Cervical caner
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Clinical diagnosis of cervical cancer (IB1-IIA2); 2. Preoperative pathological diagnosis of cervical squamous cell carcinoma, cervical adenosquamous carcinoma or cervical adenocarcinoma 3. Aged <=65 years; 4. Initial treatment; 5. Subjects Volunteer to join the study, sign an informed consent form, have good compliance, and cooperate with follow-up.
Exclusion criteria
Exclusion criteria: 1. Patients' general condition is poor and severe medical complications are difficult to tolerate surgical treatment; 2. Patients who have previously received pelvic/abdominal radiotherapy or chemotherapy; 3. Patients during pregnancy 4. Patients with other gynecological malignancies such as ovarian tumors; 5. CT, MRI or PET suggesting extracervix metastasis; 6. Those who are unable or unwilling to sign the informed consent form, and are unable or unwilling to comply with the research requirements.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 5 year disease free survival; | — |
Countries
China
Contacts
The Obstetrics and Gynecology Hospital of Fudan University