Incidence of grade ≥ 3 DRAEs in patients from KEYNOTE-001 and KEYNOTE-006

AE, %Nonrandomized and randomized cohortsNSCLC cohortsKEYNOTE-006KEYNOTE- 006
(n = 411) [16](n = 495) [22](melanoma, 10 mg/kg Q2W, n = 278) [21](melanoma,10 mg/kg Q3W, n = 277) [21]
Fatigue2<10<1
ALT increase<1<10<1
Colitis<1NR13
Decreased appetite<1100
Diarrhea<1<131
Dyspnea<140<1
Headache<1NR00
Hepatitis<1NR12
Hyperthyroidism<1NR00
Hypophysitis<1NR<1<1
Hypothyroidism<1<1<10
Nausea<1<10<1
Pneumonitis<120<1
Pruritus<1000
Rash<1<100
Arthralgia0<10<1
Asthenia01<10

KEYNOTE-001 included melanoma and lung cohorts; KEYNOTE-006 included patients with melanoma

Numbers given as percentages where available

Abbreviations: AE adverse event; ALT alanine aminotransferase; DRAE drug-related AEs; NR not reported; NSCLC non-small cell lung cancer