uterine sarcoma
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. pathological confirmed of uterine sarcoma; 2.FIGO I-II stage; 3. Patients with expected survival >=6 months; 4. Patients aged 18 to 80 years; 5. Patients with ECOG 0-1; 6. Patients with sufficient main organ function (1) Hemopoietic function: hemoglobin >= 100g/L, platelet >= 90 x 10^9/L, neutrophil >= 1.5 x 10^9/L; (2) Renal function: serum creatinine SCR < 1.5 ULN; (3) Liver function: ALT and AST < ULN one point five Times, bilirubin <1.5 x ULN; 7. The patient must sign the informed consent of receiving concurrent radiotherapy and chemotherapy.
Exclusion criteria
Exclusion criteria: 1. Patients who have previously suffered from or complicated with other malignant tumors (except melanoma skin tumors) and whose diseases are not controlled or cured (depending on the disease type of the primary tumor); 2. Patients with congenital or acquired immune deficiency; 3. HIV positive patients, including those who have received antiretroviral therapy; chronic hepatitis B, virus replication period; active period of hepatitis C; 4. Pregnancy (confirmed by serum or urine beta- hCG test) or lactation period; 5. The general condition of the patients was poor, KPS < 70; 6. Patients have conditions that researchers believe may increase the risk of treatment or have serious uncontrollable complications.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| overall survival;Pathological remission rate;progression-free survival; | — |
Secondary
| Measure | Time frame |
|---|---|
| adverse events; | — |
Countries
China
Contacts
International Peace Maternal and Child Health Center affiliated to Shanghai Jiaotong University