Phase 3 Study of Talazoparib Plus Enzalutamide Versus Placebo Plus Enzalutamide as First-Line Treatment in Patients With Metastatic Castration-Resistant Prostate Cancer: TALAPRO-2 Japanese Subgroup Analysis

Cancer Med. 2025 Jan;14(1):e70333. doi: 10.1002/cam4.70333.

Abstract

Background: In TALAPRO-2, the poly(ADP-ribose) polymerase inhibitor talazoparib plus the androgen receptor-signaling inhibitor enzalutamide improved radiographic progression-free survival (rPFS) versus placebo plus enzalutamide (hazard ratio [HR] = 0.63; 95% CI, 0.51-0.78) in molecularly unselected patients with metastatic castration-resistant prostate cancer (mCRPC). We report an exploratory analysis of efficacy, safety, and pharmacokinetics in Japanese patients enrolled in the TALAPRO-2 study.

Methods: The ongoing, multinational, randomized, double-blind, phase 3 TALAPRO-2 study enrolled patients with mCRPC receiving ongoing androgen deprivation therapy. Patients were prospectively assessed for homologous recombination repair (HRR) gene alterations and randomized 1:1 to receive talazoparib or placebo plus enzalutamide once daily. The primary endpoint was rPFS by blinded independent central review (BICR). Secondary endpoints included overall survival, objective response, safety, and pharmacokinetics.

Results: For the 116 Japanese all-comers patients enrolled in TALAPRO-2, the HR for rPFS was 0.89 (95% CI, 0.45-1.75) for the talazoparib versus placebo arm; among those with HRR-deficient disease, the HR was 0.58 (95% CI, 0.16-2.20). Among patients with BRCA1/2 gene alterations in the HRR-deficient population (n = 10), the HR for rPFS was < 0.01 (95% CI, < 0.01-not reached) for the talazoparib versus placebo arm. In the all-comers population, the objective response rate by BICR was 55% (all complete responses) in the talazoparib arm versus 36% in the placebo arm. The safety profile of talazoparib plus enzalutamide was similar between Japanese patients and the overall all-comers population; no new safety signals were identified. Anemia was the most common grade 3/4 treatment-emergent adverse event (55%) and cause of talazoparib discontinuation (12%). Talazoparib Ctrough was comparable across Japanese, Asian, and non-Asian subgroups.

Conclusions: In this exploratory analysis, efficacy outcomes with talazoparib plus enzalutamide in Japanese patients in TALAPRO-2 were consistent with those in the overall all-comers population. The safety profile and pharmacokinetics of the combination were similar between Japanese patients and the overall all-comers population.

Trial registration: ClinicalTrials.gov Identifier: NCT03395197.

Keywords: Japanese; PARP inhibitor; TALAPRO‐2; enzalutamide; mCRPC; talazoparib.

Publication types

  • Randomized Controlled Trial
  • Clinical Trial, Phase III
  • Multicenter Study

MeSH terms

  • Aged
  • Aged, 80 and over
  • Antineoplastic Combined Chemotherapy Protocols* / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols* / therapeutic use
  • Benzamides* / administration & dosage
  • Benzamides* / therapeutic use
  • Double-Blind Method
  • East Asian People
  • Humans
  • Japan
  • Male
  • Middle Aged
  • Nitriles* / therapeutic use
  • Phenylthiohydantoin* / administration & dosage
  • Phenylthiohydantoin* / adverse effects
  • Phenylthiohydantoin* / analogs & derivatives
  • Phenylthiohydantoin* / therapeutic use
  • Phthalazines* / administration & dosage
  • Phthalazines* / adverse effects
  • Phthalazines* / pharmacokinetics
  • Phthalazines* / therapeutic use
  • Poly(ADP-ribose) Polymerase Inhibitors / administration & dosage
  • Poly(ADP-ribose) Polymerase Inhibitors / adverse effects
  • Poly(ADP-ribose) Polymerase Inhibitors / therapeutic use
  • Progression-Free Survival
  • Prostatic Neoplasms, Castration-Resistant* / drug therapy
  • Prostatic Neoplasms, Castration-Resistant* / mortality
  • Prostatic Neoplasms, Castration-Resistant* / pathology

Substances

  • talazoparib
  • Nitriles
  • Phthalazines
  • Benzamides
  • enzalutamide
  • Phenylthiohydantoin
  • Poly(ADP-ribose) Polymerase Inhibitors

Associated data

  • ClinicalTrials.gov/NCT03395197

Grants and funding