| Literature DB >> 30616755 |
Luiz Henrique Medeiros Geraldo1, Celina Garcia2, Anna Carolina Carvalho da Fonseca2, Luiz Gustavo Feijó Dubois3, Tânia Cristina Leite de Sampaio E Spohr3, Diana Matias4, Eduardo Sabino de Camargo Magalhães2, Rackele Ferreira do Amaral2, Barbara Gomes da Rosa5, Izabella Grimaldi2, Felipe Sceanu Leser2, José Marcos Janeiro2, Lucy Macharia3, Caroline Wanjiru3, Claudia Maria Pereira6, Vivaldo Moura-Neto7, Catarina Freitas8, Flavia Regina Souza Lima9.
Abstract
Glioblastoma (GBM) is the most common and fatal primary malignant brain tumor. Despite advances in the understanding of the biology of gliomas, little has changed in the treatment of these tumors in the past decade. Phase III clinical trials showed no benefit for the use of bevacizumab in newly diagnosed patients, leading to a renewed search for new antiangiogenic drugs, as well as immunotherapeutic approaches, including checkpoint inhibitors, chimeric antigen receptor T cells, and intracerebral CpG-oligodeoxynucleotides. The emerging role of infiltrating microglia and macrophages, and of metabolic alterations, is also being taken into account in preclinical research and drug development. In this review, we discuss progress in the search for new therapeutic strategies, particularly approaches focusing on the tumor microenvironment.Entities:
Keywords: angiogenesis; cancer metabolism; cancer therapy; glioblastoma; immunotherapy; microglia
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Year: 2018 PMID: 30616755 DOI: 10.1016/j.trecan.2018.11.002
Source DB: PubMed Journal: Trends Cancer ISSN: 2405-8025