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

Recruiting

Pragmatic Pilot Study of ctDNA Informed Immune Checkpoint Inhibitor De-escalation in Advanced/Recurrent Mismatch Repair Deficient (MMR-D)/Microsatellite Instability High (MSI-H) Endometrial Cancer Using Standard of Care Treatments

Who can join

Ages 18 and older · Women

Full 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 endometrial cancer after adjuvant therapy only
* Patients can have primary or planned interval surgery
* MMR-D on immunohistochemistry OR MSI-H using any commercially available test
* Patients with treated brain metastases are eligible if follow up brain imaging after CNS directed therapy shows no evidence of progression.
* Eligible for standard of care chemotherapy with immune checkpoint inhibitor per treating investigator with no clinical contraindications
* For the up to 10 patients who are allowed to enroll after C1D1 of standard of care treatments, they need to be on treatment with no clinical evidence of disease progression.

  * Patients may have received prior radiation therapy for treatment of endometrial cancer. Prior radiation therapy may have included pelvic radiation therapy, extended field pelvic/para aortic radiation therapy, intravaginal brachytherapy, and/or palliative radiation therapy.
  * Patients may have received prior hormonal therapy for treatment of endometrial cancer.
  * Patients may not have received prior therapy with an anti-PD-1, anti-PD-L1 or anti-CTLA-4 therapeutic antibody or other similar agents.

    * Except for the up to 10 patients who are allowed to enroll after C1D1 of standard of care treatments (chemotherapy and/or immune checkpoint inhibitors) per protocol.
* Age ≥ 18
* Not Pregnant and Not Nursing

About the study

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 standard chemotherapy and immune checkpoint inhibitor (ICI) treatment to decide whether to continue maintenance ICI treatment past 1 year. The researchers will also look at the health outcomes of people in this study (for example, whether they are cancer free at the end of their participation in the study).

What is being tested

Sponsor: Memorial Sloan Kettering Cancer Center · Participants: 30 · Started: Nov 25, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT07270666

Locations in the U.S.

New JerseyMemorial Sloan Kettering Basking Ridge (All Protocol Activites), Basking Ridge
Memorial Sloan Kettering Monmouth (All Protocol Activities), Middletown
Memorial Sloan Kettering Bergen (All Protocol Activities), Montvale
New YorkMemorial Sloan Kettering Suffolk - Commack (All Protocol Activities), Commack
Memorial Sloan Kettering Westchester (All Protocol Activities), Harrison
Memorial Sloan Kettering Cancer Center, New York
Memorial Sloan Kettering Nassau (All Protocol Activities), Rockville Centre

Conditions

From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.