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人乳头瘤病毒:一种预防子宫宫颈癌的疫苗

[Human papillomavirus: a vaccine against cervical carcinoma uterine].

作者信息

Franceschi Silvia

机构信息

Field and Intervention Study Unit, International Agency for Research on Cancer, Lyon, France.

出版信息

Epidemiol Prev. 2002 May-Jun;26(3):140-4.

Abstract

Human papillomavirus (HPV) has been identified in fewer than 20 years as the central cause of cervical carcinoma and one of the most powerful known human carcinogens. At least 20 different types of HPV have been associated with relative risks of approximately 100 for both squamous-cell carcinoma and the rarer adenocarcinoma of the cervix uteri. Cytologic screening programs have contributed to the decline of cervical cancer mortality in Europe and the United States. Long-term screening programs remain, however, outside the reach of the poorest countries, where 80% of deaths for cervical carcinoma occurs. More than 20 different types of prophylactic and/or therapeutic vaccines against HPV are being evaluated in clinical or preclinical studies. One such type, a prophylactic vaccine based on the marked immunogenicity and safety of the empty viral capsid, will start being evaluated in 2002 in 3 phase-III randomized studies, mostly in the United States and Latin America. The International Agency for Research on Cancer and World Health Organization are planning, in parallel with the studies above, a double blind randomized phase IV study of approximately 40,000 adolescent and young women in Asia. Such study, which should include a cluster randomization (by village of birth); a comparison with another vaccine (rather than with placebo); and, possibly, the inclusion of adolescents and young adults of male sex. Such trial may accelerate by many years the availability of an anti-HPV vaccine among populations at highest risk for cervical carcinoma.

摘要

人乳头瘤病毒(HPV)在不到20年的时间里被确认为宫颈癌的主要病因,也是已知最强大的人类致癌物之一。至少20种不同类型的HPV与子宫颈鳞状细胞癌和较罕见的子宫颈腺癌的相对风险约为100有关。细胞学筛查计划有助于欧洲和美国宫颈癌死亡率的下降。然而,长期筛查计划仍然是最贫穷国家无法企及的,而这些国家发生了80%的宫颈癌死亡病例。超过20种不同类型的针对HPV的预防性和/或治疗性疫苗正在临床或临床前研究中进行评估。其中一种类型,一种基于空病毒衣壳显著免疫原性和安全性的预防性疫苗,将于2002年开始在3项III期随机研究中进行评估,主要在美国和拉丁美洲。国际癌症研究机构和世界卫生组织正在与上述研究并行,计划在亚洲对约40000名青少年和年轻女性进行一项双盲随机IV期研究。这样的研究应包括整群随机化(按出生村庄);与另一种疫苗进行比较(而不是与安慰剂比较);并且可能纳入男性青少年和年轻人。这样的试验可能会使宫颈癌高危人群中抗HPV疫苗的可及性提前很多年实现。

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