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Table 2 Efficacy and safety of osimertinib in clinical trials

From: Therapeutic strategies for EGFR-mutated non-small cell lung cancer patients with osimertinib resistance

Trial

Phase

Number of patients

ORR

(%)

PFS

(months)

OS

(months)

AEs of osimertinib treatment

AURA

(NCT01802632)

1/2

253

61

9.6

/

Diarrhea (47%), rash (40%), nausea (22%), decreased appetite (21%)

AURA extension

2

201

62

12.3

/

Diarrhea (43%), rash (40%), dry skin (31%), paronychia (31%)

AURA2

(NCT02094261)

2

210

70

9.9

/

Rash (41%), diarrhea (33%), dry skin (30%), paronychia (26%)

AURA extension

and AURA2

2

411

66

9.9

26.8

Rash (42%), diarrhea (39%), dry skin (32%), paronychia (32%)

AURA3

(NCT02151981)

3

279

71

10.1

26.8

Diarrhea (41%), rash (34%), dry skin (23%), paronychia (22%)

FLAURA

(NCT02296125)

3

279

80

18.9

38.6

Rash (58%), diarrhea (58%), dry skin (36%), paronychia (35%)

ADAURA (NCT02511106)

3

682

57.1

NR*

(38.8-NC)

Awaited

Diarrhea (46%), paronychia (25%), dry skin (23%), pruritus (19%)

  1. ORR objective response rate, PFS progression-free survival, OS overall survival, AEs adverse events, NR not reached, NC could not be calculated
  2. *represents disease-free survival (DFS)