C54 C53 C56 D07
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients who underwent fertility-sparing surgery for endometrial cancer (C54.-), cervical cancer (C53.-), and ovarian cancer (C56.-) Patients with borderline ovarian tumors (C56.-) Patients with atypical endometrial hyperplasia (D07.0; N85.0; N85.1; N85.9)
Exclusion criteria
Exclusion criteria: Patients younger than 18 years and patients in whom a primary fertility-sparing approach was not performed are excluded from the study cohort. As the questionnaires are administered in German, patients who are unable to read or complete them are also excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary study endpoints are overall survival (OS), recurrence-free survival (RFS), pregnancy rates, and live birth rates. These will be assessed through patient interviews and questionnaires. | — |
Secondary
| Measure | Time frame |
|---|---|
| Assessment of oncologic and reproductive outcomes following fertility-sparing treatment in gynecologic malignancies and precancerous lesions, including time to pregnancy, pregnancy outcomes, timing of diagnosis in relation to pregnancy, rates of completion surgery after childbearing, and effects on quality of life and sexual function. | — |
Countries
Germany
Contacts
Universitätsklinikum Erlangen - Frauenklinik