抗表皮生长因子受体中和性单克隆抗体在晚期脑肿瘤患者中的I期临床评价:初步研究。

T. Crombet, O. Torres, V. Rodríguez, A. Menendez, A. Stevenson, M. Ramos, F. Torres, R. Figueredo, I. Veitia, N. Iznaga, R. Pérez, A. Lage
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引用次数: 61

摘要

高水平的生长因子及其受体已在人类肿瘤中得到证实。胶质瘤和脑膜瘤以表皮生长因子受体(EGF-R)过表达为特征。Ior egf/r3是一种针对egf - r的中和性小鼠单克隆抗体(MAb),由古巴肿瘤研究所产生。该抗体以高亲和力识别EGF-R,抑制酪氨酸激酶的激活。在脑肿瘤患者中进行了一项临床试验,以评估不断增加剂量的抗体的毒性、免疫原性和临床益处。9例经组织学证实的胶质瘤或脑膜瘤患者,在接受常规治疗后出现活动性或复发性疾病,接受了4次静脉注射剂量的ior egf/r3。总剂量为160至480毫克。作为纳入标准,使用99mTechnetium (99mTc)标记的同一单抗进行放射免疫显像。对小鼠抗体的免疫反应也进行了评价。在四次剂量的ior egf/r3单抗治疗后,除一名患者出现4级过敏性不良事件外,未发现明显的毒性。这种反应可能与先前对同一单抗的致敏和人抗小鼠抗体(HAMA)反应的发展有关。尽管没有主要的客观抗肿瘤反应,8例患者在6个月的评估中病情稳定,2例患者在接受4年单克隆抗体治疗后仍然存活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phase I clinical evaluation of a neutralizing monoclonal antibody against epidermal growth factor receptor in advanced brain tumor patients: preliminary study.
High levels of growth factors and their receptors have been demonstrated in human tumors. Gliomas and meningiomas are characterized by overexpression of epidermal growth factor receptor (EGF-R). Ior egf/r3, is a neutralizing murine monoclonal antibody (MAb) against EGF-R, and was generated at the Cuban Institute of Oncology. The antibody recognizes EGF-R with high affinity, inhibiting tyrosine kinase activation. A clinical trial was conducted in brain tumor patients to evaluate toxicity, immunogenicity, and clinical benefit of escalating doses of the antibody. Nine patients with histologically confirmed gliomas or meningiomas, who had active or recurrent disease after receiving conventional treatment, received four intravenous doses of ior egf/r3. Total dosages ranged from 160 to 480 mg. As inclusion criteria, radioimmunoscintigraphy with the same MAb labeled with 99mTechnetium (99mTc) was performed. Immune response against the murine antibody was also evaluated. After four doses of ior egf/r3 MAb, no significant toxicity was found, except in one patient who developed a grade 4 allergic adverse event. This reaction was probably related with previous sensitization to the same MAb and the development of human anti-mouse antibodies (HAMA) response. Despite no major objective antitumor responses, eight patients had stable disease on the 6-month evaluation, and two patients remain alive after four years of MAb therapy.
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来源期刊
Hybridoma
Hybridoma 医学-免疫学
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