Tejada Sonia, Díez-Valle Ricardo, Domínguez Pablo D, Patiño-García Ana, González-Huarriz Marisol, Fueyo Juan, Gomez-Manzano Cande, Idoate Miguel Angel, Peterkin Joanna, Alonso Marta M
Department of Neurosurgery, University Hospital of Navarra, Pamplona, Spain.
The Health Research Institute of Navarra (IDISNA), Pamplona, Spain.
Front Oncol. 2018 Mar 12;8:61. doi: 10.3389/fonc.2018.00061. eCollection 2018.
Diffuse intrinsic pontine gliomas (DIPGs) are aggressive glial brain tumors that primarily affect children, for which there is no curative treatment. Median overall survival is only one year. Currently, the scientific focus is on expanding the knowledge base of the molecular biology of DIPG, and identifying effective therapies. Oncolytic adenovirus DNX-2401 is a replication-competent, genetically modified virus capable of infecting and killing glioma cells, and stimulating an anti-tumor immune response. Clinical trials evaluating intratumoral DNX-2401 in adults with recurrent glioblastoma have demonstrated that the virus has a favorable safety profile and can prolong survival. Subsequently, these results have encouraged the transition of this biologically active therapy from adults into the pediatric population. To this aim, we have designed a clinical Phase I trial for newly diagnosed pediatric DIPG to investigate the feasibility, safety, and preliminary efficacy of delivering DNX-2401 into tumors within the pons following biopsy. This case report presents a pediatric patient enrolled in this ongoing Phase I trial for children and adolescents with newly diagnosed DIPG. The case involves an 8-year-old female patient with radiologically diagnosed DIPG who underwent stereotactic tumor biopsy immediately followed by intratumoral DNX-2401 in the same biopsy track. Because there were no safety concerns or new neurological deficits, the patient was discharged 3 days after the procedures. To our knowledge, this is the first report of intratumoral DNX-2401 for a patient with DIPG in a clinical trial. We plan to demonstrate that intratumoral delivery of an oncolytic virus following tumor biopsy for pediatric patients with DIPG is a novel and feasible approach and that DNX-2401 represents an innovative treatment for the disease.
弥漫性脑桥内在型胶质瘤(DIPG)是一种侵袭性胶质脑瘤,主要影响儿童,目前尚无治愈性治疗方法。中位总生存期仅为一年。目前,科学研究的重点是扩大对DIPG分子生物学的认识,并确定有效的治疗方法。溶瘤腺病毒DNX-2401是一种具有复制能力的基因改造病毒,能够感染并杀死胶质瘤细胞,并刺激抗肿瘤免疫反应。评估瘤内注射DNX-2401治疗复发性胶质母细胞瘤成年患者的临床试验表明,该病毒具有良好的安全性,并且可以延长生存期。随后,这些结果促使这种生物活性疗法从成人转向儿科患者群体。为此,我们设计了一项针对新诊断的儿科DIPG的临床I期试验,以研究在活检后将DNX-2401注入脑桥肿瘤内的可行性、安全性和初步疗效。本病例报告介绍了一名参与这项正在进行的针对新诊断DIPG的儿童和青少年I期试验的儿科患者。该病例涉及一名8岁女性患者,经放射学诊断为DIPG,她接受了立体定向肿瘤活检,随后在同一活检通道内进行了瘤内DNX-2401注射。由于没有安全问题或新的神经功能缺损,患者在手术后3天出院。据我们所知,这是在临床试验中首例将DNX-2401瘤内注射用于DIPG患者的报告。我们计划证明,对于儿科DIPG患者,在肿瘤活检后进行瘤内溶瘤病毒注射是一种新颖且可行的方法,并且DNX-2401代表了针对该疾病的一种创新治疗方法。