脑胶质瘤间质性激光照射的神经生物学背景、技术和典型结果

W. von Tempelhoff, F. Ulrich, H. Schwarzmaier
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引用次数: 2

摘要

背景:胶质瘤是最常见的原发性脑肿瘤类型。对于不适合开放显微手术的患者,已接受放化疗,激光照射已被证明是一种替代的姑息治疗选择。从1997年夏天到2006年冬天,我们进行了大约60次激光间质热疗法(LITT)治疗,从没有其他治疗选择的大型复发肿瘤患者开始。在本文中,我们报告神经生物学背景,技术和我们的经验,在脑胶质瘤的LITT。材料和方法:激光照射时,我们使用专门设计的光导(LITT标准涂敷器);Trumpf Medizintechnik, Umkirch,德国)。这种光导的尖端是一个特殊的光漫射器,其特征是均匀的球形或椭球发射轮廓。将光导引入适当的保护套(Somatex, Teltow,德国)。对于激光光源,我们采用连续波1064 nm Nd:YAG激光器(mediLas光纤4060 N;Dornier MedTech,德国魏陵)。全身麻醉下,在0.5 T开放构型磁共振(Signa SP;通用电气,密尔沃基,威斯康星州,美国)。通常,使用内置的定位系统(Flashpoint 3000;IGT, Boulder, CO, USA),在适当的情况下,与专门设计的导航系统(Localite™,Bonn, Germany)相结合。然后利用t1加权序列的多平面重建来控制光导的位置。为了实现近实时控制,使用基于MR信号的温度相关位移的实验软件包进行温度监测。当温度监测显示加热组织内的稳态温度分布时,停止激光照射。自2008年以来,我们使用传统的立体定向靶向和蛋氨酸正电子发射断层扫描/计算机断层扫描(MET-PET/CT)代替“开放式”MR系统来计划和随访脑肿瘤的LITT。结果:20世纪90年代初,我们开始了LITT治疗胶质瘤(良性胶质瘤在雄辩区/不适合手术)。1997年,我们开始治疗复发性胶质母细胞瘤/间变性胶质瘤。与恶性胶质瘤的自然病程相比,所有这些患者的生存率都有所提高。没有手术相关的死亡或永久性的神经功能缺损。对于LITT手术的整体成功来说,两个因素似乎很重要:1)在诊断出肿瘤复发后,尽早接受LITT治疗;2)在治疗开始时,相应的肿瘤肿块较小。结论:激光照射细胞减少术是治疗胶质瘤的一种很有前途的方法。
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Interstitial laser irradiation of cerebral gliomas – neurobiological background, technique and typical results
Abstract Background: The most common type of primary brain tumors are gliomas. For patients unsuitable for open microsurgery having been treated by radiochemotherapy, laser irradiation has proven to be an alternative palliative option. From summer 1997 until winter 2006 we performed about 60 laser-interstitial thermotherapy (LITT) treatments, starting with patients with large recurrent tumors who had no other therapeutic option. In the present article we report about the neurobiological background, the technique and our experience with LITT of cerebral gliomas. Materials and method: For laser irradiation we used a specially designed light guide (LITT standard applicator; Trumpf Medizintechnik, Umkirch, Germany). The tip of this light guide is a special optical diffuser which is characterized by a homogeneous spherical or ellipsoid emission profile. The light guide was introduced into an appropriate protective sheath (Somatex, Teltow, Germany). For the laser light source, we used a continuous wave 1064-nm Nd:YAG laser (mediLas fibertom 4060 N; Dornier MedTech, Weßling, Germany). Laser irradiation was performed under general anesthesia in a 0.5 T open configuration magnetic resonance (MR) system (Signa SP; General Electric, Milwaukee, WI, USA). Usually, the tip of the light guide was positioned in the center of the tumor using the built-in localization system (Flashpoint 3000; IGT, Boulder, CO, USA) in combination, where appropriate, with a specially designed navigation system (Localite™, Bonn, Germany). The position of the light guide was then controlled using multiplanar reconstructions of T1-weighted sequences. For near real-time control, temperature monitoring was performed using an experimental software package based on the temperature-dependent shift of the MR signal. Laser irradiation was ceased when the temperature monitoring revealed a steady state temperature profile within the heated tissue. Since 2008 we have used traditional stereotactic targeting and methionine positron emission tomography/computed tomography (MET-PET/CT) instead of the ‘open’ MR system for planning and follow-up in LITT of brain tumors. Results: We started the LITT treatment of gliomas in the early 1990s (benign gliomas in eloquent regions/not suitable for surgery). In 1997 we started to treat patients with recurrent gliobastomas/anaplastic gliomas. All of these patients had an increased survival in comparison to the natural course of recurrent glioblastomas. There were no procedure-related deaths or permanent neurological deficits. Two factors seem to be important for the overall success of the LITT procedure: 1) an early enrollment in the LITT therapy after diagnosis of a tumor recurrence, and 2) a corresponding smaller tumor mass at the beginning of the therapy. Conclusion: Cytoreduction by laser irradiation seems to be a promising option for patients suffering from gliomas.
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