Cervical cancer
Conditions
Interventions
Treatment group:Postoperative standard adjuvant treatment + increase and exemption of tumor suppression prescription granules
Control group:Postoperative standard adjuvant therapy + placebo granules
Sponsors
Obstetrics & Gynecology Hospital of Fudan University
Eligibility
Sex/Gender
Female
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: (1) Patients with a clear pathological diagnosis of cervical cancer, surgical pathological stage IB3, IIA2, IIIC (FIGO stage in 2018), and high-risk factors requiring postoperative complementary treatment. (2) Age 18-70 years old. (3) Normal cardiopulmonary function, liver and kidney function. (4) Subjects who are informed and voluntarily sign the informed consent form. (5) Karnofsky (KPS) score = 70 points.
Exclusion criteria
Exclusion criteria: (1) Severe liver and kidney function impairment. (2) Pregnancy or lactation. (3) Malignant tumors in other parts (= 5 years). (4) Allergy and intolerance to chemotherapy and other drugs. (5) Patients with severe psychological or mental illness. (6) Those who have poor compliance with treatment or follow-up. (7) Karnofsky (KPS) score < 70 points.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Progression-Free Survival; | — |
Secondary
| Measure | Time frame |
|---|---|
| Overalsurvival;Quality of Life scale score;The occurrence of adverse reactions in radiotherapy, chemotherapy and immunotherapy;mental state; | — |
Countries
China
Contacts
Public ContactJianghua
Obstetrics & Gynecology Hospital of Fudan University
Outcome results
None listed