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An experimental vaccine has been found to be 100% effective at preventing the most common forms of cervical cancer, according to results of a two-year study. announced by Merck and Co. at the annual meeting of the Infectious Diseases Society of America. The study, which involved more than 12,000 women from 13 countries, showed that the genetically engineered vaccine called Gardasil blocked infection of two common strands of the human papillomavirus (HPV), a common sexually transmitted disease. Merck expects to receive approval by the U.S. Food and Drug Administration (FDA) by the end of the year and begin offering the vaccine to pre-sexually active girls in 2006. "To have 100 percent efficacy is something that you have very rarely," Dr. Eliav Barr, Merck's head of clinical development for Gardasil, told The Associated Press. The study results were announced in October 2005 by Merck and Co. at the annual meeting of the Infectious Diseases Society of America. The vaccine works by preventing infection from two forms of HPV, a common sexually transmitted disease that affects both men and women. There are over 80 different strains of HPV and most do not pose any health risks. However, some strains of HPV (in particular, HPV-16, HPV-18, HPV-31, and HPV-45) can cause cellular changes that may lead to cervical cancer in women. The vaccine blocks HPV-16 and HPV-18, which account for about 70% of cervical cancer cases. An estimated 20 million American men and women are carrying HPV. According to the American Cancer Society, approximately 13,000 women will develop invasive cervical cancer this year, and about 4,100 women will die of the disease. Cervical cancer is more prevalent in less developed countries were accessed to screening is limited. Many experts see the study results as a major break-through, though they acknowledge that published results are needed. In a formal statement, Debbie Saslow, Ph.D., director of breast and gynecological cancers for the American Cancer Society, called the vaccine an exciting advancement but noted that the data must be peer-reviewed and published. If the vaccine is FDA-approved, it will likely need to be offered to both young women and young men. While men cannot get cervical cancer because they do not have cervixes, they can carry HPV and infect women through sexual intercourse. Moreover, experts say that because there is no evidence that the vaccine will work on women that already have an HPV infection, guidelines for cervical cancer screening will still need to be followed even if the vaccine receives FDA approval. The American Cancer Society guidelines are as follows:
Source: American Cancer Society
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