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Treatment of high-grade glioma patients with the humanized anti-epidermal growth factor receptor (EGFR) antibody h-R3: report from a phase I/II trial.

机译:使用人源化抗表皮生长因子受体(EGFR)抗体h-R3治疗高级神经胶质瘤患者:I / II期试验报告。

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The poor prognosis of patients with high-grade glioma has led to the search for new therapeutic strategies. More than half of these tumors overexpress Epidermal Growth factor Receptor (EGFR). h-R3 is a humanized monoclonal antibody that recognize the EGFR external domain with high affinity, inhibiting tyrosine kinase activation. In order to evaluate safety, immunogenicity and preliminary efficacy of h-R3 in newly diagnosed high-grade glioma patients, we conducted a Phase I/II trial. Patients received six weekly infusions of h-R3 at the dose of 200 mg in combination with external beam radiotherapy. Twenty-nine patients (mean age, 45 years and median KPS 80) were entered into the study. Tumor types were: glioblastoma (GB) (16 patients), anaplastic astrocytoma (AA) (12 patients) and anaplastic oligodendroglioma (AO) (1 patient). All patients underwent debulking surgery or biopsy before entering the trial. The antibody was very well tolerated. No evidences of grade 3/4 adverse events were detected. None ofthe patients developed acneiform rash or allergic reactions. One patient developed a positive anti-idiotypic response. Objective response-rate was 37.9% (17.2% complete response, 20.7% partial response) while stable disease occurred in 41.4% of the patients. With a median follow up time of 29 months, the median survival is 22.17 months for all subjects. Median survival time (MST) is 17.47 months for GB, whereas MST is not reached for AA patients.
机译:高度脑胶质瘤患者预后较差,因此寻求新的治疗策略。这些肿瘤中有一半以上过表达表皮生长因子受体(EGFR)。 h-R3是一种人源化单克隆抗体,可以高亲和力识别EGFR外部结构域,从而抑制酪氨酸激酶的活化。为了评估h-R3在新诊断的高级别神经胶质瘤患者中的安全性,免疫原性和初步疗效,我们进行了I / II期试验。患者接受六次每周200毫克剂量的h-R3输注并结合外照射治疗。 29名患者(平均年龄,45岁和中位数KPS为80)进入了研究。肿瘤类型为:胶质母细胞瘤(GB)(16例),间变性星形细胞瘤(AA)(12例)和间变性少突胶质细胞瘤(AO)(1例)。所有患者在进入试验之前均接受了减瘤手术或活检。该抗体具有很好的耐受性。没有发现3/4级不良事件的证据。没有患者出现痤疮样皮疹或过敏反应。一名患者出现了积极的抗独特型反应。客观缓解率为37.9%(完全缓解为17.2%,部分缓解为20.7%),而稳定疾病的发生率为41.4%。中位随访时间为29个月,所有受试者的中位生存期为22.17个月。 GB的中位生存时间(MST)为17.47个月,而AA患者未达到MST。

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