Stephen E. and Catherine Pappas Center for Neuro-Oncology, Boston, MA 02114, USA.
Nat Rev Clin Oncol. 2013 Jan;10(1):14-26. doi: 10.1038/nrclinonc.2012.204. Epub 2012 Nov 27.
Glioblastomas are heterogeneous neoplasms that are driven by complex signalling pathways, and are among the most aggressive and challenging cancers to treat. Despite standard treatment with resection, radiation and chemotherapy, the prognosis of patients with glioblastomas remains poor. An increasing understanding of the molecular pathogenesis of glioblastomas has stimulated the development of novel therapies, including the use of molecular-targeted agents. Identification and validation of diagnostic, prognostic and predictive biomarkers has led to the advancement of clinical trial design, and identification of glioblastoma subgroups with a more-favourable prognosis and response to therapy. In this Review, we discuss common molecular alterations relevant to the biology of glioblastomas, targeted, antiangiogenic and immunotherapies that have impacted on the treatment of this disease, and the challenges and pitfalls associated with these therapies. In addition, we emphasize current biomarkers relevant to the management of patients with glioblastoma.
胶质母细胞瘤是由复杂信号通路驱动的异质性肿瘤,是治疗最具侵袭性和挑战性的癌症之一。尽管采用标准的手术切除、放疗和化疗进行治疗,但胶质母细胞瘤患者的预后仍然较差。对胶质母细胞瘤分子发病机制的认识不断加深,刺激了新型治疗方法的发展,包括使用分子靶向药物。诊断、预后和预测生物标志物的鉴定和验证促进了临床试验设计的发展,并确定了具有更好预后和对治疗反应的胶质母细胞瘤亚组。在这篇综述中,我们讨论了与胶质母细胞瘤生物学相关的常见分子改变、靶向、抗血管生成和免疫疗法,这些疗法影响了这种疾病的治疗,并且还强调了与这些疗法相关的挑战和陷阱。此外,我们还强调了与胶质母细胞瘤患者管理相关的当前生物标志物。