Talazoparib plus enzalutamide in metastatic castration-resistant prostate cancer: TALAPRO-2 phase III study design

Author:

Agarwal Neeraj1ORCID,Azad Arun2ORCID,Shore Neal D3ORCID,Carles Joan4ORCID,Fay Andre P5,Dunshee Curtis6ORCID,Karsh Lawrence Ivan7ORCID,Paccagnella Maria Luisa8,Santo Nicola Di9,Elmeliegy Mohamed10ORCID,Lin Xun10,Czibere Akos11,Fizazi Karim12

Affiliation:

1. Huntsman Cancer Institute (NCI-CCC), University of Utah, Salt Lake City, UT 84112, USA

2. Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria, 3000, Australia

3. Department of Urology, Carolina Urologic Research Center, Myrtle Beach, SC 29572, USA

4. Vall d'Hebron University Hospital, Vall d'Hebron Institute of Oncology (VHIO), Barcelona , 08035, Spain

5. PUCRS School of Medicine Grupo Oncoclínicas, Porto Alegre , 90610-000, Brazil

6. Urological Associates of Southern Arizona, Tucson, AZ 85741, USA

7. The Urology Center of Colorado, Denver, CO 80211, USA

8. Pfizer Inc., Global Product Development, Groton, CT 06340, USA

9. Pfizer Inc., Global Product Development, Durham, NC 27707, USA

10. Pfizer Inc., Global Product Development, La Jolla, CA 92121, USA

11. Pfizer Inc., Cambridge, MA, USA

12. Department of Cancer Medicine, Institut Gustave Roussy, University of Paris Saclay, Villejuif, 94800, France

Abstract

PARP inhibitors in combination with androgen receptor-targeted therapy have demonstrated potential in the treatment of metastatic castration-resistant prostate cancer (mCRPC). Here, we describe the design and rationale of the multinational, phase III, two-part TALAPRO-2 study comparing talazoparib plus enzalutamide versus placebo plus enzalutamide as a first-line treatment for patients with mCRPC with or without DNA damage response (DDR) alterations. This study has two co-primary end points: radiographic progression-free survival (rPFS) by blinded independent clinical review in all-comers (cohort 1) and in patients with DDR alterations (cohort 2). TALAPRO-2 will demonstrate whether talazoparib plus enzalutamide can significantly improve the efficacy of enzalutamide in terms of rPFS in both molecularly unselected and DDR-deficient patients with mCRPC (NCT03395197). Clinical Trial Registration: NCT03395197  (ClinicalTrials.gov).

Funder

Pfizer

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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