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Diffuse, non-traumatic, non-aneurysmal subarachnoid haemorrhage during bevacizumab treatment of high grade glioma: case report and review of the literature

机译:贝伐单抗治疗高级神经胶质瘤期间弥漫性,非创伤性,非动脉瘤性蛛网膜下腔出血:病例报告及文献复习

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Background: Bevacizumab is a monoclonal antibody against vascular endothelial growth factor approved by the United States Food and Drug Administration for the treatment of various cancers including refractory high grade glioma. There are case reports of subarachnoid haemorrhage (SAH) during bevacizumab treatment though the causative role of the drug in these cases has been obscured by the presence of alternative aetiologies or incomplete investigation. Furthermore, there is no consensus regarding the risk of Central Nervous System (CNS) haemorrhage during bevacizumab treatment due to limited available study data. Case Description: A 53year old female with recurrent gliosarcoma refractory to standard, temozolamide based chemo-radiotherapy presented to our facility in a post-ictal state 16days after her second dose of intravenous bevacizumab. A Fisher grade III SAH was found on computerised tomography scanning with no causative vascular lesion found on two subsequent digital subtraction angiograms separated by a 10day period and a Magnetic Resonance Imaging (MRI) scan 20days post-bleed. Given the resolution of symptoms over an uncomplicated 13day admission, she was discharged home with bevacizumab ceased prior to her scheduled third dose. Conclusion: We discuss here a case of diffuse, non-traumatic SAH during bevacizumab treatment of recurrent gliosarcoma in which alternative aetiologies of haemorrhage were excluded, to our knowledge the first such case in the English language literature. This adverse event is compatible with the known molecular mechanisms of bevacizumab and clinicians should be cognisant of the potential risk of CNS haemorrhage until larger studies are available to quantify this risk. Highlights ? First report of diffuse subarachnoid haemorrhage of no other cause during bevacizumab therapy. ? No current consensus on the risk of Central Nervous System haemorrhage during bevacizumab therapy. ? Promotion of vessel defects, vasoconstriction and hypertension are likely causative mechanisms. ? Clinicians should be cognisant of this potential adverse effect while further studies are awaited.
机译:背景:贝伐单抗是一种抗血管内皮生长因子的单克隆抗体,已获得美国食品和药物管理局的批准,可用于治疗各种癌症,包括难治性高级别神经胶质瘤。贝伐单抗治疗期间有蛛网膜下腔出血(SAH)的病例报告,尽管在这些病例中药物的致病作用已被其他病因或调查不彻底所掩盖。此外,由于有限的可用研究数据,在贝伐单抗治疗期间中枢神经系统(CNS)出血的风险尚无共识。病例描述:一名53岁女性,复发性青光眼肉眼难治,其标准剂量是基于替莫唑胺的化学放射疗法,第二次静脉注射贝伐单抗治疗后16天,在发作后就诊。在计算机断层扫描中发现了Fisher III级SAH,在出血后20天连续两次相隔10天的数字减影血管造影和磁共振成像(MRI)扫描中未发现致病性血管病变。鉴于经过13天的简单入院即可缓解症状,因此她在出院第三次服药前停止了贝伐单抗的出院。结论:我们在此讨论贝伐单抗治疗复发性眼胶质瘤期间发生弥漫性,非创伤性SAH的情况,其中排除了出血的其他病因,据我们所知,这是英语文献中的首例此类情况。该不良事件与贝伐单抗的已知分子机制相符,并且临床医生应意识到中枢神经系统出血的潜在风险,直到有更大的研究来量化这种风险为止。强调 ?贝伐单抗治疗期间无其他原因的弥漫性蛛网膜下腔出血的首次报道。 ?贝伐单抗治疗期间中枢神经系统出血的风险目前尚无共识。 ?促进血管缺损,血管收缩和高血压可能是其致病机制。 ?在等待进一步研究的同时,临床医生应意识到这种潜在的不良反应。

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