Endometrial Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People whose cervical cancer has been confirmed by a pathology test to be one of these types: squamous cell carcinoma, adenocarcinoma, or adeno-squamous cell carcinoma
- People diagnosed with stage IIICr cervical cancer, confirmed by a CT, MRI, or PET/CT scan, where at least one affected lymph node measures 15mm or more across its shortest width on imaging
- People with a general health score of 0 or 1 on a standard medical scale (meaning fully active or able to carry out light work), known as an ECOG score
- People whose doctors expect them to live for more than 6 months
- Women of childbearing age whose pregnancy test (blood or urine) is negative within 7 days before enrolling, and who agree to use contraception throughout the trial
- People who have no medical reasons that would make surgery unsafe for them
Who may not be able to join:
- People with an active or uncontrolled serious infection
- People with active hepatitis B, liver cirrhosis, or severely reduced liver function
- People with a history of immune system deficiency, including HIV-positive status or other conditions that weaken the immune system
- People with an active autoimmune disease that currently requires ongoing treatment with immune-suppressing or disease-modifying medications (note: hormone replacement treatments such as thyroid medication, insulin, or low-dose steroids for adrenal or pituitary conditions are not counted as exclusions under this criterion — confirm with trial site)
- People who have previously had lung inflammation (pneumonitis) that required steroid treatment, or who currently have pneumonitis
- People with chronic kidney insufficiency or kidney failure
- People who have been diagnosed with another cancer within the past 5 years and/or who have required treatment for another cancer
- People with a history of heart attack, serious irregular heartbeat, or moderate-to-severe heart failure (classified as NYHA grade 2 or higher)
- People who have received a transplant of donor tissue or a solid organ
- People who have previously had a pelvic artery embolization procedure
- People who have previously had radiation therapy to the pelvic area
- People who have had a partial or full surgical removal of the uterus (hysterectomy)
- People who have previously received immunotherapy or who are currently receiving immunotherapy
- People with a known history of severe allergic reactions to platinum-based chemotherapy drugs, pembrolizumab, or any of their ingredients
- People who need to take medications during the trial that can cause serious liver or kidney damage — for example, certain treatments for tuberculosis (confirm with trial site)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Dongling Zou, M.D., Chongqing University Cancer Hospital
Phone: 13657690699
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
PFS
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.