Cervical cancer
Conditions
Interventions
Experimental group (Radical surgery + para-aortic lymph node dissection):none
Control group (Radical surgery):none
Sponsors
Obstetrics & Gynecology Hospital of Fudan University
Eligibility
Sex/Gender
Female
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: Clinical diagnosis of cervical cancer (FIGO stage 2018: stage IB2-IIA2); Preoperative pathological diagnosis is cervical squamous cell carcinoma, cervical adenocarcinoma or cervical adenocarcinoma; Age =60 points; Primarily treated; Participants who voluntarily join the study, sign informed consent with good compliance.
Exclusion criteria
Exclusion criteria: Patients with poor general condition and severe medical complications that are difficult to tolerate surgical treatment; Patients who have previously received pelvic/abdominal radiation or chemotherapy; Pregnant patients; Patients with other gynecological malignancies such as ovarian tumors; CT, MRI or PET suggest extrinsic cervical metastasis; Unable or unwilling to sign informed consent, unable or unwilling to comply with research requirements.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| overall survival;Progression-free survival; | — |
Secondary
| Measure | Time frame |
|---|---|
| quality of life; | — |
Countries
China
Contacts
Public ContactJunjun Qiu
Obstetrics & Gynecology Hospital of Fudan University
Outcome results
None listed