AstraZeneca Investor Day Presentation Deck slide image

AstraZeneca Investor Day Presentation Deck

Imfinzi in Stage III, unresectable non-small cell lung cancer Cementing leadership in this potentially curative setting PACIFIC-R: Real world PFS Imfinzi after CRT for a median duration of ~11 months is effective in a large, real-world cohort of patients with unresectable Stage III NSCLC PFS Total events, N (%) Progression per RECIST Progression per physician assessment Progression, assessment unknown Deaths in absence of progression Median PFS, months 95% CI PFS rate, % 12 months 24 months PACIFIC-R FAS N=1,399 737 (52.7) 456 (32.6) 170 (12.2) 30 (2.1) 81 (5.8) 21.7 19.2-24.5 62.4 48.2 PACIFIC trial (durva. arm)¹ N=476 268 (56.3)* 16.9 13.0-23.9 55.7 45.0 1. Spigel DR, et al. J Clin Oncol 2021;39(15_suppl):8511. *Range for median follow-up duration = 0-35.6 months; *In the PACIFIC trial, PFS was assessed by BICR per RECIST v1.1; * Per local regulations. FAS, full analysis set; rw, real-world; UK, United Kingdom. 25 PFS probability COAST: PFS by investigator's analysis First randomised Phase II to show evidence of improved outcomes with novel 10 combinations in the PACIFIC setting 1.0 0.9 0.8 0.7 765432 0.6 0.5 o o o o 0.4 0.3 0.2 0.1 0 No. at risk D O. 0 67 60 D+O D+M 62 T 2 50 49 55 4 32 46 46 Events/patients, n mPFS, months (95% CI)¹ HR (95% CI)2,3 32 40 44 20 37 41 D 38/67 6.3 (3.7-11.2) 72.7% 6 8 10 Time from randomisation (months) 16 30 35 64.8% 39.2% T 12 14 13 22 25 9 13 11 H||| T 16 D+O 22/60 NR (10.4-NE) 0.44 (0.26-0.75) 7 9 6 T 18 3 5 1 20 0 0 1 D+M 21/62 15.1 (13.6-NE) 0.65 (0.49-0.85) Data cut-off: 17 May 2021 (median follow-up of 11.5 months; range, 0.4-23.4) D, durvalumab; M, monalizumab; O, oleclumab. 1. Interim analysis performed when all patients had a 10mth min potential follow-up; Kaplan-Meier estimates for PFS, PFS rate and 95% Cls 2. PFS HR and 95% CI estimated by Cox regression model, stratified by histology (adenocarcinoma and non- adenocarcinoma) 3. Compared with the 67 and 64 patients in the D arm enrolled concurrently with patients in the D+O and D+M arms, respectively.
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