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. 2023 May 15;29(6):1370–1378. doi: 10.1038/s41591-023-02347-y

Table 2.

Summary of AEs related to treatment

Grade 1 Grade 2 Grade 3 Grade 4 Grade 5 Total
n (%) n (%) n (%) n (%) n (%) n (%)
AE related to treatment
 Overall frequency 6 (12%) 16 (33%) 11 (22%) 1 (2%) 0 (0%) 34 (69%)
 Brain edema 2 (4%) 8 (16%) 7 (14%) 1 (2%) 0 (0%) 18 (37%)
 Headache 4 (8%) 9 (18%) 2 (4%) 0 (0%) 0 (0%) 15 (31%)
 Fatigue 7 (14%) 7 (14%) 0 (0%) 0 (0%) 0 (0%) 14 (29%)
 Dysphasia 4 (8%) 4 (8%) 0 (0%) 0 (0%) 0 (0%) 8 (16%)
 Hemiparesis 0 (0%) 2 (4%) 4 (8%) 0 (0%) 0 (0%) 6 (12%)
 Pyrexia 5 (10%) 0 (0%) 0 (0%) 0 (0%) 0 (0%) 5 (10%)
 Decreased appetite 3 (6%) 1 (2%) 0 (0%) 0 (0%) 0 (0%) 4 (8%)
 Myalgia 2 (4%) 2(4%) 0 (0%) 0 (0%) 0 (0%) 4 (8%)
 Nausea 2 (4%) 2(4%) 0 (0%) 0 (0%) 0 (0%) 4 (8%)
SAE related to treatment
 Overall frequency 0 (0%) 4 (8%) 9 (18%) 1 (2%) 0 (0%) 14 (29%)
 Brain/vasogenic edema 0 (0%) 1 (2%) 6 (12%) 1 (2%) 0 (0%) 8 (16%)
 Dysphasia 0 (0%) 3 (6%) 0 (0%) 0 (0%) 0 (0%) 3 (6%)
 Hemiparesis 0 (0%) 0 (0%) 3 (6%) 0 (0%) 0 (0%) 3 (6%)

AE denotes adverse event. SAE denotes serious adverse event. Shown are AEs and SAEs with greater than 5% frequency. Overall frequency refers to patients reporting at least one treatment related AE. Each patient is included once using the highest-grade event. Events were graded according to National Cancer Institute-Common Terminology Criteria for Adverse Events, version 4.03.