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. 2024 Feb 12;12(2):e008189. doi: 10.1136/jitc-2023-008189

Table 1.

Subsequent systemic therapy for all randomized patients

Nivolumab plus ipilimumab with chemotherapy (n=361) Chemotherapy (n=358)
Received subsequent systemic therapy, n (%) 135 (37) 174 (49)
 Any immunotherapy 26 (7) 130* (36)
  Anti-PD-1 15 (4) 107 (30)
   Nivolumab 11 (3) 72 (20)
   Pembrolizumab 4 (1) 36 (10)
  Anti-PD-L1 8 (2) 24 (7)
  Anti-CTLA-4 2 (1) 2 (1)
   Other immunotherapy 5 (1) 6 (2)
 Targeted therapy 26 (7) 30 (8)
 Chemotherapy 126 (35) 99 (28)
   Platinum-doublet chemotherapy 71 (20) 22 (6)

Percentages based on all randomized patients. Patients may have received more than one type of subsequent therapy. Subsequent therapy was defined as therapy that started on or after the first dosing date (randomization date if the patient was never treated).

*Includes one patient who was randomized to the chemotherapy arm but did not receive treatment.