贝伐单抗
胶质母细胞瘤
小胶质细胞
医学
胶质瘤
临床试验
免疫疗法
肿瘤微环境
癌症研究
脑瘤
肿瘤科
癌症
免疫学
内科学
病理
化疗
炎症
作者
Luiz Henrique Geraldo,Celina García,Anna Carolina Carvalho da Fonseca,Luiz Gustavo Dubois,Tânia Cristina Leite de Sampaio e Spohr,Diana Matias,Eduardo Sabino de Camargo Magalhães,Rackele Ferreira do Amaral,Bárbara Gomes da Rosa,Izabella Grimaldi,Felipe Saceanu Leser,José Marcos Janeiro,Lucy Wanjiku Macharia,Caroline M. Wanjiru,Cláudia Maria Pereira,Vivaldo Moura‐Neto,Catarina Freitas,Flávia Regina Souza Lima
标识
DOI:10.1016/j.trecan.2018.11.002
摘要
Glioblastoma remains an incurable disease with a poor prognosis, despite being among the most studied tumors in the past decade. About a third of the tumor mass is composed of non-neoplasic infiltrating cells, reflecting a very heterogeneous tumor both in terms of pathology and microenvironment. The heterogeneous microenvironment makes glioblastoma a good candidate for cellular therapy and immunotherapies. But it also constitutes a challenge for interpreting treatment response and developing new strategies. 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. 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.
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