Ening Genevieve, Osterheld Fransiska, Capper David, Schmieder Kirsten, Brenke Christopher
Department of Neurosurgery, Knappschafts-Krankenhaus Bochum-Langendreer, Ruhr-University of Bochum, In der Schornau 23-25, 44892 Bochum, Germany; Department of Neurosurgery, University Medical Center Mannheim, University of Heidelberg, Theodor-Kutzer-Ufer 1, 68167 Mannheim, Germany.
Department of Neurosurgery, University Medical Center Mannheim, University of Heidelberg, Theodor-Kutzer-Ufer 1, 68167 Mannheim, Germany.
Clin Neurol Neurosurg. 2015 Jul;134:55-9. doi: 10.1016/j.clineuro.2015.01.006. Epub 2015 Jan 9.
Thromboembolic events, seizures, neurologic symptoms and adverse effects from corticosteroids and chemotherapies are frequent clinical complications seen in Glioblastoma (GB) patients. The exact impact these have on dismal patient outcome has not been fully elucidated. We aimed at assessing treatment associated complications, evaluating the impact on survival and defining risk factors.
Two hundred and thirty three consecutive adult patients operated on for newly diagnosed GB at a single tertiary institution over a 5-year-period (2006-2011) were assessed. Demographic parameters (age, gender, comorbidity status quantified by the Charlson-comorbidity-index (CCI), functional status computed by the Karnofsky Performance Scale (KPS), tumor characteristics (size, location, IDH-1 mutation and MGMT-Promotor-methylation-status) and treatment parameters (volumetrically quantified extent of resection and adjuvant therapy) were retrospectively reviewed. Complications assessed were recorded as neurological (N), surgical (S) and medical (M). Independent risk factor analysis was performed by the univariate and multivariate logistic regression method. Survival analysis was plotted by the Kaplan-Meier-method, influence of complication occurrence was evaluated by the log-rank test.
One hundred and fifty nine (68.2%) patients had a total of 281 complications (90 N, 174 M and 17 S). Univariate analysis identified age (P=0.003), KPS<70 (P=0.002), CCI>3 (P=0.03), eloquent tumor location (P=0.001) and therapy other than the standard radio-chemotherapy with temozolomide therapy (P=0.034) as risk factors for complications. Multivariate analysis extracted the eloquent tumor location (P=0.007, odds ratio 1.94) as a significant predictor for complications. Having a complication significantly decreased patient survival (P=0.015).
Complications significantly decrease GB patient survival. Age, poor functional status, other than standard adjuvant therapy and eloquent tumor location proved as significant risk factors for encountering a therapy associated complication. Not extensive surgery or tumor size but surgery at eloquent locations impacts complication occurrence the strongest with a 2 fold increased complication occurrence risk.
血栓栓塞事件、癫痫发作、神经系统症状以及皮质类固醇和化疗的不良反应是胶质母细胞瘤(GB)患者常见的临床并发症。这些并发症对患者预后不良的确切影响尚未完全阐明。我们旨在评估与治疗相关的并发症,评估其对生存的影响并确定危险因素。
对一家三级医疗机构在5年期间(2006 - 2011年)连续接受手术治疗的233例新诊断为GB的成年患者进行评估。回顾性分析人口统计学参数(年龄、性别、由查尔森合并症指数(CCI)量化的合并症状态、由卡诺夫斯基表现量表(KPS)计算的功能状态)、肿瘤特征(大小、位置、异柠檬酸脱氢酶-1(IDH-1)突变和O6-甲基鸟嘌呤-DNA甲基转移酶(MGMT)启动子甲基化状态)以及治疗参数(体积量化的切除范围和辅助治疗)。评估的并发症记录为神经学并发症(N)、手术并发症(S)和医疗并发症(M)。通过单因素和多因素逻辑回归方法进行独立危险因素分析。采用Kaplan-Meier方法绘制生存分析图,通过对数秩检验评估并发症发生的影响。
159例(68.2%)患者共有281种并发症(90种神经学并发症、174种医疗并发症和17种手术并发症)。单因素分析确定年龄(P = 0.003)、KPS<70(P = 0.002)、CCI>3(P = 0.03)、明确的肿瘤位置(P = 0.001)以及除替莫唑胺标准放化疗之外的其他治疗(P = 0.034)为并发症的危险因素。多因素分析得出明确的肿瘤位置(P = 0.007,比值比1.94)是并发症的显著预测因素。发生并发症会显著降低患者生存率(P = 0.015)。
并发症显著降低GB患者的生存率。年龄、功能状态差、非标准辅助治疗以及明确的肿瘤位置被证明是发生与治疗相关并发症的显著危险因素。不是广泛的手术或肿瘤大小,而是明确位置的手术对并发症发生的影响最强,并发症发生风险增加2倍。