Department of Radiation Oncology, University Medical Center Leipzig, Stephan-Str. 9a, 04103, Leipzig, Germany.
Strahlenther Onkol. 2013 Aug;189(8):693-6. doi: 10.1007/s00066-013-0370-x. Epub 2013 Jun 12.
Primary metastatic diffuse intrinsic pontine glioma (DIPG) is relatively rare and associated with a dismal prognosis. Combining craniospinal irradiation (CSI) with concurrent temozolomide and nimotuzumab therapy may slightly improve tumor control and overall survival. However, little is known about the feasibility and toxicity of this treatment approach. Here, we describe the case of an 8-year-old girl with primary metastatic DIPG who received craniospinal radiotherapy, a local boost, and concurrent temozolomide and nimotuzumab treatment based on an individual therapy recommendation. Radiotherapy could be completed without any interruption. However, concurrent temozolomide had to be disrupted several times due to considerable acute myelotoxicity (grade III-IV).Maintenance immunochemotherapy could be started with a delay of 5 days and was performed according to treatment schedule. The disease could be stabilized for a few months. A routine MRI scan finally depicted disease progression 5.7 months after the start of irradiation. The patient died 1.9 months later.
原发性弥散性桥脑内胶质瘤(DIPG)的原发性转移较为罕见,预后较差。颅脊髓放疗(CSI)联合替莫唑胺和顺铂治疗可能会稍微提高肿瘤控制率和总生存率。然而,目前对于这种治疗方法的可行性和毒性还知之甚少。在这里,我们描述了一例 8 岁女孩的病例,她患有原发性转移性 DIPG,根据个体化治疗建议,接受了颅脊髓放疗、局部加量放疗以及替莫唑胺和顺铂的同步治疗。放疗可以顺利完成,没有任何中断。然而,由于严重的骨髓抑制毒性(III-IV 级),替莫唑胺的同步治疗不得不中断数次。免疫化疗的维持治疗可以延迟 5 天开始,并按照治疗方案进行。疾病在几个月内得到了稳定。常规 MRI 扫描最终显示,在放疗开始后 5.7 个月出现疾病进展。患者在 1.9 个月后死亡。