The purpose of this study is to assess the women's quality of life, who accepted chemotherapy,radiotherapy, concurrent radiochemotherapy or who didn't accept therapy, after operation.
Lead Sponsor
Enrollment
Start Date
Completion Date
Study Type
Official Title
Age Range
Sex
Inclusion Criteria: * ≮ 18 years, cervical cancer verified by pathology, * IIA stage, accepted the operation ( Piver III and pelvic lymph node dissection) as initial therapy, obtained the patient's agreement Exclusion Criteria: * the patient had accepted chemotherapy or radiotherapy before operation