| Literature DB >> 33353026 |
Lisa Mayr1,2,3, Armin S Guntner4, Sibylle Madlener1,3, Maria T Schmook5, Andreas Peyrl1, Amedeo A Azizi1, Karin Dieckmann6, Dominik Reisinger1, Natalia M Stepien1, Kathrin Schramm7,8, Anna Laemmerer1,2,3, David T W Jones7,8, Jonas Ecker9, Felix Sahm10,11, Till Milde7,9, Kristian W Pajtler7,12,13, Mirjam Blattner-Johnson7,8, Miroslav Strbac14, Christian Dorfer15, Thomas Czech15, Dominik Kirchhofer1,2,3, Lisa Gabler2,3, Walter Berger2,3, Christine Haberler16, Leonhard Müllauer17, Wolfgang Buchberger4, Irene Slavc1, Daniela Lötsch-Gojo2,3,15, Johannes Gojo1,3,7,12.
Abstract
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 ROS1/NTRK-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 NTRK-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 NTRK/ROS1-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 NTRK/ROS1 and other therapeutic vulnerabilities enhances the antitumor effect, which should be followed-up in further preclinical and clinical studies.Entities:
Keywords: CSF penetrance; NTRK fusion; ROS1 fusion; abemaciclib; entrectinib; radiotherapy; targeted therapies; trametinib
Year: 2020 PMID: 33353026 PMCID: PMC7766483 DOI: 10.3390/jpm10040290
Source DB: PubMed Journal: J Pers Med ISSN: 2075-4426