The immune-related adverse events (irAEs) linked to the important activation of the immune system by new immunotherapy treatments in patients affected by Non-small-cell lung carcinoma (NSCLC) have not received a lot of systematic study or been monitored over time outside of clinical trials. This study aims to verify, on the basis of the data collected in a prospective and retrospective manner, that the side-effects due of anti-PD-(L)-1 or anti-CTLA-4 treatments observed in the target population of the controlled clinical trials are the same as in the general clinical population.
Study Type
OBSERVATIONAL
Enrollment
80
Gradation of the adverse events according to CTCAE scale 4.03 (June 2010).
Cliniques Universitaires Saint-Luc
Brussels, Belgium
Census and monitor of the side-effects due to the immunotherapy treatment.
Census of the side-effect type, severity according to the CTCAE and monitoring the side-effect's development.
Time frame: Through study completion, an average of 20 months.
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