Therapeutic approach beyond conventional temozolomide for newly diagnosed glioblastoma: Review of the present evidence and future direction.

Supriya Mallick, Ajeet Kumar Gandhi, Goura Kishor Rath
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Abstract

Glioblastoma multiforme (GBM) is the most aggressive form of primary brain tumor. Maximal safe surgical resection followed by adjuvant partial brain radiation with concurrent and adjuvant temozolomide (TMZ) (oral alkylating agent) is the standard of care. Five years survival in TMZ treated patient reaches 9.8%. We aimed to summarize the changes in the management of GBM beyond conventional temozolomide based adjuvant treatment. We searched the PUBMED with the following key words: Glioblastoma, phase III trial, Phase II trial, adjuvant treatment in GBM. Clinical research has found a wide range of molecular aberrations in GBM and attempts are being made to further improve survival with the addition of different classes of drugs. Angiogenesis inhibitors, oncolytic vaccines, dose dense TMZ, and anti-epidermal growth factor receptor monoclonal antibody in phase III trials have failed to improve survival. Recent studies have also shown that the management strategies might be different and needs to be customized as per the age of patients such as pediatric and elderly patients. In addition, treatments should be personalized depending on the molecular aberrations. We reviewed all published phase III trials for newly diagnosed GBM as well as also looked into possible future directions in this review. Limited progress has happed beyond conventional TMZ in the adjuvant treatment of GBM. Newer insights are emerging about treatment intensification and introduction of newer molecular targeted drugs with more information about molecular aberrations.

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新诊断胶质母细胞瘤的常规替莫唑胺以外的治疗方法:现有证据回顾与未来方向。
多形性胶质母细胞瘤(GBM)是侵袭性最强的原发性脑肿瘤。目前的标准治疗方法是进行最安全的手术切除,然后进行部分脑部放射治疗,并同时辅助替莫唑胺(TMZ)(口服烷化剂)。接受替莫唑胺治疗的患者五年生存率达到 9.8%。我们的目的是总结在以替莫唑胺为基础的传统辅助治疗之外,GBM 的治疗方法发生了哪些变化。我们用以下关键词在 PUBMED 上进行了搜索:胶质母细胞瘤、III 期试验、II 期试验、GBM 的辅助治疗。临床研究发现,胶质母细胞瘤存在多种分子畸变,目前正试图通过添加不同类别的药物来进一步提高生存率。在 III 期试验中,血管生成抑制剂、肿瘤溶解疫苗、剂量密集的 TMZ 和抗表皮生长因子受体单克隆抗体都未能提高生存率。最近的研究还表明,治疗策略可能有所不同,需要根据患者的年龄(如儿童和老年患者)量身定制。此外,还应根据分子畸变情况采取个性化治疗。在本综述中,我们回顾了所有已发表的针对新诊断 GBM 的 III 期试验,并探讨了未来可能的发展方向。在 GBM 的辅助治疗方面,除了传统的 TMZ 之外,取得的进展有限。随着分子畸变信息的增多,关于强化治疗和引入新型分子靶向药物的新见解也在不断涌现。
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Gray Matter Alterations in Panic Disorder: A Voxel-Wise Meta-Analysis. Therapeutic approach beyond conventional temozolomide for newly diagnosed glioblastoma: Review of the present evidence and future direction. Foreword Preface Technology Assessment for the Anesthesiologist
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