Cited by 325Cancer Immunotherapy and BiomarkersImmunotherapy and Immune ResponsesTryptophan and brain disorders

First-in-human phase I study of the oral inhibitor of indoleamine 2,3-dioxygenase-1 epacadostat (INCB024360) in patients with advanced solid malignancies

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Beatty, Gregory L., O'Dwyer, Peter J., Clark, Jason, Shi, Jack G., Bowman, Kevin J., Scherle, Peggy A., Newton, Robert C., Schaub, Richard +3 more·2017·Clinical Cancer Research

Abstract

Abstract Purpose: Indoleamine 2,3-dioxygenase-1 (IDO1) catalyzes the degradation of tryptophan to N-formyl-kynurenine. Overexpressed in many solid malignancies, IDO1 can promote tumor escape from host immunosurveillance. This first-in-human phase I study investigated the maximum tolerated dose, safety, pharmacokinetics, pharmacodynamics, and antitumor activity of epacadostat (INCB024360), a potent and selective inhibitor of IDO1. Experimental Design: Fifty-two patients with advanced solid malignancies were treated with epacadostat [50 mg once daily or 50, 100, 300, 400, 500, 600, or 700 mg twice daily (BID)] in a dose-escalation 3 + 3 design and evaluated in 28-day cycles. Treatment was continued until disease progression or unacceptable toxicity. Results: One dose-limiting toxicity (DLT) occurred at the dose of 300 mg BID (grade 3, radiation pneumonitis); another DLT occurred at 400 mg BID (grade 3, fatigue). The most common adverse events in >20% of patients overall were fatigue, nausea, decreased appetite, vomiting, constipation, abdominal pain, diarrhea, dyspnea, back pain, and cough. Treatment produced significant dose-dependent reductions in plasma kynurenine levels and in the plasma kynurenine/tryptophan ratio at all doses and in all patients. Near maximal changes were observed at doses of ≥100 mg BID with >80% to 90% inhibition of IDO1 achieved throughout the dosing period. Although no objective responses were detected, stable disease lasting ≥16 weeks was observed in 7 of 52 patients. Conclusions: Epacadostat was generally well tolerated, effectively normalized kynurenine levels, and produced maximal inhibition of IDO1 activity at doses of ≥100 mg BID. Studies investigating epacadostat in combination with other immunomodulatory drugs are ongoing. Clin Cancer Res; 23(13); 3269–76. ©2017 AACR.

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Authors
Beatty, G. L., O'Dwyer, P. J., Clark, J., Shi, J. G., Bowman, K. J., Scherle, P. A., Newton, R. C., Schaub, R., Maleski, J., Leopold, L., & Gajewski, T. F.
Affiliations
  • Abramson Cancer Center (US)
  • Incyte (United States) (US)
  • University of Chicago (US)
Corresponding author
Beatty, Gregory L.
Venue
Clinical Cancer Research
Published
2017-07-01
Volume
23
Issue
13
Pages
3269-3276
ISSN
  • 1078-0432 (ISSN-L)
  • 1557-3265
OpenAlex
W2570766240
Cited by
314
References
40
Citations by year
2026: 14 · 2025: 18 · 2024: 42 · 2023: 21 · 2022: 26 · 2021: 36 · 2020: 33 · 2019: 44 · 2018: 53 · 2017: 24 · 2016: 1 · 2014: 2
FWCI
18.80
Type
journal article
Language
en
Open access
Locations
  • Clinical Cancer Research (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • University of Chicago
  • Abramson Cancer Center
  • National Cancer Institute (K08CA138907)
Topics
  • Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
  • Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
  • Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
Keywords
epacadostat, IDO1, IDO1 inhibitors, advanced solid tumors, kynurenine, kynurenine/tryptophan ratio, tryptophan degradation, tumor immunosuppression, radiation pneumonitis, dose-limiting toxicity, pharmacokinetics, pharmacodynamics, anticancer activity, maximum tolerated dose
MeSH terms
Administration, Oral, Adult, Aged, Dose-Response Relationship, Drug, Drug Administration Schedule, Female, Humans, Male, Middle Aged, Neoplasm Staging, Neoplasms, Oximes, Sulfonamides, Indoleamine-Pyrrole 2,3,-Dioxygenase, Drug-Related Side Effects and Adverse Reactions

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