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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorMemorial Sloan Kettering Cancer Center

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 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).

Eligibility criteria

Qualifiers

Patients must have pathologically confirmed endometrial cancer

Patients with advanced endometrial cancer

Stage III with residual disease

Stage IV

Disqualifiers

None

Trial design

Treatments tested in this trial

  • ctDNA Testing
  • Blood draw
  • Surveys
  • Semi-structured interviews

Treatment groups

30 Participants
are divided into 2 treatment groups