About this trial
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.
Eligibility criteria
Qualifiers
Patients with histologically- or cytologically- documented NSCLC who present unresectable stage IIIA-IIIB-IIIC disease, according to 8th version of the International Association for the Study of Lung Cancer Staging Manual in Thoracic Oncology).
ECOG 0-1.
PDL1>1%.
Age ≥ 18 years at time of study
Disqualifiers
Patients who refuse to sign and date an IRB/IEC-approved written informed consent form.
No possibility of venipuncture
Any medical, mental, or psychological condition which in the opinion of the investigator would not permit the patient to complete the study or understand the patient information.
Trial design
Treatments tested in this trial
- Durvalumab