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Recruiting NCT07690540

DETERMINANTS OF IMMUNOTHERAPY EFFICACY IN ENDOMETRIAL CANCER

No phase Interventional Endometrial Cancer Immune Checkpoint Inhibitors

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Prospective exploratory cohort.
Who it may be relevant to
Registry conditions: Endometrial Cancer, Immune Checkpoint Inhibitors. Basic parameters: from 18 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

INVESTIGATING DETERMINANTS OF IMMUNOTHERAPY EFFICACY IN ENDOMETRIAL CANCER: A MULTIDIMENSIONAL APPROACH IN A UNIQUE POPULATION (iDEA PROJECT)

Overview

In recent years, the introduction of immune checkpoint inhibitors (ICI) in combination with chemotherapy has significantly changed the management of advanced and recurrent Endometrial Cancer (EC). Despite these advances, responses to immunotherapy remain heterogeneous. Not all patients with mismatch repair-deficient (dMMR) tumors derive durable benefit, while a subset of mismatch repair-proficient (pMMR) tumors may respond. In addition, ICI treatment is associated with relevant costs and immune-related toxicities, highlighting the need for improved patient selection. To date, no validated predictive biomarkers beyond mismatch repair (MMR) status are available, reflecting limited understanding of the biological mechanisms underlying sensitivity and resistance to immunotherapy in EC. This study aims to assess and integrate molecular and epigenetic features to identify prognostic and predictive biomarkers of immunotherapy response in endometrial cancer, and to explore their functional relevance using patient-derived experimental models.

Interventions

  • Biological Prospective exploratory cohort
    Fresh tumor samples, paired with FFPE tissue, will be collected prior to initiation of immunotherapy and will be used to generate patient-derived three-dimensional tumoroids on a microfluidic organ-on-chip platform.

Primary outcome measures

  • Progression-Free Survival [Time frame: 2 years]
  • Overall Survival [Time frame: 2 years]

Eligibility criteria

Inclusion criteria

  • Age ≥ 18 years
  • Histologically confirmed advanced or recurrent endometrial carcinoma or carcinosarcoma
  • No prior treatment with immune checkpoint inhibitors
  • Availability of paired fresh-frozen and FFPE tumor samples
  • Provision of written informed consent for participation in translational research

Exclusion criteria

  • Refusal or inability to provide informed consent by the patient or legal representative
  • Mesenchymal tumors or epithelial tumors of non-endometrial origin (e.g., ovarian cancer)
  • Active treatment with immunomodulatory agents at the time of sample collection (e.g., immunotherapy for autoimmune disease)
  • Known positivity for HIV, hepatitis B virus (HBV), or hepatitis C virus (HCV)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Other

Study locations

Italy · 1 center
  • European Institute of Oncology — Milan

Identifiers

NCT: NCT07690540 · UID 5328 · L2-593

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