Rindopepimut:对其治疗egfrviii阳性胶质母细胞瘤潜力的循证评价

Core Evidence Pub Date : 2012-01-01 Epub Date: 2012-09-14 DOI:10.2147/CE.S29001
Ranjith Babu, D Cory Adamson
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引用次数: 54

摘要

多形性胶质母细胞瘤(GBM)是成人最常见的原发性脑肿瘤,具有普遍的致命性。尽管手术切除,放疗和全身化疗,中位总生存期小于15个月。由于目前的治疗方法不是肿瘤特异性的,治疗通常会导致毒性。表皮生长因子受体变体III (EGFRvIII)是一种自然发生的EGFR突变体,在约20%至30%的GBMs中表达。由于它不在正常细胞上表达,因此是一种理想的治疗靶点。Rindopepimut是一种肽疫苗,可引起egfrviii特异性体液和细胞免疫反应。I期和II期临床试验表明,接种egfrviii表达的GBM肿瘤患者的无进展期和总生存期显着提高。副作用很小,主要是过敏反应。由于rindopepimut的有效性和安全性,它是治疗GBM患者的一种很有希望的治疗方法。目前,rindopepimut正在一项针对新诊断GBM的国际III期试验和一项针对复发GBM的II期试验中进行临床试验。
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Rindopepimut: an evidence-based review of its therapeutic potential in the treatment of EGFRvIII-positive glioblastoma.

Glioblastoma multiforme (GBM) is the most common primary brain tumor in adults and is universally fatal. Despite surgical resection, radiotherapy, and systemic chemotherapy, the median overall survival is less than 15 months. As current therapies are not tumor-specific, treatment commonly results in toxicity. The epidermal growth factor receptor variant III (EGFRvIII) is a naturally occurring mutant of EGFR and is expressed on approximately 20% to 30% of GBMs. As it is not expressed on normal cells, it is an ideal therapeutic target. Rindopepimut is a peptide vaccine which elicits EGFRvIII-specific humoral and cellular immune responses. Phase I and II clinical trials have demonstrated significantly higher progression-free and overall survival times in vaccinated patients with EGFRvIII-expressing GBM tumors. Side effects are minimal and mainly consist of hypersensitivity reactions. Due to the efficacy and safety of rindopepimut, it is a promising therapy for patients with GBM. Currently, rindopepimut is undergoing clinical testing in an international Phase III trial for newly diagnosed GBM and a Phase II trial for relapsed GBM.

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Core Evidence
Core Evidence PHARMACOLOGY & PHARMACY-
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期刊介绍: Core Evidence evaluates the evidence underlying the potential place in therapy of drugs throughout their development lifecycle from preclinical to postlaunch. The focus of each review is to evaluate the case for a new drug or class in outcome terms in specific indications and patient groups The emerging evidence on new drugs is reviewed at key stages of development and evaluated against unmet needs
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