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From Fetal-maternal Interface Immune Tolerance to Endometrial Cancer Immune Escape: Potential Targets for Immunotherapy

From Fetal-maternal Interface Immune Tolerance to Endometrial Cancer Immune Escape: Potential Targets for Immunotherapy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06273878
Enrollment
80
Registered
2024-02-23
Start date
2023-01-15
Completion date
2025-01-15
Last updated
2024-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometrial Cancer

Brief summary

Non-interventional retro-prospective study on Endometrial tissue samples taken from surgically treated patients.

Detailed description

The picture of precisely coordinated immune adaptations over time at the maternal-fetal interface level and altered in pregnancy complications, could reveal a specific immune clock in tumors. The study aims to decipher mechanisms of immunodeficiency by helping to predict recurrence in patients with endometrial cancer and identify molecular pathways that are turned on or off in progression from lesions early to advanced neoplasia. This will allow the discovery of potential immunotherapy targets to interfere with the immune escape activation process or to reactivate/re-educate the immune response.

Interventions

None listed

Sponsors

Università degli Studi dell'Insubria
CollaboratorOTHER
Regina Elena Cancer Institute
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \>18 years; * Histological diagnosis of endometrial hyperplasia with and without atypia, carcinoma of the endometrium histotype endometrioid at any stage of the disease (FIGO I-IV), patients subjected to hysterectomy for benign extra-endometrial pathology, patients with recurrence/metastasis from endometrioid endometrial carcinoma that are subjected to surgery; * Adequate biological material to be able to carry out the analyzes previously described; * Written informed consent (only for patients in the prospective part and/or in follow-up); * For the retrospective part: availability of samples adequately stored at the Institute biobank and availability of follow-up data.

Exclusion criteria

* Comorbidities not controlled with adequate medical therapy; * Infections of the endometrial cavity (pyometra); * Synchronous tumors; * Neoadjuvant treatments; * Previous radiation treatments on the pelvic region.

Design outcomes

Primary

MeasureTime frameDescription
Validate the differential expression of LOX-1 and NALP3 receptors.36 monthsValidate the differential expression of LOX-1 and NALP3 receptors at different steps progression of endometrial cancer; identify immune signatures shared between using transcriptomics the maternal-fetal interface and the different stages of progression of endometrial cancer; investigate their role functional in the immune escape process in endometrial carcinoma and/or in the pro-inflammatory response.

Secondary

MeasureTime frameDescription
Characterize phenotypic alterations.36 monthsCharacterize the phenotype and functional alterations of multiple candidate biomarkers relevant selected in AIM1 (surface antigens / cytokines / molecular pathways), a level of the cells of the immune infiltrate, in the different stages of cancer progression to the endometrium.
Evaluate the predictive and/or prognostic value.36 monthsEvaluate the predictive and/or prognostic value of the immuno-score deriving from the data of Aim 1 and Aim 2 alone or in combination with clinical and prognostic risk factors known histopathological findings, expressed in the ESMO-ESGO-ESTRO consensus conference.

Countries

Italy

Contacts

Primary ContactBenito Chiofalo, Doctor
benito.chiofalo@ifo.gov.itND
Backup ContactValentina Bruno, Doctor
valentina.bruno@ifo.gov.itND

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026