| Literature DB >> 33320972 |
Antonella Cacchione1, Mariachiara Lodi1, Andrea Carai2, Evelina Miele1, Marco Tartaglia3, Giacomina Megaro1, Giada Del Baldo1, Iside Alessi1, Giovanna Stefania Colafati4, Alessia Carboni4, Luigi Boccuto5,6, Francesca Diomedi Camassei7, Giuseppina Catanzaro8, Agnese Po9, Elisabetta Ferretti8, Lucia Pedace1, Simone Pizzi3, Valentina Folgiero1, Marco Pezzullo10, Tiziana Corsetti11, Domitilla Elena Secco12, Maria Giuseppina Cefalo1, Franco Locatelli1,13, Angela Mastronuzzi1.
Abstract
Pediatric low-grade gliomas (pLGGs) are the most frequent brain tumor in children. Adjuvant treatment, consisting in chemotherapy and radiotherapy, is often necessary if a complete surgical resection cannot be obtained. Traditional treatment approaches result in a significant long-term morbidity, with a detrimental impact on quality of life. Dysregulation of the mitogen-activated protein kinase (MAPK) pathway is the molecular hallmark of pLGGs and hyper-activation of the downstream mammalian target of rapamycin (mTOR) pathway is frequently observed. We report clinical and radiological results of front-line treatment with everolimus in 10 consecutive patients diagnosed with m-TOR positive pLGGs at the Bambino Gesù Children's Hospital in Rome, Italy. Median duration of treatment was 19 months (range from 13-60). Brain magnetic resonance imaging showed stable disease in 7 patients, partial response in 1 and disease progression in 2. Therapy-related adverse events were always reversible after dose reduction or temporary treatment interruption. To the best of our knowledge, this is the first report of everolimus treatment for chemo- and radiotherapy-naïve children with pLGG. Our results provide preliminary support, despite low samples size, for the use of everolimus as target therapy in pLGG showing lack of progression with a manageable toxicity profile. This article is protected by copyright. All rights reserved.Entities:
Keywords: MAPK pathway; everolimus; mTOR; pediatric low-grade gliomas
Year: 2020 PMID: 33320972 DOI: 10.1002/ijc.33438
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396