胶质母细胞瘤患者的循环肿瘤细胞与血栓栓塞事件

Christina C. Rolling, Malte Mohme, Carsten Bokemeyer, Manfred Westphal, Sabine Riethdorf, Katrin Lamszus, Klaus Pantel, Felix Klingler, Florian Langer
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摘要

胶质母细胞瘤(GBM)患者发生动脉和静脉血栓栓塞症(TE)的风险增加。风险因素包括手术、使用皮质类固醇、放疗和化疗,以及肿瘤本身的促血栓形成特征,如组织因子、血管内皮生长因子或 podoplanin 的表达。虽然在这种肿瘤实体中远处转移极为罕见,但在相当一部分 GBM 患者中检测到了循环肿瘤细胞(CTC),这可能将局部肿瘤生长特征与全身高凝状态联系起来。我们对一项研究进行了事后分析,该研究对 GBM 患者进行了 CTCs 调查。我们从电子病历中检索了有关 TE 的信息。共分析了 133 名患者(中位年龄 63 岁;四分位数区间 53-70 岁)。在随访期间,有 14 名患者(11%)记录到 TE,其中包括 8 例静脉事件和 6 例动脉事件。26名患者(20%)检测到了四氯化碳。与 10 例(9%)无 CTC 的患者相比,4 例(15%)有 CTC 的患者发生了 TE。检测到和未检测到 CTCs 的患者发生 TE 事件的频率没有差异(p = 0.58)。总之,尽管我们的研究证实了 GBM 患者发生 TE 的风险很高,但并没有指出 CTC 与血管血栓之间存在明显的关联。
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Circulating Tumor Cells and Thromboembolic Events in Patients with Glioblastoma

Patients with glioblastoma (GBM) are at increased risk for arterial and venous thromboembolism (TE). Risk factors include surgery, the use of corticosteroids, radiation, and chemotherapy, but also prothrombotic characteristics of the tumor itself such as expression of tissue factor, vascular endothelial growth factor, or podoplanin. Although distant metastases are extremely rare in this tumor entity, circulating tumor cells (CTCs) have been detected in a significant proportion of GBM patients, potentially linking local tumor growth characteristics to systemic hypercoagulability. We performed post hoc analysis of a study, in which GBM patients had been investigated for CTCs. Information on TE was retrieved from electronic patient charts. In total, 133 patients (median age, 63 years; interquartile range, 53–70 years) were analyzed. During follow-up, TE was documented in 14 patients (11%), including 8 venous and 6 arterial events. CTCs were detected in 26 patients (20%). Four (15%) patients with CTCs had a TE compared with 10 (9%) patients without CTCs. There was no difference in the frequency of TE events between patients with and those without detectable CTCs (p = 0.58). In summary, although our study confirms a high risk of TE in GBM patients, it does not point to an obvious association between CTCs and vascular thrombosis.

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