ctDNA Testing to Inform Standard-of-Care Treatment Decisions in People With Endometrial Cancer

Recruiting N/A Interventional Study
Endometrial Cancer
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Female
Study type
Interventional
Purpose
Treatment
Participants needed
30 (estimated)
Sponsor
Memorial Sloan Kettering Cancer Center · Other
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About This Trial
The researchers are doing this study to evaluate the use of circulating tumor DNA (ctDNA) testing in making treatment decisions for advanced/recurrent endometrial cancer that has a change (mutation) in the mismatch repair deficient (MMR-D) gene or microsatellite instability high (MSI-H) gene. The researchers will see how doctors and their patients use the results of ctDNA testing after 1 year of s…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients must have pathologically confirmed endometrial cancer * Patients with advanced endometrial cancer * Stage III with residual disease °Select patients with Stage III disease and no residual disease can be enrolled after discussion with PI * Stage IV * Recurrent endom…
Contacts

Ying Liu, MD, MPH

646-888-4946

liuy6@mskcc.org

CONTACT

Paul Johannet, MD

646-888-5327

CONTACT