Institute of Neuropathology, Charité - Universitätsmedizin Berlin, CVK, 13353 Berlin, Germany.
Biomaterials. 2009 Jan;30(1):52-7. doi: 10.1016/j.biomaterials.2008.09.044. Epub 2008 Oct 10.
Patients with glioblastoma multiforme (GBM), the most common primary brain tumor in adults, have still a poor prognosis though new strategies of radio- and chemotherapy have been developed. Recently, our group demonstrated the feasibility, tolerability and anti-tumoral effects of a newly developed therapeutic approach, termed thermotherapy using magnetic nanoparticles or magnetic fluid hyperthermia (MFH), in a murine model of malignant glioma. Currently, the efficacy of MFH is being evaluated in a phase II study. Here, we report on post-mortem neuropathological findings of patients with GBM receiving MFH. In brain autopsies the installed magnetic nanoparticles were dispersed or distributed as aggregates within geographic tumor necroses, restricted in distribution to the sites of instillation. Therefore, our results underscore the need for multiple trajectories of instillation. The typical GBM necrosis with pseudopalisading was free of particles. Dispersed particles and particle aggregates were phagocytosed mainly by macrophages whereas glioblastoma cells showed an uptake to a minor extent. MFH therapy further promotes uptake of nanoparticles in macrophages, likely as a consequence of tumor inherent and therapy induced formation of necrosis with subsequent infiltration and activation of phagocytes. We did not observe bystander effects of MFH such as sarcomatous tumour formation, formation of a sterile abscess or foreign body giant cell reaction. Furthermore, all patients did not present any clinical symptoms related to possible adverse effects of MFH.
尽管已经开发出新的放射和化学治疗策略,患有多形性胶质母细胞瘤(GBM)的患者,即成年人中最常见的原发性脑肿瘤,预后仍然较差。最近,我们的研究小组在恶性神经胶质瘤的小鼠模型中证明了一种新的治疗方法——使用磁性纳米粒子或磁流体热疗(MFH)的可行性、耐受性和抗肿瘤作用。目前,正在进行一项 II 期研究来评估 MFH 的疗效。在这里,我们报告了接受 MFH 的 GBM 患者的死后神经病理学发现。在脑尸检中,所安装的磁性纳米粒子在地理性肿瘤坏死区内呈分散或聚集分布,其分布仅限于注入部位。因此,我们的结果强调了需要进行多次注入轨迹。典型的 GBM 坏死伴假栅状排列无颗粒。分散的颗粒和颗粒聚集体主要被巨噬细胞吞噬,而胶质母细胞瘤细胞摄取程度较小。MFH 治疗进一步促进了巨噬细胞中纳米颗粒的摄取,可能是由于肿瘤固有和治疗诱导的坏死形成,随后浸润和激活吞噬细胞所致。我们没有观察到 MFH 的旁观者效应,例如肉瘤样肿瘤形成、无菌性脓肿形成或异物巨细胞反应。此外,所有患者均未出现任何与 MFH 可能的不良反应相关的临床症状。