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โ† Trials
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Molecular and ctDNA Characterization of High-Risk Endometrial Cancer

Recruitingn/aAges 18 Years - anyFemaleMayo Clinic
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In plain words

What the trial is, and whether it could suit you

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.

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: * Age โ‰ฅ 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 \[International Federation of Gynecology and Obstetrics (FIGO) staging used throughout this protocol\] * Preoperatively: * Biopsy with grade 3 endometrioid endometrial cancer (EC) or non-endometrioid EC * Patients with FIGO grade 1-2 EC with evidence of extrauterine disease on imaging (CT, MRI, or PET) * Postoperatively: * Endometrial cancer (FIGO) with one or more established risk factors: * Non-endometrioid histology * Grade 3 * Lymphovascular space invasion (LVSI), โ‰ฅ 50% of myometrial invasion, presence of isolated tumor cells (ITC) in a sentinel lymph node OR * Stage II to IV (FIGO) EC * Provide written informed consent * Willingness to provide mandatory blood specimens for correlative research * Willingness to provide mandatory tissue specimens for correlative research * Willingness to return to registering site for clinical follow-up Exclusion Criteria: * Patient receiving or who has received neoadjuvant chemotherapy * Pre-operative pregnancy
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What it tests

  • Non-Interventional Study
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Where

1 site
Mayo Clinic in Rochester
Rochester, United States
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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