Bar Plot from Scientific Research

Rates of adverse events of special interest (AESIs) in the neoadjuvant period in Arm 4. Data are shown for the safety population, which consisted of all patients who received at least one dose of any study intervention. Only the neoadjuvant period is shown owing to the maturity of the data. Patients with multiple occurrences in the same category were counted once per category regardless of the number of occurrences.

DOI