Molecular and ctDNA Characterization of High-Risk Endometrial Cancer

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorMayo Clinic

About this trial

This study seeks to better understand the recurrence of high-risk endometrial cancer. It will collect information about cancer genetics to find out various hereditary or cancer specific genetic variants that may have a role in diagnosis or management and prognosis of cancer. It also seeks to develop a genetic results and medical record databank for future studies.

Eligibility criteria

Qualifiers

Age ≥ 18 years

Planned complete surgical staging at Mayo Clinic. Complete surgical staging includes at least total hysterectomy, bilateral salpingo-oophorectomy and lymph node assessment. Sentinel node mapping meets the criteria for lymph node assessment. Peritoneal cytology is recommended. Additional staging procedures such as pelvic and para-aortic nodal evaluation, omental biopsy or omentectomy, may also be utilized for staging in patients based on the clinical situation and at the surgeon's discretion

At least one preoperative or postoperative feature of aggressive disease [International Federation of Gynecology and Obstetrics (FIGO) staging used throughout this protocol]

Biopsy with grade 3 endometrioid endometrial cancer (EC) or non-endometrioid EC

Disqualifiers

Patient receiving or who has received neoadjuvant chemotherapy

Pre-operative pregnancy

Trial design

Treatments tested in this trial

  • Non-Interventional Study

Treatment groups

100 Participants
are divided into 1 treatment group

Sponsors and collaborators