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Update on Chemotherapeutic Approaches and Management of Bevacizumab Usage for Glioblastoma

机译:胶质母细胞瘤的化学治疗方法及北伐木人用法的更新

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摘要

Glioblastoma, the most common primary brain tumor in adults, has one of the most dismal prognoses in cancer. In 2009, bevacizumab was approved for recurrent glioblastoma in the USA. To evaluate the clinical impact of bevacizumab as a first-line drug for glioblastoma, two randomized clinical trials, AVAglio and RTOG 0825, were performed. Bevacizumab was found to improve progression-free survival (PFS) and was reported to be beneficial for maintaining patient performance status as an initial treatment. These outcomes led to bevacizumab approval in Japan in 2013 as an insurance-covered first-line drug for glioblastoma concurrently with its second-line application. However, prolongation of overall survival was not evinced in these clinical trials; hence, the clinical benefit of bevacizumab for newly diagnosed glioblastomas remains controversial. A recent meta-analysis of randomized controlled trials of bevacizumab combined with temozolomide in recurrent glioblastoma also showed an effect only on PFS, and the benefit of bevacizumab even for recurrent glioblastoma is controversial. Here, we discuss the clinical impact of bevacizumab for glioblastoma treatment by reviewing previous clinical trials and real-world evidence by focusing on Japanese experiences. Moreover, the efficacy and safety of bevacizumab are summarized, and we provide suggestions for updating the approaches and management of bevacizumab.
机译:胶质母细胞瘤,成人中最常见的主要脑肿瘤,具有癌症中最令人沮丧的预期之一。 2009年,Bevacizumab在美国批准用于复发胶质母细胞瘤。为了评估Bevacizumab作为胶质母细胞瘤的一线药物的临床影响,进行了两种随机临床试验,AVAGLIO和RTOG 0825。发现Bevacizumab改善了无进展的生存(PFS),并据报道,有利于将患者性能状况保持为初始治疗。这些结果导致2013年日本的Bevacizumab批准,作为胶质母细胞瘤的保险覆盖的一线药物,其二线申请表同时。然而,在这些临床试验中,整体存活的延长并不表达;因此,Bevacizumab对新诊断的胶质细胞瘤的临床益处仍存在争议。最近对贝伐单抗的随机对照试验结合替代胶质母细胞瘤中的随机对照试验也表现出仅对PFS的影响,并且贝伐单抗甚至用于复发性胶质母细胞瘤的益处是有争议的。在这里,我们通过专注于日本经验,讨论贝伐单抗治疗味肌瘤治疗的临床影响。此外,总结了Bevacizumab的功效和安全性,我们提供了更新Bevacizumab的方法和管理的建议。

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