Cervical cancer
Conditions
Interventions
normal cervical tissue vs. cervical cancer tissue:Nil
Sponsors
Peking Union College of Gynecology and Obstetrics, Tongji Medical College, Huazhong University of Science and Technology
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Patients with cervical cancer met the inclusion criteria. 1. There were no radiotherapy, chemotherapy and biological targeted therapy before cervical tissue sampling, and all cases were confirmed by pathology; 2. The subjects are not restricted by nationality, race and age; 3. Patients who agree to participate in the trial and sign informed consent, and can be followed up regularly; 4. Patients can provide blood and tumor tissue samples; 5. ECoG score was 0 or 1; 6. Good organ function.
Exclusion criteria
Exclusion criteria: 1. Patients with the following serious complications: heart disease, liver disease, kidney disease, endocrine disease, etc.; 2. Patients with infectious diseases; 2. Patients with undiagnosed abnormal genital tract bleeding; 3. Patients with other tumors; 4. Doctors judge the unsuitable subjects; 5. Patients with history of alcoholism and drug abuse (within 6 months before the trial); 6. The subjects used other experimental drugs within 1 month before the test.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| cervical tissue; | — |
Countries
China
Contacts
Public ContactWang Hongbo
Peking Union College of Gynecology and Obstetrics, Tongji Medical College, Huazhong University of Science and Technology
Outcome results
None listed