Abstract 1777P
Background
The primary analysis of EMBARK demonstrated that after a median follow-up of 60.7 months metastasis-free survival for enza + leuprolide acetate (LA; HR 0.42; 95% CI, 0.30–0.61; p<0.0001) and enza monotherapy (HR 0.63; 95% CI, 0.46–0.87; p=0.0049) was clinically meaningful and statistically superior to placebo + LA. Here, we present other non-key secondary efficacy endpoints for enza monotherapy vs placebo + LA.
Methods
EMBARK (NCT02319837) is a phase 3 study of patients (pts) with high-risk BCR: prostate-specific antigen (PSA) doubling time ≤9 months and PSA ≥2 ng/mL above nadir post-radiotherapy (RT) or ≥1 ng/mL after radical prostatectomy (RP) ± postoperative RT. Pts were randomized (1:1) to 160 mg/day enza monotherapy (open-label) or placebo + LA (LA alone). LA 22.5 mg was administered every 12 weeks. If the PSA was <0.2 ng/mL at Week 36, tx was suspended at Week 37 and restarted when PSA was ≥2 ng/mL for pts with primary RP, and ≥5 ng/mL for pts without RP. Secondary endpoints included time to: distant metastasis, symptomatic progression, first symptomatic skeletal event, and resumption of any hormonal therapy following tx suspension.
Results
713 pts were eligible and randomized (enza monotherapy, n=355; LA alone, n=358). Median (range) tx duration excluding tx suspension was 45.9 (0.4–88.9) months for enza monotherapy and 35.4 (0.7–85.7) months for LA alone. Time to: distant metastasis (HR 0.61; 95% CI, 0.41–0.92; p=0.0171), symptomatic progression (HR 0.62; 95% CI, 0.49–0.79; p<0.0001), and first symptomatic skeletal event (HR 0.42; 95% CI, 0.23–0.79; p=0.0057) all favored enza monotherapy vs. LA alone. Time to resumption of any hormonal therapy after tx suspension favored LA alone vs enza monotherapy (HR 1.66; 95% CI, 1.38–1.98; p<0.0001). All p-values are nominal.
Conclusions
In pts with high-risk BCR, enza monotherapy showed clinically meaningful delays in time to distant metastasis, symptomatic progression, and time to first symptomatic skeletal event vs LA alone. After tx suspension, enza monotherapy shortened time to resumption of any hormonal therapy vs LA alone. Further work is needed to understand the risks and benefits of enza monotherapy vs other options for high-risk BCR.
Clinical trial identification
NCT02319837.
Editorial acknowledgement
Medical writing and editorial support were provided by Isabel Aitcheson, BSc, and Sinead Stewart of Onyx (a Prime Global agency), funded by Pfizer, Inc. and Astellas Pharma, Inc., co-developers of enzalutamide.
Legal entity responsible for the study
Pfizer, Inc. and Astellas Pharma, Inc.
Funding
Pfizer, Inc. and Astellas Pharma, Inc.
Disclosure
U.F.F. De Giorgi: Financial Interests, Personal, Advisory Board: Pfizer, BMS, MSD, PharmaMar, Astellas, Bayer, Ipsen, Novartis, Eisai, Janssen; Financial Interests, Personal, Invited Speaker: Roche, BMS, Clovis Oncology, AstraZeneca; Financial Interests, Institutional, Research Grant: AstraZeneca, Sanofi, Roche. S.J. Freedland: Financial Interests, Institutional, Speaker, Consultant, Advisor: Astellas Pharma Inc., Pfizer, Janssen, Bayer, Sanofi, Dendreon, Myovant, AstraZeneca, Merck. M.E. Gleave: Financial Interests, Institutional, Stocks or ownership: OncoGenex Technologies, Sustained Therapeutics, Sikta Pharmaceuticals; Financial Interests, Institutional, Speaker, Consultant, Advisor: Astellas Pharma Inc., AstraZeneca, Bayer, GDx, Janssen, Sanofi, Pfizer, TerSera, Roche; Financial Interests, Institutional, Other, Holds patents for OGX-011: OGX-011; Financial Interests, Institutional, Other, Holds patents for OGX-427: OGX-427; Financial Interests, Institutional, Other, Holds patents for ST-CP: ST-CP; Financial Interests, Institutional, Other, Holds patents for ST-POP: ST-POP. R. Tutrone: Financial Interests, Institutional, Advisory Board: Bayer; Financial Interests, Institutional, Speaker, Consultant, Advisor: Astellas Pharma Inc., Exosome Diagnostics GmbH, Myovant Sciences GmbH, Pfizer, Inc.. J.L. Bailen: Financial Interests, Institutional, Speaker, Consultant, Advisor, Consulting; honoraria; speaker's bureau: Astellas Pharma Inc., Auxillium, Bayer, Dendreon, Janssen; Financial Interests, Institutional, Speaker, Consultant, Advisor, Consulting and honoraria: Sanofi; Financial Interests, Institutional, Research Funding: Astellas Pharma Inc., Bayer, Dendreon, Janssen, Medivation, Millenium Pharmaceuticals; Financial Interests, Personal, Other, Travel, accommodation, and expenses: Astellas Pharma Inc., Bayer, Dendreon, Valeant/Dendreon. L.I. Karsh: Financial Interests, Institutional, Speaker, Consultant, Advisor: Astellas Pharma Inc., AstraZeneca, Aurora