Study of Antitumor Immune Response After cCRT and IO Treatment in Non-resectable III Stage NSCLC Patients
- Sponsor
- Fundación GECP
- Study ID
- NCT06634199
- Status
- Recruiting
Conditions
- Non-small Cell Lung Cancer Stage III
- PDL1 Gene Mutation
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Durvalumab — DRUGChemo-radiotherapy + Durvalumab for non-resectable stage III NSCLC patients according to clinical practice of each participant hospital
Study Details
Observational, multicenter, one-arm, non-comparative study. Data will be recorded in a retrospectively manner. The study will be based on secondary data collected from patient clinical chart completed by the doctor during routine visits. The primary objective is describe the antitumor immune response generated in the context of IO (immunotherapy) treatment after cCRT in patients with unresectable NSCLC treated in real world.
Key Dates
- Start date
- Oct 3, 2024
- Status verified
- Jan 2026
- Primary completion
- Nov 4, 2027
- Completion
- Nov 4, 2027
Study Design
- Enrollment
- 50 participants (estimated)
Arms
- Arm: Observational Study GroupReal world non-small cell lung cancer (NSCLC) stage IIIA/B and IIIC; PD-L1\>1%; non-resectable patients in treatment with IO after concurrent chemo-radiotherapy without progression.
Primary Outcome Measure
Overall survival (OS) [ Time Frame: To evaluate the Overall Survival at 12, 18, 24 and 36 months ]
Central Contacts
- Eva Pereira+34934302006
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