“…Phased ipilimumab, concurrent ipilimumab and control, respectively, were associated with median median PFS of 5.2, 3.9 and 5.2 months; median OS of 12.9, 9.1 and 9.9 months. Overall rates of grade 3/4 irAEs (immun-related advers events) were 17, 21 and 9% for phased ipilimumab, concurrent ipilimumab and control, respectively [14]. A phase 3 trial comparing the efficacy of ipilimumab plus etoposide/platinum versus etoposide/platinum in patients with newly diagnosed ED-SCLC (NCT01450761) is currently ongoing.…”