Table 2.

Incidence and management of CRS and neurotoxicity

Group 1 (n = 11)Group 2 (n = 18)P
CRS    
Any grade, n (%) 5 (45) 7 (39) 
Grade ≥3, n (%) 1 (9)  1 (6)  
Median time to onset, d (range) 4 (1-6) 6 (3-10) .05 
Median duration, d (range) 8 (5-19) 3 (1-20) .08 
Neurotoxicity    
Any grade, n (%) 3 (27) 2 (11) .34 
Grade ≥3, n (%) 1 (9)  1 (6)  
Treatment for CRS and neurotoxicity    
Tocilizumab, n (%) 1 (9) 1 (6) 
Steroids, n (%) 1 (9) 2 (11) 
Tocilizumab and steroids, n (%) 1 (9) 1 (6) 
Group 1 (n = 11)Group 2 (n = 18)P
CRS    
Any grade, n (%) 5 (45) 7 (39) 
Grade ≥3, n (%) 1 (9)  1 (6)  
Median time to onset, d (range) 4 (1-6) 6 (3-10) .05 
Median duration, d (range) 8 (5-19) 3 (1-20) .08 
Neurotoxicity    
Any grade, n (%) 3 (27) 2 (11) .34 
Grade ≥3, n (%) 1 (9)  1 (6)  
Treatment for CRS and neurotoxicity    
Tocilizumab, n (%) 1 (9) 1 (6) 
Steroids, n (%) 1 (9) 2 (11) 
Tocilizumab and steroids, n (%) 1 (9) 1 (6) 

CRS was graded according to the Lee criteria. Neurotoxicity was graded using the CTCAE v4.03. P values per Wilcoxon rank-sum test or Fisher exact test (2-sided), as appropriate.

Patient with grade 5 CRS and neurotoxicity who did not receive any durvalumab dose.

Patient from durvalumab 225 mg dose level with grade 4 CRS (DLT).

Patient from durvalumab 750 mg dose level with prolonged grade 3 neurotoxicity (DLT).

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