TABLE 1.
Arm A N = 6 |
Arm B N = 6 |
Arm C N = 6 |
Arm D N = 6 |
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Regimen |
Cisplatin Gemcitabine Nivolumab |
Cisplatin Pemetrexed Nivolumab |
Carboplatin Paclitaxel Bevacizumab Nivolumab |
Docetaxel Nivolumab |
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Adverse event | Any grade | Grade 3‐4 | Any grade | Grade 3‐4 | Any grade | Grade 3‐4 | Any grade | Grade 3‐4 |
Hematologic toxicities | ||||||||
White blood cell count decreased | 6 (100) | 0 (0.0) | 5 (83.3) | 0 (0.0) | 6 (100) | 3 (50.0) | 6 (100) | 5 (83.3) |
Neutrophil count decreased | 6 (100) | 1 (16.7) | 5 (83.3) | 1 (16.7) | 6 (100) | 6 (100) | 6 (100) | 6 (100) |
Lymphocyte count decreased | 4 (66.7) | 0 (0.0) | 1 (16.7) | 0 (0.0) | 4 (66.7) | 1 (16.7) | 5 (83.3) | 3 (50.0) |
Anemia | 6 (100) | 0 (0.0) | 4 (66.7) | 0 (0.0) | 4 (66.7) | 1 (16.7) | 4 (66.7) | 0 (0.0) |
Platelet count decreased | 6 (100) | 0 (0.0) | 3 (50.0) | 0 (0.0) | 6 (100) | 2 (33.3) | 0 (0.0) | 0 (0.0) |
Antiangiogenic adverse events | ||||||||
Hypertension | 1 (16.7) | 0 (0.0) | 1 (16.7) | 1 (16.7) | 4 (66.7) | 0 (0.0) | 0 (0.0) | 0 (0.0) |
Proteinuria | 0 (0.0) | 0 (0.0) | 0 (0.0) | 0 (0.0) | 2 (33.3) | 0 (0.0) | 1 (16.7) | 0 (0.0) |
Epistaxis | 0 (0.0) | 0 (0.0) | 0 (0.0) | 0 (0.0) | 4 (66.7) | 0 (0.0) | 0 (0.0) | 0 (0.0) |
Data are presented as n (%), with n referring to the number of events.