Mayr Lisa, Guntner Armin S, Madlener Sibylle, Schmook Maria T, Peyrl Andreas, Azizi Amedeo A, Dieckmann Karin, Reisinger Dominik, Stepien Natalia M, Schramm Kathrin, Laemmerer Anna, Jones David T W, Ecker Jonas, Sahm Felix, Milde Till, Pajtler Kristian W, Blattner-Johnson Mirjam, Strbac Miroslav, Dorfer Christian, Czech Thomas, Kirchhofer Dominik, Gabler Lisa, Berger Walter, Haberler Christine, Müllauer Leonhard, Buchberger Wolfgang, Slavc Irene, Lötsch-Gojo Daniela, Gojo Johannes
Department of Pediatrics and Adolescent Medicine and Comprehensive Center for Pediatrics, Medical University of Vienna, 1090 Vienna, Austria.
Department of Medicine I, Institute of Cancer Research, Medical University of Vienna, 1090 Vienna, Austria.
J Pers Med. 2020 Dec 18;10(4):290. doi: 10.3390/jpm10040290.
Targeting oncogenic fusion-genes in pediatric high-grade gliomas (pHGG) with entrectinib has emerged as a highly promising therapeutic approach. Despite ongoing clinical studies, to date, no reports on the treatment of cerebrospinal fluid (CSF) disseminated fusion-positive pHGG exist. Moreover, clinically important information of combination with other treatment modalities such as intrathecal therapy, radiotherapy and other targeted agents is missing. We report on our clinical experience of entrectinib therapy in two CSF disseminated -fusion-positive pHGG cases. Combination of entrectinib with radiotherapy or intrathecal chemotherapy appears to be safe and has the potential to act synergistically with entrectinib treatment. In addition, we demonstrate CSF penetrance of entrectinib for the first time in patient samples suggesting target engagement even upon CSF dissemination. Moreover, in vitro analyses of two novel cell models derived from one case with -fusion revealed that combination therapy with either a MEK (trametinib) or a CDK4/6 (abemaciclib) inhibitor synergistically enhances entrectinib anticancer effects. In summary, our comprehensive study, including clinical experience, CSF penetrance and in vitro data on entrectinib therapy of -fusion-positive pHGG, provides essential clinical and preclinical insights into the multimodal treatment of these highly aggressive tumors. Our data suggest that combined inhibition of and other therapeutic vulnerabilities enhances the antitumor effect, which should be followed-up in further preclinical and clinical studies.
使用恩曲替尼靶向治疗儿童高级别胶质瘤(pHGG)中的致癌融合基因已成为一种极具前景的治疗方法。尽管临床研究仍在进行,但迄今为止,尚无关于脑脊液(CSF)播散性融合阳性pHGG治疗的报道。此外,与鞘内治疗、放疗和其他靶向药物等其他治疗方式联合使用的重要临床信息也缺失。我们报告了恩曲替尼治疗两例脑脊液播散性融合阳性pHGG病例的临床经验。恩曲替尼与放疗或鞘内化疗联合使用似乎是安全的,并且有可能与恩曲替尼治疗产生协同作用。此外,我们首次在患者样本中证明了恩曲替尼的脑脊液渗透性,表明即使在脑脊液播散时也能实现靶点结合。此外,对一例融合病例衍生的两种新型细胞模型进行的体外分析表明,与MEK(曲美替尼)或CDK4/6(阿贝西利)抑制剂联合治疗可协同增强恩曲替尼的抗癌效果。总之,我们的综合研究,包括临床经验、脑脊液渗透性以及融合阳性pHGG恩曲替尼治疗的体外数据,为这些高度侵袭性肿瘤的多模式治疗提供了重要的临床和临床前见解。我们的数据表明,联合抑制和其他治疗弱点可增强抗肿瘤作用,这应在进一步的临床前和临床研究中进行随访。