Maxwell-Armstrong C A, Durrant L G, Buckley T J, Scholefield J H, Robins R A, Fielding K, Monson J R, Guillou P, Calvert H, Carmichael J, Hardcastle J D
Division of Gastrointestinal Surgery, University Hospital, Queens Medical Centre, Nottingham, NG7 2UH, UK.
Br J Cancer. 2001 Jun 1;84(11):1443-6. doi: 10.1054/bjoc.2001.1725.
The cancer vaccine 105AD7 is an anti-idiotypic monoclonal antibody that mimics the tumour-associated antigen 791T/gp72 (CD55, Decay Accelerating Factor) on colorectal cancer cells. Phase I studies in patients with advanced disease confirmed that 105AD7 is non-toxic, and that T cell responses could be generated. A prospective, randomized, double-blind, placebo-controlled survival study in patients with advanced colorectal cancer was performed. 162 patients were enrolled between April 1994 and October 1996. Patients attended at trial entry, and at 6 and 12 weeks, where they received 105AD7 or placebo. Study groups were comparable in terms of patient demographics, and time from diagnosis of advanced colorectal cancer (277.1 v 278.6 days). Baseline disease was similar, with 50% of patients having malignancy in at least 2 anatomic sites. Compliance with treatment was poor, with only 50% of patients receiving 3 planned vaccinations. Median survival from randomization date was 124 and 184 days in 105AD7 and placebo arms respectively (P = 0.38), and 456 and 486 days from the date of diagnosis of advanced disease (P = 0.82). 105AD7 vaccination does not prolong survival in patients with advanced colorectal cancer. The reasons for lack of efficacy are unclear, but may reflect the high tumour burden in the patient population, and poor compliance with immunization. Further vaccine studies should concentrate on patients with minimal residual disease.
癌症疫苗105AD7是一种抗独特型单克隆抗体,可模拟结肠直肠癌细胞上的肿瘤相关抗原791T/gp72(CD55,衰变加速因子)。针对晚期疾病患者的I期研究证实,105AD7无毒,且可产生T细胞应答。对晚期结肠直肠癌患者进行了一项前瞻性、随机、双盲、安慰剂对照的生存研究。1994年4月至1996年10月期间招募了162例患者。患者在试验入组时、6周和12周时就诊,分别接受105AD7或安慰剂。研究组在患者人口统计学以及从晚期结肠直肠癌诊断算起的时间方面(277.1天对278.6天)具有可比性。基线疾病相似,50%的患者在至少2个解剖部位存在恶性肿瘤。治疗依从性较差,只有50%的患者接受了3次计划接种。从随机分组日期起,105AD7组和安慰剂组的中位生存期分别为124天和184天(P = 0.38),从晚期疾病诊断日期起分别为456天和486天(P = 0.82)。105AD7疫苗接种不能延长晚期结肠直肠癌患者的生存期。疗效欠佳的原因尚不清楚,但可能反映了患者群体中肿瘤负荷较高以及免疫接种依从性较差。进一步的疫苗研究应集中于残留疾病极少的患者。