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作 者:吴英德[1,2] 周德南[1,2] 甘友全[1,2] 胡晓桦[1,2] 李志革[1,2] 宋向群[1,2] 贺海平[1,2] 杨克政[1,2] 黄秉琰[1,2]
机构地区:[1]广西医科大学附属肿瘤医院化疗科 [2]广西肿瘤防治研究所
出 处:《新消化病学杂志》1997年第7期415-416,共2页
基 金:国家八五科技攻关基金
摘 要:目的观察化疗兼内照射的新型双弹头免疫导向治疗肝癌的疗效.方法以马抗人AFP多克隆抗体(抗AFPAb)和大鼠抗人AFP单克隆抗体(抗AFPMcAb)为载体,核素131I和丝裂霉素(MMC)为双弹头,采用改良氯胺T法制备131I抗AFPMcAbMMC(双弹头1)和131I抗AFPAbMMC(双弹头2),静脉滴注,每月1次,治疗不能切除中晚肝癌31例(治疗组).治疗1,2,3次分别占4,17和10例,放射剂量(MBq/例)均值依次为19351±3774,6519±2324和9920±2305.结果治后肿瘤缩小率、血清AFP下降率和1,2年生存率分别高于同期经动脉插管灌注(TAI)或化疗栓塞(TACE)的对照组(500%,15/30比300%,9/30P<005;667%,18/27比280%,7/25P<001和500%比330%,340%比33%P<001),治疗组病例的进展率(100%)明显低于对照组(400%,P<001).结论双弹头疗效提高,由于抗体、核素131I和抗癌药的协同作用而增强了对癌细胞的杀伤力所致.AIM To observe the effect of a double bullet immunotargeting therapy with the merit of chemotherapy and internal radiotherapy for primary liver cancer. METHODS The polyclonal horse antibody against human AFP (anti AFPAb) and the monoclonal murine antibody against human AFP (anti AFPMcAb) were used as carriers, and 131 I and mitomycin C (MMC) as warheads, to form double bullet, ie, 131 I anti AFPMcAb MMC (double bullet 1) and 131 I anti AFPAb MMC (double bullet 2) prepared by the modified chloramine T method. The double bullet targeting therapy was administered by intravenous drip once a month in 31 patients (treatment group) with unresectable primary liver cancer. Among them 4, 17 and 10 patients were administered 1, 2 and 3 times, and the median value of radiation dose (MBq/case) were 193 5±37 74; 651 9±232 4, and 992 0±230 5 respectively. RESULTS The shrinkage of tumor, AFP decrease and 1 and 2 year survival rates were significantly higher than those of the control groups of transarterial infusion (TAI) or transarterial chemoembolization (TACE) at the same time (50 0%, 15/30 vs 30 0%, 9/30, P <0 05; 66 7%, 18/27 vs 28 0%, 7/25, P <0 01 and 50 0%, 34 0% vs 33 0%, 3 3%, P <0 01, respectively). Furthermore, the tumor progression rate (10%) in treatment group was significantly lower than that of control group (40 0%, P <0 01). CONCLUSION Double bullet target therapy has a better effect due to the synergistic effects of antibody, radioisotope, and anticancer agents, thus enhancing the tumor killing effect.
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