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Using Ex Vivo Tumoroids To Predict Immunotherapy Response In NSCLC — TUMORIN  

Lung Cancer Clinical Trial

Official title:
Using Ex Vivo Tumoroids To Predict Immunotherapy Response In NSCLC (TUMORIN)

Clinical Trial Summary

To test whether it is feasible to perform the 3D-EX functional predictive response bioassay in the context of patients with advanced/metastatic NSCLC receiving immune checkpoint inhibitors in the standard of care clinical setting.

Clinical Trial Description

Non-small cell lung cancer (NSCLC), which accounts for approximately 85% of all lung cancer cases, remains the leading cause of cancer death worldwide. Immunotherapy such as using immune checkpoint inhibitors (ICIs) to target the programmed death-1 and its ligand (PD-1/L1) has revolutionized our management of this deadly disease. However, a large proportion of patients do not derive benefit due to primary, adaptive or acquired resistance. Hence, better identifying this patient population, understanding the resistance mechanism and exploring novel combinations with current SOC immunotherapy are urgently needed to continue to benefit our NSCLC patients. The investigators hypothesize that patient-derived immune cell containing ex-vivo tumoroids could serve these purposes. In this study, the investigators plan to develop such a 3D ex-vivo system utilizing fresh biopsied tissue from NSCLC patients. The investigators plan to prospectively evaluate the value of these ex-vivo tumoroids in immunotherapy naive advanced/metastatic NSCLC patients who will be receiving anti-PD-1/L1 (with or without anti-CTLA-4) per standard-of-care. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05332925
Study type Observational
Source University of Kansas Medical Center
Contact Darlene Kocher
Phone 9135887132
Email dkocher@kumc.edu
Status Recruiting
Phase
Start date July 21, 2022
Completion date February 2027
View Details
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