Rindopepimut, a 14-mer injectable peptide vaccine against EGFRvIII for the potential treatment of glioblastoma multiforme.

Catherine A Del Vecchio, Albert J Wong
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Abstract

Celldex Therapeutics is developing rindopepimut (CDX-110), a 14-mer injectable peptide vaccine for the potential treatment of glioblastoma multiforme (GBM). Rindopepimut specifically targets a novel junctional epitope of the EGFR deletion mutant EGFRvIII, which is a constitutively active receptor that is expressed in approximately 60 to 70% of patients with GBM. EGFRvIII expression is correlated with worse prognosis and reduced overall survival. Importantly, EGFRvIII is not expressed in normal brain tissue, making it an excellent therapeutic target. Preclinical studies demonstrated lasting tumor regression and increased survival times, as well as efficient generation of EGFRvIII-specific humoral and cellular immune responses, in animals expressing EGFRvIII and vaccinated with rindopepimut. Phase I and II clinical trials in patients with GBM demonstrated significantly increased median time to progression and overall survival time in those vaccinated with rindopepimut compared with matched historical controls. Only limited side effects have been observed in patients. Given these results, rindopepimut is an extremely promising therapy for patients with GBM. Phase I and II clinical trials in patients with GBM were ongoing at the time of publication. In the future, it may be beneficial to combine rindopepimut with other treatment modalities to further prolong survival.

Rindopepimut,一种针对EGFRvIII的14分子注射肽疫苗,可用于多形性胶质母细胞瘤的潜在治疗。
Celldex Therapeutics正在开发rindopepimut (CDX-110),这是一种14分子可注射肽疫苗,可用于多形性胶质母细胞瘤(GBM)的潜在治疗。Rindopepimut特异性靶向EGFR缺失突变体EGFRvIII的一种新的连接表位,EGFRvIII是一种组成型活性受体,在大约60%至70%的GBM患者中表达。EGFRvIII表达与预后不良和总生存期降低相关。重要的是,EGFRvIII在正常脑组织中不表达,使其成为一个很好的治疗靶点。临床前研究表明,在表达EGFRvIII并接种rindopepimut的动物中,肿瘤持续消退,生存时间延长,以及EGFRvIII特异性体液和细胞免疫反应的有效产生。GBM患者的I期和II期临床试验表明,与匹配的历史对照组相比,接种rindopepimut的患者的中位进展时间和总生存时间显着增加。在患者中只观察到有限的副作用。鉴于这些结果,rindopepimut对GBM患者是一种极有希望的治疗方法。在本文发表时,GBM患者的I期和II期临床试验正在进行中。在未来,rindopepimut与其他治疗方式联合使用可能有利于进一步延长生存期。
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来源期刊
Current Opinion in Molecular Therapeutics
Current Opinion in Molecular Therapeutics 医学-生物工程与应用微生物
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