Table 3:
Patient | Regimen | Treatment Time (days) | Discontinuation Reason | Type of Progression | TTF (days) | PFS (days) | Lines before Treatment | Lines after Treatment |
---|---|---|---|---|---|---|---|---|
1 | PD-1/PD-L1 | 153 | POD | radiographic | 167 | 151 | 2 | 1 |
2 | PD-1/PD-L1+CTLA-4 | 14 | POD | clinical/radiographic | 36 | 21 | 7 | 0 |
3 | PD-1/PD-L1+CTLA-4 | 329 | POD | radiographic | 358 | 336 | 4 | 4 |
4 | PD-1/PD-L1+CTLA-4 | 56 | POD | clinical/radiographic | 106 | 81 | 4 | 2 |
5 | PD-1/PD-L1+ targeted therapy | 28 | POD, adverse event (autoimmune neuropathy) | clinical, radiographic | 60 | 43 | 3 | 0 |
6 | PD-1/PD-L1 | 28 | POD | clinical, radiographic | 53 | 49 | 3 | 1 |
7 | PD-1/PD-L1 | 49 | POD | radiographic | 74 | 50 | 2 | 2 |
8 | PD-1/PD-L1+ targeted therapy | 104 | POD | radiographic | 146 | 119 | 3 | 1 |
9 | PD-1/PD-L1+CTLA-4 | 14 | POD | clinical, radiographic | 78 | 45 | 3 | 0 |
10 | PD-1/PD-L1+CTLA-4 | 574 | adverse event (acute liver injury) | N/A | 1568 | 1538 | 1 | 2 |
10 | PD-1/PD-L1+CTLA-4 | 21 | adverse event | N/A | 157a | N/A | 3 | N/A |
11 | PD-1/PD-L1 | 393 | POD | radiographic/biopsy-proven | 402 | 387 | 7 | 2 |
12 | PD-1/PD-L1+CTLA-4 | 383 | N/A | N/A | 383a | N/A | 2 | N/A |
13 | PD-1/PD-L1 | 54 | POD | radiographic | 62 | 55 | 2 | 6 |
14 | PD-1/PD-L1+CTLA-4 | 63 | POD | clinical/radiographic | 99 | 80 | 1 | 0 |
15 | PD-1/PD-L1+ targeted therapy | 15 | POD | clinical/radiographic | 27 | 21 | 2 | 0 |
16 | PD-1/PD-L1+ targeted therapy | 113 | POD | radiographic | 134 | 123 | 2 | 1 |
TTF: time to treatment failure; PFS: progression free survival; PD-1: programmed cell death protein 1; PD-L1: programmed death-ligand 1; CTLA-4: cytotoxic T-lymphocyte–associated antigen 4; POD: progression of disease
these patients continue to have an ongoing response to ICB therapy and remain disease free at the time of database closure. Their duration of response between start of ICB and time of data censoring is indicated here.