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NCT06549855Recruiting

PD-1 Inhibitor Combined With Progesterone Treatment in FST for Patients With MMRd Endometrial Cancer

PD-1 Inhibitor Combined With Progesterone Treatment in Fertility Sparing Therapy for Mismatch Repair-deficient Endometrial Cancer

Source: ClinicalTrials.gov · Last updated 10 Aug 2026

Brief summary (registry, in English)

The objective of this study was to investigate the feasibility of a PD-1 inhibitor in combination with progesterone as a means of preserving fertility in patients with early-stage mismatch repair-deficient (MMRd) endometrial cancer who wish to preserve fertility.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
10 (estimated)
First submitted
21 Jul 2024
Start date
2 Sept 2024
Primary completion date
Jul 2029
Lead sponsor
Peking University People's Hospital
NCT number
NCT06549855

What you commit to

  • Study type: Interventional
  • Planned participants: 10
  • From 2 Sept 2024 to the primary completion date, Jul 2029
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Complicated with any other malignancy;

Other

  • Stage IB(FIGO 2009) and above;
  • Tumour differentiation of G3 or non-endometrioid adenocarcinoma;
  • Contraindicated to conservative treatment or the use of pharmaceuticals.
  • Contraindications to pregnancy, or judged by the researcher to be unfit for pregnancy or delivery.

Who the study is looking for

  • Be between the ages of 18-45 years old;
  • Stage IA (FIGO 2009) ;
  • Confirmed diagnosis of endometrial adenocarcinoma G1-G2 based upon D\&C or hysteroscopy;
  • Molecular classification of MMRd, determined by immunohistochemical (IHC) for MMR proteins and by the second generation sequencing (NGS) or microsatellite polymerase chain reaction (PCR);
  • With a strong desire for fertility preservation;
  • Sign the informed consent.

Age in the registry: 18 years to 45 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Peking University People's Hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.