Table 2.
Agent | Trading name | Antibody | Dose and schedule | Phase | Trial name | Patients number | Main results | Reference |
---|---|---|---|---|---|---|---|---|
Pembrolizumab | Keytruda | PD-1 | 200 mg, every 3 weeks | 3 | Keynote-045 | 542 (270 versus 272) | The median OS of pembrolizumab arm (10.3 months) was significantly longer than that of the chemotherapy arm (7.4 months) | [6] |
Nivolumab | Opdivo | PD-1 | 3 mg/kg, every 2 weeks | 2 | Checkmate 275 | 270 | Confirmed ORR for all patients was 19.6%. Severe AEs (grade 3–4) occurred in 18% of patients | [9] |
Atezolizumab | Tecentriq | PD-L1 | 1200 mg, every 3 weeks | 3 | IMvigor211 | 931 (467 versus 464) | The median OS of the pre-stratified PD-L1 high expression patients (> 5%) did not differ significantly between the atezolizumab arm (11.1 months) and the chemotherapy arm (10.6 months) | [10] |
Durvalumab | Imfinzi | PD-L1 | 10 mg/kg, every 2 weeks | 1/2 | 191 | The overall ORR was 17.8% including 7% CR. Severe AEs (grade 3–4) and grade 3–4 immune-mediated AEs occurred in 6.8 and 2.1% of the patients, respectively | [11] | |
Avelumab | Bavencio | PD-L1 | 10 mg/kg, every 2 weeks | 1 | JAVELIN | 161 | The ORR was 17% including 6% with CR. Severe (grade 3–4) treatment-related AEs occurred in 8% | [12] |
PD-1 programmed death 1, PD-L1 programmed death ligand 1, OS overall survival, ORR objective response rate, CR complete response, AE adverse event, Reference the reference number in this review article