| Pap Smear | ![]() |
| Cervical cancer
is one of the most common cancers, accounting for 6% of
all malignancies in women. There are an estimated 16,000
new cases of invasive cancer of the cervix and 5,000
deaths in the U.S. each year. The prognosis for this disease is markedly affected by the extent of disease at the time of diagnosis. Because a vast majority (greater than 90%) of these cases can and should be detected early through the use of the Pap smear, the current death rate is far higher than it should be and reflects that, even today, Pap smears are not done on approximately one-third of eligible women. Among the major factors that influence prognosis are stage, volume and grade of tumor, histologic type, lymphatic spread, and vascular invasion. Human immunodeficiency virus-infected women have more aggressive and advanced disease and a poorer prognosis. New Test for Cervical Cancer |
Human papillomavirus
infection and cervical cancer Molecular techniques for the identification of human papillomavirus (HPV) DNA are highly sensitive and specific. It is estimated that more than 6 million women in the United States have HPV infection. Epidemiologic
studies convincingly demonstrate that the major risk
factor for development of preinvasive or invasive
carcinoma of the cervix is HPV infection,
which far outweighs other known risk factors such as Some patients with HPV infection appear to be at minimal increased risk for development of cervical preinvasive and invasive malignancies while others appear to be at significant risk and candidates for intensive screening programs and/or early intervention. However, use of a positive HPV DNA test to indictate more in-depth evaluation of the patient may lead to unwarranted and ineffective treatment and/or unnecessary patient anxiety. Conversely, current technology may be too insensitive to detect small amounts of potentially tumorigenic HPV types leading to a false sense of security. Clearly the patient with an abnormal cervical cytology of a high-risk type (Bethesda Classification) should be thoroughly evaluated with colposcopy and biopsy. Patients with low-risk cytology (Bethesda Classification) may or may not have preinvasive or microinvasive cancer and HPV DNA typing may aid in differentiating which patients to evaluate intensively and which to follow more conservatively. Other studies show patients with low-risk cytology and high-risk HPV infection with types 16, 18, and 31 are more likely to have cervical intraepithelial neoplasia (CIN) or microinvasive histopathology on biopsy. Studies suggest that acute infection with HPV types 16 and 18 conferred an 11- to 16.9-fold risk of rapid development of high-grade CIN. HPV typing may prove useful, particularly in patients with low-grade cytology or cytology of unclear abnormality. |