Sun Z, Zhu Y, Stjernsward J, Hilleman M, Collins R, Zhen Y, Hsia C C, Lu J, Huang F, Ni Z
Cancer Institute, Chinese Academy of Medical Science, Beijing, PRC.
Cancer Detect Prev. 1991;15(4):313-8.
A large-scale, controlled study of universal immunization of newborns against HBV infection has been conducted in the high incidence area of hepatocellular carcinoma, Qidong County of China. This area has a stable population, standardized cancer registration system, and an epidemiological base for measurements of liver cancer prevention by vaccine. Randomization was done on the community level. The vaccination and the control group each will consist of 38,000 children by the end of 1990. It is anticipated that the design will provide high statistical power to detect 50% reduction in the prevalence rate of chronic hepatitis among the vaccinees vs. the controls at 6 to 10 years of age, and 50% reduction in the incidence rate of hepatocellular carcinoma at 35 to 40 years of age. The vaccine used is Hep-B Vax, donated by Merck and Co. through WHO. The vaccine was administered at 0, 1, and 6 months after birth, the dosage of 5 or 2.5 micrograms in the pilot study as used before 1985 and of 5 micrograms dose level during the main study starting from January 1, 1985. About 85% of the cohorts have now entered the protocol. The vaccination coverage during 1984 to 1989 was 98.0% (35,064/35,789). Follow-up of the vaccinees and the age-matched controls at 5 years has exceeded 97%. The cumulative mortality in the vaccinated group up to 1988 was 1.29% (354/27,450). No single death nor serious adverse reaction was found that was associated with vaccination. The use of HBV vaccine at a reduced dose was especially important for the developing countries at the present time in order to achieve widespread immunization. Five-year results of the pilot study of this vaccination project showed that significant protection against HBV infection was achieved with the 5 or 2.5 micrograms per dose regimen plus a booster of 5 micrograms given at 3.5 to 4 years of age.(ABSTRACT TRUNCATED AT 250 WORDS)
在中国肝癌高发地区启东县,开展了一项针对新生儿普遍接种乙肝疫苗以预防乙肝感染的大规模对照研究。该地区人口稳定,癌症登记系统规范,具备通过疫苗预防肝癌的流行病学基础。随机分组在社区层面进行。到1990年底,接种组和对照组各将有38000名儿童。预计该设计将具备高统计效力,以检测出接种疫苗儿童与对照组相比,6至10岁时慢性肝炎患病率降低50%,35至40岁时肝细胞癌发病率降低50%。使用的疫苗是默克公司通过世界卫生组织捐赠的乙肝疫苗。疫苗在出生后0、1和6个月接种,1985年前试点研究中剂量为5或2.5微克,自1985年1月1日起主要研究期间剂量为5微克。约85%的队列现已进入研究方案。1984年至1989年期间的疫苗接种覆盖率为98.0%(35064/35789)。对接种疫苗者和年龄匹配对照组的5年随访率超过97%。截至1988年,接种组的累积死亡率为1.29%(354/27450)。未发现与接种相关的单一死亡或严重不良反应。目前,降低剂量使用乙肝疫苗对发展中国家实现广泛免疫尤为重要。该疫苗接种项目试点研究的五年结果表明,每剂5或2.5微克的接种方案加上3.5至4岁时5微克的加强剂量,可有效预防乙肝感染。(摘要截选至250词)
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