4.5 Article

The safety and tolerability of epacadostat alone and in combination with pembrolizumab in patients with advanced solid tumors: results from a first-in-Japanese phase I study (KEYNOTE-434)

Journal

INVESTIGATIONAL NEW DRUGS
Volume 39, Issue 1, Pages 152-162

Publisher

SPRINGER
DOI: 10.1007/s10637-020-00942-1

Keywords

Advanced solid tumors; Epacadostat (INCB024360); Japanese; Pembrolizumab

Funding

  1. Merck Sharp Dohme Corp.
  2. Incyte Corporation, Wilmington, DE, USA

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The open-label, phase I KEYNOTE-434 study evaluated the safety and tolerability of epacadostat alone and in combination with pembrolizumab in Japanese patients with advanced solid tumors. Results showed that the combination therapy was generally safe and well tolerated, with potential therapeutic benefits for this patient population.
Purpose Part A of the open-label, phase I KEYNOTE-434 study evaluated the safety and tolerability of epacadostat, an indoleamine 2,3-dioxygenase-1 inhibitor, alone and in combination with pembrolizumab in Japanese patients with advanced solid tumors. Methods Japanese patients with refractory/recurrent metastatic or locally advanced tumors were enrolled. Cohort 1 received oral epacadostat 25 mg or 100 mg twice daily (BID) and subsequently received epacadostat in combination with intravenous pembrolizumab 200 mg every 3 weeks. Cohort 2 received epacadostat 25 mg or 100 mg BID with pembrolizumab 200 mg every 3 weeks. The primary objective was evaluation of safety and tolerability using a modified toxicity probability interval method. Secondary objectives were pharmacokinetic (PK) and pharmacodynamic profiles of epacadostat alone and in combination with pembrolizumab. Results Six patients were enrolled in cohort 1 (epacadostat 25 mg,n = 3; epacadostat 100 mg,n = 3); none experienced dose-limiting toxicities (DLTs). Nine patients were enrolled in cohort 2 (epacadostat 25 mg and pembrolizumab,n = 3; epacadostat 100 mg and pembrolizumab,n = 6); one patient receiving epacadostat 100 mg and pembrolizumab experienced grade 4 rhabdomyolysis-a DLT. Grade 3 or 4 treatment-related adverse events occurred in two patients (13.3%). There were no treatment-related deaths. Pembrolizumab had no impact on epacadostat PK and vice versa. The PK profile of pembrolizumab in the current study was comparable with historical pembrolizumab PK data. Conclusion Epacadostat in combination with pembrolizumab was generally safe and well tolerated among Japanese patients with advanced solid tumors. Clinical trial registrationNCT02862457.

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