Riethmüller G, Schneider-Gädicke E, Schlimok G, Schmiegel W, Raab R, Höffken K, Gruber R, Pichlmaier H, Hirche H, Pichlmayr R
Institut für Immunologie, Ludwig-Maximillans-Universität München, Germany.
Lancet. 1994 May 14;343(8907):1177-83. doi: 10.1016/s0140-6736(94)92398-1.
Over the past decade various clinical trials have used monoclonal antibodies as therapeutic agents against solid tumours. No consistent pattern of response or improved survival has yet emerged although antigenic heterogeneity and insufficient accessibility of cells in advanced tumours have been offered as explanations for these failures. We designed a study in which a monoclonal antibody was used to target minimal residual disease in an early stage of tumour cell dissemination in patients with colorectal cancer. Only patients in Dukes' stage C who had undergone curative surgery and were free of manifest residual tumour were admitted. 189 patients with colorectal cancer of stage Dukes' C were randomly assigned to an observation regimen or to postoperative treatment with 500 mg of 17-1A antibody, followed by four 100 mg infusions each month. A balance of risk factors in the two groups was achieved by dynamic randomisation procedure. After a median follow-up of 5 years, antibody treatment reduced the overall death rate by 30% (Cox's proportional hazard, p = 0.04, log-rank p = 0.05) and decreased the recurrence rate by 27% (p = 0.03, p = 0.05). The effect of antibody was most pronounced in patients who had distant metastasis as first sign of a relapse (p = 0.0014, p = 0.002), an effect that was not seen for local relapses (p = 0.74, p = 0.67). Toxic effects of 17-1A antibody were infrequent, consisting mainly of mild constitutional and gastrointestinal symptoms. During 371 infusions four anaphylactic reactions were seen, all controllable by intravenous steroids and none necessitated admission to hospital. Adjuvant therapy with 17-1A antibody extends life and prolongs remission in patients with colorectal cancer of Dukes' stage C.
在过去十年中,各种临床试验都将单克隆抗体用作治疗实体瘤的药物。尽管有人认为抗原异质性和晚期肿瘤中细胞的可及性不足是这些试验失败的原因,但目前尚未出现一致的反应模式或生存率提高的情况。我们设计了一项研究,在结直肠癌患者肿瘤细胞播散的早期阶段,使用单克隆抗体靶向微小残留病灶。仅纳入了处于Dukes C期且已接受根治性手术且无明显残留肿瘤的患者。189例Dukes C期结直肠癌患者被随机分配至观察方案组或术后接受500 mg 17-1A抗体治疗组,随后每月进行4次100 mg静脉输注。通过动态随机程序实现了两组危险因素的平衡。中位随访5年后,抗体治疗使总死亡率降低了30%(Cox比例风险,p = 0.04,对数秩检验p = 0.05),复发率降低了27%(p = 0.03,p = 0.05)。抗体的效果在以远处转移作为复发首发征象的患者中最为显著(p = 0.0014,p = 0.002),而局部复发患者未观察到这种效果(p = 0.74,p = 0.67)。17-1A抗体的毒性反应很少见,主要包括轻微的全身症状和胃肠道症状。在371次输注过程中,出现了4次过敏反应,均可用静脉类固醇控制,无一例需要住院治疗。17-1A抗体辅助治疗可延长Dukes C期结直肠癌患者的生命并延长缓解期。