Multidimensional Omics Analysis in Malignant Pleural Mesothelioma
Condition(s) studied
Study summary
Malignant pleural mesothelioma (MPM) is a rare and incurable cancer. Most patients are diagnosed with unresectable disease for which treatment options are limited. The lack of prognostic biomarkers further complicates the decision-making. Recently, the introduction of immune checkpoint inhibitors (ICIs) has marked a shift but has failed to produce significant benefits for a large proportion of patients. Maximizing the efficiency of ICIs and developing new protocols to improve drug efficacy is the best possible strategy for improving the life expectancy and quality of life of patients with MPM. This study aims to characterize the organization of the immune system infiltrating mesothelioma and the dynamics of its interaction with the tumor. The rationale is that deciphering this complexity will help improve our understanding of the mechanisms underlying this disease and provide a new tool to optimize the use of ICIs in these patients.
Eligibility
Primary outcome measure(s)
- High-resolution mapping of the organization of the tumor-infiltrating immune system in MPM — 36 months
Characterization of the composition, functional state, and spatial organization of tumor-infiltrating immune cells using integrated bulk, single-cell, and spatial transcriptomic analyses on tumor tissues and malignant pleural effusions.
Trial sites (4)
| Facility | City | Region | Status |
|---|---|---|---|
| Azienda Ospedaliera Universitaria Policlinico Rodolico San Marco di Catania | Catania | Italy | Recruiting |
| Azienda Ospedaliera Universitaria Luigi Vanvitelli, Napoli | Naples | Italy | Recruiting |
| Azienda USL IRCCS di Reggio Emilia | Reggio Emilia | Italy | Recruiting |
| Fondazione Policlinico Universitario Agostino Gemelli IRCCS | Roma | Italy | Recruiting |
More Azienda USL Reggio Emilia - IRCCS trials in Italy
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07561190 on ClinicalTrials.gov ↗ ← All trials in Italy