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Published in: Journal of Neuro-Oncology 1/2016

01-10-2016 | Clinical Study

White matter lesions reduce number of brain metastases in different cancers: a high-resolution MRI study

Authors: Benjamin-Andreas Berk, Sandra Nagel, K. Hering, S. Paschke, Karl-Titus Hoffmann, Rolf-Dieter Kortmann, Chiara Gaudino, Clemens Seidel

Published in: Journal of Neuro-Oncology | Issue 1/2016

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Abstract

Brain metastases are major complications of common cancers. Tumor type and proneness to the CNS are thought to define the number and size of brain metastases. It is not known if intrinsic vascular factors can also have an effect. Restricted perfusion due to cerebral small vessel disease is frequent in elderly patients and causes white matter lesions (WML). The aim of this analysis was to evaluate a possible negative effect of WML and patient age on the number and size of brain metastases (BM) of different tumor entities. Pre-therapeutic 3 T brain magnetic resonance imaging (MRI) of 200 patients with BM were analyzed. Location, size and number of BM (NoM) were determined. T2 hyperintensive WML were scored according to Fazekas-Score (grade I–III). Patients with WML grade 1 (NoM: 5.59; p = 0.009) and grade 2 (NoM: 3.68; p = 0.002) had significantly less BM than patients without WML (NoM: 6.99). This effect was present in subgroups of different tumors: NSCLC (p = 0.05), other tumors than NSCLC (p = 0.048). Age (≤65 or >65 years) was positively correlated with the degree of WML but not with number (pNoM = 0.832) or mean diameter (pmDM = 0.662) of brain metastases. While patient age did not appear to be relevant, increasing WML were associated with lower number of brain metastases in different tumor types.
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Metadata
Title
White matter lesions reduce number of brain metastases in different cancers: a high-resolution MRI study
Authors
Benjamin-Andreas Berk
Sandra Nagel
K. Hering
S. Paschke
Karl-Titus Hoffmann
Rolf-Dieter Kortmann
Chiara Gaudino
Clemens Seidel
Publication date
01-10-2016
Publisher
Springer US
Published in
Journal of Neuro-Oncology / Issue 1/2016
Print ISSN: 0167-594X
Electronic ISSN: 1573-7373
DOI
https://doi.org/10.1007/s11060-016-2235-5

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