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静脉注射双特异性单克隆抗体OC/TR F(ab')2在卵巢癌患者中的药代动力学、生物分布及生物学效应

Pharmacokinetics, biodistribution and biological effects of intravenously administered bispecific monoclonal antibody OC/TR F(ab')2 in ovarian carcinoma patients.

作者信息

Tibben J G, Boerman O C, Massuger L F, Schijf C P, Claessens R A, Corstens F H

机构信息

Department of Obstetrics and Gynaecology, University Hospital Nijmegen St. Radboud, The Netherlands.

出版信息

Int J Cancer. 1996 May 16;66(4):477-83. doi: 10.1002/(SICI)1097-0215(19960516)66:4<477::AID-IJC11>3.0.CO;2-5.

Abstract

The bispecific monoclonal antibody (biMAb) OC/TR combines the anti-ovarian-cancer reactivity of the MOv18 monoclonal antibody (MAb) with the reactivity of an anti-CD3 MAb. Pre-clinical studies have indicated that this biMAb is able to redirect the cytolytic activity of T cells towards tumour cells, resulting in efficient tumour-cell lysis. To assess the clinical potential of systemic biMAb-based cancer therapy we initiated a study in ovarian-cancer patients. Five patients suspected of ovarian cancer received 123I-OC/TR F(ab')2 i.v. Unexpectedly, the first patient developed side effects (grade III-IV toxicity) starting 30 min after infusion (p.i.) of 1 mg of OC/TR F(ab')2. After approval of the Ethical Committee, the study was continued at lower dose levels (0.1 mg; 0.2 mg). However, at the 0.2-mg dose level similar side effects were observed. FACS analysis indicated that all peripheral T cells were coated with biMAb immediately following the infusion. The cytokines tumour necrosis factor-alpha, interferon-gamma and interleukin-2 showed maximum serum concentrations 2 h p.i. Tumour uptake ranged from 0.8 to 1.9% ID/kg, resulting in tumour/background ratios of 3 to 8. Our results suggest that at higher antibody dose levels OC/TR F(ab')2 causes T-cell activation with acute release of cytokines. Only low doses of biMAb can be administered safely. Despite the interaction with T cells, OC/TR F(ab')2 preferentially localizes in tumours following i.v. administration, thus offering therapeutic perspectives.

摘要

双特异性单克隆抗体(biMAb)OC/TR将MOv18单克隆抗体(MAb)的抗卵巢癌反应性与抗CD3 MAb的反应性结合在一起。临床前研究表明,这种双特异性单克隆抗体能够将T细胞的细胞溶解活性重定向至肿瘤细胞,从而实现高效的肿瘤细胞裂解。为了评估基于双特异性单克隆抗体的全身性癌症治疗的临床潜力,我们启动了一项针对卵巢癌患者的研究。5名疑似卵巢癌的患者静脉注射了123I-OC/TR F(ab')2。出乎意料的是,第一名患者在静脉注射1 mg OC/TR F(ab')2后30分钟开始出现副作用(III-IV级毒性)。经伦理委员会批准后,该研究在较低剂量水平(0.1 mg;0.2 mg)继续进行。然而,在0.2 mg剂量水平观察到了类似的副作用。流式细胞术分析表明,输注后所有外周血T细胞立即被双特异性单克隆抗体包被。细胞因子肿瘤坏死因子-α、干扰素-γ和白细胞介素-2在输注后第2小时显示出血清浓度峰值。肿瘤摄取率为0.8%至1.9% ID/kg,肿瘤/背景比值为3至8。我们的结果表明,在较高抗体剂量水平下,OC/TR F(ab')2会导致T细胞活化并伴有细胞因子的急性释放。只能安全地给予低剂量的双特异性单克隆抗体。尽管与T细胞相互作用,但静脉注射后OC/TR F(ab')2优先定位于肿瘤中,因此具有治疗前景。

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