Cancer of Cervix Clinical Trial
Cervical cancer is the most frequent neoplasm of women in Taiwan and in the world. It
influences about 2,700 women with about 1,000 women dying of cervical cancer each year and
in Taiwan. Human papillomaviruses (HPV) have been consistently implicated in causing
cervical cancer especially those high-risk types which have been strongly associated with
cervical cancer. In recent years, there has been compelling evidence that infection with
human papillomavirus (HPV) is a major etiologic factor in the development of cervical
intraepithelial neoplasia (CIN) and cervical carcinoma.
As in most virus-induced diseases, an adequate immune response is likely to play a key role
in the clearance of HPV infections and HPV-related lesions. This assumption is born out by
both epidemiological studies and animal models. Immune-compromised patients such as
HIV-infected women, organ transplant recipients, and patients suffering from other forms of
malignancies, are at a higher risk of developing CIN lesions and invasive cervical cancer.
Moreover, several studies establish the existence of natural HPV E7-specific cytotoxic T
lymphocyte (CTL) immunity in humans. Only a minority of women infected with oncogenic HPV
types develop CIN or cervical cancer. Indeed, the majority of CIN lesions do not progress or
even regress to normal cytology, indicating that other factors such as an inadequate immune
function are necessary for the development of progressive CIN lesions and cervical
carcinoma.
Consequently, the HLA class I and II phenotypes may be correlated with an effective immune
response against HPV-associated cervical lesions. Differences in the recognition of foreign
antigens, such as those contributed by alleles at the HLA class I or II loci, might be
proposed to affect the risk of developing cervical cancer.
In the present proposal, the investigators would like to examine the HLA class I and II
associations among Taiwanese women with cervical neoplasia. The purposes of this proposal
are:
1. to address the relationships between the HLA class I and II haplotype, HPV infection,
and cervical cancer; and
2. to elucidate the immunologic responses to HPV type 16 in different HLA class I and II
haplotypes. It will help the investigators to identify which population of HLA
genotypes is more susceptible to HPV infection and progresses to invasive cervical
cancer. The results of this research will be very useful for the prevention and
screening of cervical cancer in the future.
1. To survey the incidence of HPV infection in CIN and cervical cancer patients.
Using epidemiologic data drawn from a wide range of countries and population groups,
investigators have found evidence of HPV in 90% to 95% of cervical cancers. The
incidence of HPV in cervical cancer was 79% in our own report. Besides, 91% of
high-grade CIN cases and 50% of low-grade CIN cases could be attributed to HPV
infection in Taiwanese women. Because these reports for Taiwanese women were published
around 10 years ago, it is important to survey and update the incidence of HPV in CIN
and cervical cancer patients in Taiwanese women. We will survey the incidence of HPV
infection in 500 cervical cancer patients, 100 patients of CIN and 100 normal
population patients.
2. To survey the human leukocyte antigen haplotype in CIN and cervical cancer patients.
HLA class I and II alleles have been reported to associate with the nasopharyngeal
carcinoma in Taiwan. Besides, human leukocyte antigen class I and II alleles might
interplay in the response to interferon-alpha treatment in Taiwanese patients with
chronic hepatitis C virus infection. We will detect the HLA class I and II haplotype
first and then correlate them with the CIN and cervical cancer patients.
3. To identify the correlation between HLA class I and II haplotype and HPV infection and
CIN and cervical cancer.
We will further survey the correlation between HLA class I and II and the genotypes of
HPV in CIN and cervical cancer patients. We will identify which HLA class I and II
haplotypes have positive or negative correlation with HPV infection, CIN and cervical
cancer. Then we would determine which specific HLA antigens are important in
determining the risk of HPV infection, CIN and cervical cancer.
4. To elucidate the immunologic responses to HPV type 16 in HLA2 with different II
haplotypes and the role of immunogenetics in the carcinogenesis of cervical cancer.
HPV type 16 has been identified to be the highest incidence of malignant HPV genotypes in
cervical cancer. Our laboratory has set up immunologic assays for evaluating the immune
responses to HPV type 16. We will survey the immune response to HPV type 16 in those HLA
class I and II haplotypes which have positive or negative correlation with the HPV infection
and cervical cancer. We would identify which population of HLA genotype are more susceptible
to HPV infection and invasive cervical cancer and elucidate the role of immunogenetics in
the HPV infection and carcinogenesis of cervical cancer.
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Observational Model: Defined Population, Primary Purpose: Screening, Time Perspective: Longitudinal
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