Literature DB >> 33353026

Cerebrospinal Fluid Penetration and Combination Therapy of Entrectinib for Disseminated ROS1/NTRK-Fusion Positive Pediatric High-Grade Glioma.

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


  2 in total

1.  Novel Insights into Diagnosis, Biology and Treatment of Primary Diffuse Leptomeningeal Melanomatosis.

Authors:  Alicia Baumgartner; Natalia Stepien; Lisa Mayr; Sibylle Madlener; Christian Dorfer; Maria T Schmook; Tatjana Traub-Weidinger; Daniela Lötsch-Gojo; Dominik Kirchhofer; Dominik Reisinger; Cora Hedrich; Saleha Arshad; Stefan Irschik; Heidrun Boztug; Gernot Engstler; Marie Bernkopf; Fikret Rifatbegovic; Christoph Höller; Irene Slavc; Walter Berger; Leonhard Müllauer; Christine Haberler; Amedeo A Azizi; Andreas Peyrl; Johannes Gojo
Journal:  J Pers Med       Date:  2021-04-12

2.  Targeting fibroblast growth factor receptors to combat aggressive ependymoma.

Authors:  Walter Berger; Johannes Gojo; Daniela Lötsch; Dominik Kirchhofer; Bernhard Englinger; Li Jiang; Konstantin Okonechnikov; Daniel Senfter; Anna Laemmerer; Lisa Gabler; Christine Pirker; Andrew M Donson; Peter Bannauer; Pia Korbel; Carola N Jaunecker; Jens-Martin Hübner; Lisa Mayr; Sibylle Madlener; Maria T Schmook; Gerda Ricken; Kendra Maaß; Michael Grusch; Klaus Holzmann; Bettina Grasl-Kraupp; Sabine Spiegl-Kreinecker; Jennifer Hsu; Christian Dorfer; Karl Rössler; Amedeo A Azizi; Nicholas K Foreman; Andreas Peyrl; Christine Haberler; Thomas Czech; Irene Slavc; Mariella G Filbin; Kristian W Pajtler; Marcel Kool
Journal:  Acta Neuropathol       Date:  2021-05-27       Impact factor: 17.088

  2 in total

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