Department of Neurosurgery, University Hospital, Goethe University, Schleusenweg 2-16, 60528, Frankfurt am Main, Germany.
Institute of Neurology (Edinger Institute), Goethe University, Frankfurt am Main, Germany.
J Neurooncol. 2018 May;137(3):503-510. doi: 10.1007/s11060-018-2761-4. Epub 2018 Jan 18.
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.
尽管地塞米松具有明确的副作用,但由于其通过减少肿瘤相关水肿有效缓解肿瘤引起的症状,因此在神经外科围手术期被广泛用于治疗。然而,一些患者表现出实验室定义的地塞米松诱导的白细胞计数升高,但其对胶质母细胞瘤进展的影响尚不清楚。我们回顾性分析了 113 例新诊断的胶质母细胞瘤患者,以描述原发性胶质母细胞瘤患者中地塞米松诱导性白细胞增多的发生率、危险因素和临床特征。我们进一步对可用的相应组织学切片进行了粒细胞和淋巴细胞肿瘤浸润的免疫组织化学分析。患者年龄被确定为地塞米松诱导性白细胞增多发生的危险因素(p<0.05)。地塞米松诱导性白细胞增多的存在降低了总生存期(HR 2.25,95%CI [1.15-4.38];p<0.001)和无进展生存期(HR 2.23,95%CI [1.09-4.59];p<0.01)。此外,地塞米松诱导性白细胞增多的患者 CD15+粒细胞肿瘤浸润(p<0.05)和 CD3+淋巴细胞肿瘤浸润(p<0.05)显著减少。我们确定了一组胶质母细胞瘤患者,他们在地塞米松治疗后出现不良预后的风险特别高。因此,对于地塞米松诱导性白细胞增多的患者,应考虑限制剂量或使用其他减轻水肿的物质。