Morris Shaun K, Nguyen Claire K
Division of Infectious Diseases, The Hospital for Sick Children and The University of Toronto, Toronto, ON.
Can J Public Health. 2008 Mar-Apr;99(2):114-6. doi: 10.1007/BF03405456.
Clinical studies have shown the human papillomavirus (HPV) vaccines to be very effective at preventing persistent infection by vaccine serotypes. The development of these new vaccines heralds a new era in cancer prevention. Gardasil, Merck's quadravalent HPV vaccine, has recently been licensed in Canada for women aged 9 to 26 years of age. It necessitates that health professionals become familiar with the vaccine, the evidence supporting its effectiveness and issues related to vaccine strategy, cost effectiveness, and remaining research questions. The vaccine is recommended in Canada for females aged 9 to 13 years and should also be offered to females aged 14 to 26 years. Ongoing research will determine the duration of protection conferred by the vaccine, and the potential need for booster doses. In conjunction with continued screening programs, the HPV vaccine offers the potential to dramatically reduce the burden of cervical cancer in Canada, and to do so in a cost-effective manner.
临床研究表明,人乳头瘤病毒(HPV)疫苗在预防疫苗血清型的持续感染方面非常有效。这些新疫苗的研发预示着癌症预防的新时代。默克公司的四价HPV疫苗加德西(Gardasil)最近在加拿大获得许可,适用于9至26岁的女性。这就要求卫生专业人员熟悉该疫苗、支持其有效性的证据以及与疫苗策略、成本效益和剩余研究问题相关的事项。在加拿大,该疫苗推荐给9至13岁的女性,也应提供给14至26岁的女性。正在进行的研究将确定该疫苗提供的保护持续时间以及是否可能需要加强剂量。与持续的筛查计划相结合,HPV疫苗有可能大幅减轻加拿大宫颈癌的负担,并且以具有成本效益的方式做到这一点。