Table 2. . Phase III trial efficacy and safety results of pembrolizumab, nivolumab and ipilimumab.
Drug(s) | Response rate (RECIST) | Median PFS (months) | Median OS (months) | Toxicity | Ref. |
---|---|---|---|---|---|
Pembrolizumab (ipilimumab-naive) | 33%† | 4.8† | Not reached; 12-month OS 71% | Fatigue, diarrhea, rash, pruritus | [16] |
Nivolumab (ipilimumab-treated) | 32% | 4.7 | Not reported | Fatigue, pruritus, diarrhea, nausea | [21] |
Nivolumab (first-line) | 40% | 5.1 | Not reached; 12-month OS 73% | Fatigue, pruritus, nausea, diarrhea | [20] |
Ipilimumab + dacarbazine | 15% | 3.0 | 11.2 | Pyrexia, diarrhea, increased hepatic transaminases, pruritus | [24] |
Ipilimumab + Gp100 vaccine | 11% | 2.8 | 10 | Diarrhea, nausea, fatigue, skin toxicity | [23] |
Ipilimumab + nivolumab | 58% | 11.5 | Not reported | Diarrhea, fatigue, pruritus, rash | [15] |
†Mean value of the two dose cohorts of pembrolizumab (2 mg/kg 2 and 3 weekly).
OS: Overall survival; PFS: Progression-free survival; RECIST: Response evaluation criteria in solid tumors.