Oncology, Bayer, Daiichi Sankyo, Dendreon, Ferring, Janssen, Merck, Pfizer, Sanofi, Specialty Networks/UroGPO, Vaxiion; Financial Interests, Institutional, Speaker’s Bureau: Astellas Pharma Inc., AstraZeneca, Bayer, Janssen, Merck, Myovant Sciences, Pfizer; Financial Interests, Institutional, Research Funding: Astellas Pharma Inc., AstraZeneca, Bayer, BioExcel, BMS, Dendreon, Exact Sciences, Epizyme, FKD Therapies, KDX Pharma, Immunis.AI, Janssen, Merck, Myovant Sciences, Pfizer, Tavanta Therapeutics. M. Ramirez-Backhaus: Financial Interests, Institutional, Speaker, Consultant, Advisor, Consulting; honoraria: Astellas Pharma Inc., Bayer, Janssen; Financial Interests, Institutional, Expert Testimony: Janssen; Financial Interests, Personal, Other, Travel, accommodation, and expenses: Astellas Pharma Inc., Janssen. E. Uchio: Financial Interests, Institutional, Research Funding: Astellas Pharma Inc., AstraZeneca, Bayer, Blue Earth Diagnostics, CG Oncology, Dendreon Pharmaceuticals LLC, Exact Sciences, Lantheus, Myriad, Janssen Oncology, Merck, Myovant Sciences, Pfizer, Seagen; Financial Interests, Institutional, Speaker, Consultant, Advisor: Astellas Pharma Inc., AstraZeneca, Bayer, Blue Earth Diagnostics, CG Oncology, Dendreon Pharmaceuticals LLC, Exact Sciences, Lantheus, Myriad, Janssen Oncology, Merck, Myovant Sciences, Pfizer, Seagen. S. Supiot: Financial Interests, Institutional, Other, Honoraria: Astellas Pharma Inc., AstraZeneca, Bayer, Ferring, Ipsen, Janssen, Merck Sharp & Dohme, Novartis AAA, Takeda; Financial Interests, Institutional, Research Funding: Astellas Pharma, Inc., AstraZeneca, Bayer, Boston Scientific, Janssen, Novartis AAA, RefleXion Medical. Y. Tang, B. Rosbrook: Financial Interests, Personal, Full or part-time Employment: Pfizer; Financial Interests, Personal, Stocks/Shares: Pfizer. G.P. Haas, M. Rosales: Financial Interests, Personal, Full or part-time Employment: Astellas Pharma, Inc.; Financial Interests, Personal, Stocks/Shares: Astellas Pharma, Inc.. F. Zohren: Financial Interests, Personal, Full or part-time Employment: Pfizer, Inc.; Financial Interests, Personal, Stocks/Shares: Pfizer, Inc.. N.D. Shore: Financial Interests, Institutional, Other, Grant support and consulting fees: AbbVie, Amgen, Astellas Pharma Inc., AstraZeneca, Bayer, Clovis Oncology, Dendreon Pharmaceuticals LLC, Ferring Pharmaceuticals, GenesisCare, Janssen Oncology, Merck, Myovant Sciences, Pfizer, Sanofi-Genzyme, Tolmar Pharmaceuticals. All other authors have declared no conflicts of interest.
Resources from the same session
1807P - Talazoparib (TALA) plus enzalutamide (ENZA) in metastatic castration-resistant prostate cancer (mCRPC): Subgroup analyses of the all-comers cohort from TALAPRO-2 by homologous recombination repair (HRR) status
Presenter: Nobuaki Matsubara
Session: Poster session 14
1808P - Pain response and health-related quality of life (HRQL) analysis in patients with metastatic castration-resistant prostate cancer (mCRPC) receiving cabazitaxel every 2 weeks (16 mg/m<sup>2</sup>) versus every 3 weeks (25 mg/m<sup>2</sup>) in the CABASTY phase III trial
Presenter: Stephane Oudard
Session: Poster session 14
1809P - Dynamics of plasma tumour DNA and copy number alterations in advanced metastatic castration-resistant prostate cancer (mCRPC) patients treated with cabazitaxel: A prospective biomarker trial
Presenter: Nicole Brighi
Session: Poster session 14
1810P - Association of health-related quality of life with efficacy outcomes in the VISION study of patients with metastatic castration-resistant prostate cancer
Presenter: Michael Morris
Session: Poster session 14
1811P - Patient-reported outcomes (PROs) in men with metastatic castration-resistant prostate cancer (mCRPC) and homologous recombination repair (HRR) mutations receiving talazoparib (TALA) + enzalutamide (ENZA) vs placebo (PBO) + ENZA: Results from a phase III (TALAPRO-2) study
Presenter: Andre Fay
Session: Poster session 14
1813P - Phase I/II trial of oral EPI-7386 in combination with enzalutamide (enz) compared to enz alone in metastatic castration-resistant prostate cancer (mCRPC) subjects: Current phase I (PI) results
Presenter: Andrew Laccetti
Session: Poster session 14
1814P - First real-life data on [177Lu]Lu-PSMA-617: Descriptive analysis on the largest metastatic castration-resistant prostate cancer (mCRPC) cohort treated in early access in France
Presenter: Anne-Laure Giraudet
Session: Poster session 14
1815P - Emergent circulating tumor DNA (ctDNA) variants and ctDNA burden dynamics with potential associations with talazoparib antitumor activity in TALAPRO-1
Presenter: Elena Castro
Session: Poster session 14