Cheung N K, Lazarus H, Miraldi F D, Abramowsky C R, Kallick S, Saarinen U M, Spitzer T, Strandjord S E, Coccia P F, Berger N A
J Clin Oncol. 1987 Sep;5(9):1430-40. doi: 10.1200/JCO.1987.5.9.1430.
The murine IgG3 monoclonal antibody (MoAb) 3F8, specific for the ganglioside GD2, activates human complement, is active in antibody-dependent cell-mediated cytotoxicity (ADCC), and can target specifically to human neuroblastoma in patients with metastatic disease. In a phase I study, 3F8 was administered intravenously (IV) to 17 patients with metastatic GD2 positive neuroblastoma or malignant melanoma at doses of 5, 20, 50, and 100 mg/m2. Serum 3F8 levels achieved were proportional to the dose of 3F8 infused. However, serum antimouse antibody levels did not increase with the amount of 3F8 administered. Toxicities included pain, hypertension, urticaria, and complement depletion. All acute side effects were controllable with symptomatic therapy. No long-term side effects were detected in patients observed for more than 14 months. None of the 17 patients received any antitumor therapy postantibody treatment. Antitumor responses occurred in seven of 17 patients. These ranged from complete clinical remissions to mixed responses. The murine monoclonal antibody (MoAb) 3F8 has clinical utility for the diagnosis and therapy of neuroblastoma and melanoma.
针对神经节苷脂GD2的鼠源IgG3单克隆抗体(MoAb)3F8可激活人补体,在抗体依赖性细胞介导的细胞毒性(ADCC)中具有活性,并且能够特异性靶向转移性疾病患者的人神经母细胞瘤。在一项I期研究中,对17例转移性GD2阳性神经母细胞瘤或恶性黑色素瘤患者静脉注射(IV)3F8,剂量分别为5、20、50和100mg/m²。所达到的血清3F8水平与输注的3F8剂量成正比。然而,血清抗鼠抗体水平并未随着3F8给药量的增加而升高。毒性反应包括疼痛、高血压、荨麻疹和补体耗竭。所有急性副作用均可通过对症治疗得到控制。在观察超过14个月的患者中未检测到长期副作用。17例患者中无一例在抗体治疗后接受任何抗肿瘤治疗。17例患者中有7例出现抗肿瘤反应。这些反应范围从完全临床缓解到混合反应。鼠源单克隆抗体(MoAb)3F8在神经母细胞瘤和黑色素瘤的诊断和治疗中具有临床应用价值。