AstraZeneca Investor Day Presentation Deck slide image

AstraZeneca Investor Day Presentation Deck

PROpel - unprecedented clinical benefit without compromising quality of life - a potential new SoC in mCRPC Outcomes remain poor in advanced prostate cancer 40% of patients with prostate cancer will develop metastatic disease ¹-3 30% the 5-year survival rate for patients with metastatic disease4 3 years median OS for mCRPC patients in the first-line setting 5-9 50% of patients receive only one line of active therapy in mCRPC10 ● ● ● ● PROpel building on the success of PROfound Representative real-world population - simple trial design All-comers ITT population Retrospective HRR testing via tissue and ctDNA testing¹¹ Primary endpoint: radiographic progression free survival Key secondary endpoints: Overall survival, time to first subsequent therapy, time to second progression or death ● 300 Lynparza™ + abiraterone mg olaparib a potential new standard of care Clinically meaningful and consistent efficacy across subgroups Despite OS immaturity, strong secondary endpoint results provide confidence Class-leading tolerability - full 300mg Lynparza dose in combination with abiraterone Quality of life maintained, allowing adoption of upfront combination therapy 8.2-month median rPFS benefit over abiraterone alone 1. Beltran H, Beer TM, Carducci MA, et al. Eur Urol. 2011;60(2):279-290. 2. Sciarra A, Salciccia S. Eur Urol. 2014;65(5):905-906. 3. Sartor O, de Bono JS. N Engl J Med. 2018;378(7):645-657.4. Cancer of the Prostate - Cancer Stat Facts. SEER. Accessed November 6, 2019. 5. Kelly WK et al. J Clin Oncol. 2012;30:1534-40. 6. Quinn DI et al. Lancet Oncol. 2013;14:893-900. 7. Araujo JC et al. Lancet Oncol. 2013;14:1307-16.8. Ryan CJ et al. N Engl J Med. 2013;368:138-48.9. Beer TM et al. N Engl J Med. 2014;371:424-33. 10. Shore ND et al. Adv Ther. 2021;38:4520-40. 11. Tumour tissue and blood samples were collected at baseline for biomarker tests. HRRm status was determined 23 using a tumour tissue test (Foundation One® CDX) and/or a circulating tumour (ctDNA) based test (FoundationOneⓇLiquid CDx test). OS = overall survival; ITT = intent-to-treat.
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