DRAEs with incidence ≥5 % observed in patients from KEYNOTE-001 and KEYNOTE-006

AE, %Nonrandomized and randomized cohorts KEYNOTE-001NSCLC cohorts KEYNOTE-001KEYNOTE-006KEYNOTE-006
(n = 411) [16](n = 495) [22](melanoma, 10 mg/kg Q2W, n = 278) [21](melanoma, 10 mg/kg Q3W, n = 277) [21]
Fatigue36192119
Pruritus24111414
Rash20101513
Arthralgia169912
Diarrhea1681714
Nausea1281011
Vitiligo11NR911
Asthenia951211
Cough9244
Myalgia9372
Headache8232
Hypothyroidism87109
Decreased appetite71167
Dyspnea7413
Chills6210
Pyrexia6441
ALT increase5241
Pneumonitis34<12
Hyperthyroidism1273
Colitis<1NR24
Hepatitis<1NR12
HypophysitisNRNR<1<1
NephritisNRNR0<1

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; DRAEs drug-related AEs; NR not reported; NSCLC non-small cell lung cancer