Selvik Henriette Aurora, Thomassen Lars, Bjerkreim Anna Therese, Næss Halvor
Department of Clinical Medicine, University of Bergen, Bergen, Norway ; Department of Neurology, Haukeland University Hospital, Bergen, Norway.
Department of Clinical Medicine, University of Bergen, Bergen, Norway ; Department of Neurology, Haukeland University Hospital, Bergen, Norway ; Centre for Age-Related Medicine, Stavanger University Hospital, Stavanger, Norway.
Cerebrovasc Dis Extra. 2015 Oct 13;5(3):107-13. doi: 10.1159/000440730. eCollection 2015 Sep-Dec.
Underlying malignancy can cause ischemic stroke in some patients. Mechanisms include the affection of the coagulation cascade, tumor mucin secretion, infections and nonbacterial endocarditis. The release of necrotizing factor and interleukins may cause inflammation of the endothelial lining, creating a prothrombotic surface that triggers thromboembolic events, including stroke. The aims of this study were to assess the occurrence of cancer in patients who had recently suffered an ischemic stroke and to detect possible associations between stroke and cancer subtypes.
All ischemic stroke patients registered in the Norwegian Stroke Research Registry (NORSTROKE) as part of the ongoing Bergen NORSTROKE study were included. Blood samples were obtained on admission. Stroke etiology was determined by the Trial of Org 10172 in Acute Stroke Treatment (TOAST) criteria, and the severity of stroke was defined according to the National Institute of Health Stroke Scale score. Information about cancer disease after stroke was obtained from patient medical records and The Cancer Registry of Norway.
From a total of 1,282 ischemic stroke patients with no history of cancer, 55 (4.3%) patients were diagnosed with cancer after stroke. The median time from stroke onset to cancer diagnosis was 14.0 months (interquartile range 6.2-24.5). Twenty-three (41.8%) patients were diagnosed with cancer within 1 year and 13 (23.6%) within 6 months. The most common cancer type was lung cancer (19.0%). By Cox regression analysis, cancer after stroke was associated with elevated D-dimer levels on admittance (p < 0.001), age (p = 0.01) and smoking (p = 0.04).
Cancer-associated stroke is rare, and routine investigation for cancer seems unwarranted in acute ischemic stroke. However, in stroke patients with elevated levels of blood coagulation factors, C-reactive protein, higher age and a history of smoking, underlying malignancy should be considered. Our study suggests that an unknown stroke etiology does not predict malignancy.
潜在恶性肿瘤可导致部分患者发生缺血性卒中。其机制包括凝血级联反应受影响、肿瘤黏液分泌、感染及非细菌性心内膜炎。坏死因子和白细胞介素的释放可能导致血管内皮炎症,形成促血栓表面,引发包括卒中在内的血栓栓塞事件。本研究的目的是评估近期发生缺血性卒中患者的癌症发生率,并检测卒中与癌症亚型之间可能存在的关联。
纳入挪威卒中研究登记处(NORSTROKE)登记的所有缺血性卒中患者,这些患者是正在进行的卑尔根NORSTROKE研究的一部分。入院时采集血样。根据急性卒中治疗中组织纤溶酶原激活剂10172试验(TOAST)标准确定卒中病因,根据美国国立卫生研究院卒中量表评分定义卒中严重程度。卒中后癌症疾病信息来自患者病历和挪威癌症登记处。
在1282例无癌症病史的缺血性卒中患者中,55例(4.3%)患者在卒中后被诊断为癌症。从卒中发作到癌症诊断的中位时间为14.0个月(四分位间距6.2 - 24.5)。23例(41.8%)患者在1年内被诊断为癌症,13例(23.6%)在6个月内被诊断为癌症。最常见的癌症类型是肺癌(19.0%)。通过Cox回归分析,卒中后癌症与入院时D - 二聚体水平升高(p < 0.001)、年龄(p = 0.01)和吸烟(p = 0.04)相关。
癌症相关性卒中罕见,急性缺血性卒中患者常规进行癌症检查似乎没有必要。然而,对于凝血因子水平升高、C反应蛋白升高、年龄较大且有吸烟史的卒中患者,应考虑潜在恶性肿瘤。我们的研究表明,不明原因的卒中病因不能预测恶性肿瘤。