Literature DB >> 29349612

Dexamethasone-induced leukocytosis is associated with poor survival in newly diagnosed glioblastoma.

Daniel Dubinski1,2, Sae-Yeon Won3, Florian Gessler3, Johanna Quick-Weller3, Bedjan Behmanesh3, Simon Bernatz4, Marie-Therese Forster3, Kea Franz3, Karl-Heinz Plate4,5, Volker Seifert3, Patrick N Harter4,5, Christian Senft3.   

Abstract

Despite its well-characterized side effects, dexamethasone is widely used in the pre-, peri- and postoperative neurosurgical setting due to its effective relief of tumor-induced symptoms through the reduction of tumor-associated edema. However, some patients show laboratory-defined dexamethasone induced elevation of white blood cell count, and its impact on glioblastoma progression is unknown. We retrospectively analyzed 113 patients with newly diagnosed glioblastoma to describe the incidence, risk factors and clinical features of dexamethasone-induced leukocytosis in primary glioblastoma patients. We further conducted an immunohistochemical analysis of the granulocyte and lymphocyte tumor-infiltration in the available corresponding histological sections. Patient age was identified to be a risk factor for the development of dexamethasone-induced leukocytosis (p < 0.05). The presence of dexamethasone-induced leukocytosis decreased overall survival (HR 2.25 95% CI [1.15-4.38]; p < 0.001) and progression-free survival (HR 2.23 95% CI [1.09-4.59]; p < 0.01). Furthermore, patients with dexamethasone-induced leukocytosis had significantly reduced CD15 + granulocytic- (p < 0.05) and CD3 + lymphocytic tumour infiltration (p < 0.05). We identified a subgroup of glioblastoma patients that are at particularly high risk for poor outcome upon dexamethasone treatment. Therefore, restrictive dosage or other edema reducing substances should be considered in patients with dexamethasone-induced leukocytosis.

Entities:  

Keywords:  Cerebral edema; Glioblastoma; Leukocytosis; Survival; Tumor-infiltration

Mesh:

Substances:

Year:  2018        PMID: 29349612     DOI: 10.1007/s11060-018-2761-4

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  25 in total

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