completa

Detalles Bibliográficos
Autores principales: Riffel, Philipp, Schwaab, Juliana, Lutz, Christopher, Naumann, Nicole, Metzgeroth, Georgia, Fabarius, Alice, Schoenberg, Stefan O., Hofmann, Wolf-Karsten, Valent, Peter, Reiter, Andreas, Jawhar, Mohamad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7085471/
https://www.ncbi.nlm.nih.gov/pubmed/31980928
http://dx.doi.org/10.1007/s00432-019-03119-3
_version_ 1783508941325467648
author Riffel, Philipp
Schwaab, Juliana
Lutz, Christopher
Naumann, Nicole
Metzgeroth, Georgia
Fabarius, Alice
Schoenberg, Stefan O.
Hofmann, Wolf-Karsten
Valent, Peter
Reiter, Andreas
Jawhar, Mohamad
author_facet Riffel, Philipp
Schwaab, Juliana
Lutz, Christopher
Naumann, Nicole
Metzgeroth, Georgia
Fabarius, Alice
Schoenberg, Stefan O.
Hofmann, Wolf-Karsten
Valent, Peter
Reiter, Andreas
Jawhar, Mohamad
author_sort Riffel, Philipp
collection PubMed
description PURPOSE: Systemic mastocytosis (SM) is characterized by the expansion of clonal mast cells that infiltrate various organ systems. The extent of organ infiltration and subsequent organ damage distinguishes between indolent SM (ISM) defined by a nearly normal life expectancy and advanced SM (AdvSM) defined by poor prognosis. In ISM, measurement of the bone mineral density (BMD) frequently reveals osteoporosis. In contrast, the clinical implication of an increased BMD and osteosclerosis remains unclear. METHODS: BMD was evaluated in 61 patients with mastocytosis (ISM, n = 29, 48%; AdvSM, n = 32, 52%). We correlated the prevalence of osteoporosis, increased BMD and osteosclerosis with clinical parameters, disease variant and prognosis. RESULTS: Osteoporosis was detected in 11/29 (38%) patients with ISM but only in 2/32 (6%) patients with AdvSM (p = 0.004). An increased BMD was detected in 1/29 (3%) patients with ISM and 24/32 (75%) patients with AdvSM (p < 0.001) while osteosclerosis was only detected in AdvSM patients (16/32, 50%). AdvSM patients with increased BMD had higher levels of bone marrow mast cell infiltration, higher serum tryptase and alkaline phosphatase levels compared to ISM as well as higher number of high-molecular risk mutations (p < 0.05). In addition, we found that the prognosis of AdvSM patients with increased BMD is inferior compared to those without increased BMD (median overall survival 3.6 years versus not reached, p = 0.031). CONCLUSIONS: Osteoporosis is a common feature in ISM but not in AdvSM. An increased BMD is frequently present in AdvSM but not in ISM and is associated with more advanced disease and inferior outcome.
format Online
Article
Text
id pubmed-7085471
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-70854712020-03-23 An increased bone mineral density is an adverse prognostic factor in patients with systemic mastocytosis Riffel, Philipp Schwaab, Juliana Lutz, Christopher Naumann, Nicole Metzgeroth, Georgia Fabarius, Alice Schoenberg, Stefan O. Hofmann, Wolf-Karsten Valent, Peter Reiter, Andreas Jawhar, Mohamad J Cancer Res Clin Oncol Original Article – Clinical Oncology PURPOSE: Systemic mastocytosis (SM) is characterized by the expansion of clonal mast cells that infiltrate various organ systems. The extent of organ infiltration and subsequent organ damage distinguishes between indolent SM (ISM) defined by a nearly normal life expectancy and advanced SM (AdvSM) defined by poor prognosis. In ISM, measurement of the bone mineral density (BMD) frequently reveals osteoporosis. In contrast, the clinical implication of an increased BMD and osteosclerosis remains unclear. METHODS: BMD was evaluated in 61 patients with mastocytosis (ISM, n = 29, 48%; AdvSM, n = 32, 52%). We correlated the prevalence of osteoporosis, increased BMD and osteosclerosis with clinical parameters, disease variant and prognosis. RESULTS: Osteoporosis was detected in 11/29 (38%) patients with ISM but only in 2/32 (6%) patients with AdvSM (p = 0.004). An increased BMD was detected in 1/29 (3%) patients with ISM and 24/32 (75%) patients with AdvSM (p < 0.001) while osteosclerosis was only detected in AdvSM patients (16/32, 50%). AdvSM patients with increased BMD had higher levels of bone marrow mast cell infiltration, higher serum tryptase and alkaline phosphatase levels compared to ISM as well as higher number of high-molecular risk mutations (p < 0.05). In addition, we found that the prognosis of AdvSM patients with increased BMD is inferior compared to those without increased BMD (median overall survival 3.6 years versus not reached, p = 0.031). CONCLUSIONS: Osteoporosis is a common feature in ISM but not in AdvSM. An increased BMD is frequently present in AdvSM but not in ISM and is associated with more advanced disease and inferior outcome. Springer Berlin Heidelberg 2020-01-24 2020 /pmc/articles/PMC7085471/ /pubmed/31980928 http://dx.doi.org/10.1007/s00432-019-03119-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article – Clinical Oncology
Riffel, Philipp
Schwaab, Juliana
Lutz, Christopher
Naumann, Nicole
Metzgeroth, Georgia
Fabarius, Alice
Schoenberg, Stefan O.
Hofmann, Wolf-Karsten
Valent, Peter
Reiter, Andreas
Jawhar, Mohamad
An increased bone mineral density is an adverse prognostic factor in patients with systemic mastocytosis
title An increased bone mineral density is an adverse prognostic factor in patients with systemic mastocytosis
title_full An increased bone mineral density is an adverse prognostic factor in patients with systemic mastocytosis
title_fullStr An increased bone mineral density is an adverse prognostic factor in patients with systemic mastocytosis
title_full_unstemmed An increased bone mineral density is an adverse prognostic factor in patients with systemic mastocytosis
title_short An increased bone mineral density is an adverse prognostic factor in patients with systemic mastocytosis
title_sort increased bone mineral density is an adverse prognostic factor in patients with systemic mastocytosis
topic Original Article – Clinical Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7085471/
https://www.ncbi.nlm.nih.gov/pubmed/31980928
http://dx.doi.org/10.1007/s00432-019-03119-3
work_keys_str_mv AT riffelphilipp anincreasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT schwaabjuliana anincreasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT lutzchristopher anincreasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT naumannnicole anincreasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT metzgerothgeorgia anincreasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT fabariusalice anincreasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT schoenbergstefano anincreasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT hofmannwolfkarsten anincreasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT valentpeter anincreasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT reiterandreas anincreasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT jawharmohamad anincreasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT riffelphilipp increasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT schwaabjuliana increasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT lutzchristopher increasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT naumannnicole increasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT metzgerothgeorgia increasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT fabariusalice increasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT schoenbergstefano increasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT hofmannwolfkarsten increasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT valentpeter increasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT reiterandreas increasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis
AT jawharmohamad increasedbonemineraldensityisanadverseprognosticfactorinpatientswithsystemicmastocytosis