Pembrolizumab in patients with previously treated advanced hepatocellular carcinoma: Phase 2 KEYNOTE-224 study

Date

08 Oct 2016

Session

Poster Display

Presenters

Andrew Zhu

Citation

Annals of Oncology (2016) 27 (6): 207-242. 10.1093/annonc/mdw371

Authors

A. Zhu1, J. Knox2, M. Kudo3, S. Chan4, R. Finn5, A. Siegel6, J. Ma7, P.A. Watson6, A. Cheng8

Author affiliations

  • 1 Medical Oncology, Massachusetts General Hospital, 02114 - Boston/US
  • 2 Princess Margaret Cancer Centre, University of Toronto, Toronto/CA
  • 3 Medicine, Kinki University School of Medicine, Osaka/JP
  • 4 Medical Oncology, Prince of Wales Hospital, Shatin/HK
  • 5 Medicine, University of California, Los Angeles, 90404 - Los Angeles/US
  • 6 Medical Oncology, Merck & Co, Inc., Kenilworth/US
  • 7 Medical Oncology, Merck & Co., Inc., Kenilworth/US
  • 8 Graduate Institute Of Oncology, National Taiwan University Hospital, 100 - Taipei/TW
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Background

Liver cancer is the second leading cause of cancer deaths worldwide. The tyrosine kinase inhibitor sorafenib is the standard of care for first-line hepatocellular carcinoma (HCC), and there is currently no clear standard of care for second-line HCC. Because most HCC is driven by inflammation, there is a strong rationale to evaluate immunotherapy in patients with this type of cancer. The single-arm, multisite, phase 2 KEYNOTE-224 study (ClinicalTrials.gov, NCT02702414) was designed to evaluate the efficacy and safety of the anti–PD-1 antibody pembrolizumab in patients with previously treated advanced HCC.

Trial design

Approximately 100 patients will be enrolled. Inclusion criteria include age ≥18 years, histologically or cytologically confirmed diagnosis of HCC, documented objective radiographic progression after stopping treatment with sorafenib or intolerance to sorafenib, and disease not amenable to a curative treatment approach (eg, transplantation, surgery, or ablation). Patients must also have measurable disease confirmed by central imaging vendor per RECIST v1.1, Child-Pugh liver score A, ECOG performance status 0-1, and predicted life expectancy >3 months. Patients will be allocated to receive pembrolizumab 200 mg IV Q3W for up to 35 cycles (∼2 years) or until disease progression, unacceptable toxicity, or investigator decision. Response will be assessed every 9 weeks per RECIST v1.1 by central imaging vendor review. Adverse events (AEs) will be assessed throughout treatment and for 30 days thereafter (90 days for serious AEs) and graded per NCI CTCAE v4.0. The primary end point is objective response rate per RECIST v1.1 by central imaging vendor review. Secondary end points are duration of response, disease control rate, time to progression, and progression-free survival per RECIST v1.1 by central imaging vendor review; overall survival; and safety and tolerability.

Clinical trial identification

NCT02702414

Legal entity responsible for the study

Merck & Co., Inc.

Funding

Merck & Co., Inc.

Disclosure

M. Kudo: Lecture fee from Bayer Co.

S. Chan: Advisory Board Member: Novartis; Merck Corporate-Sponsored research: Novartis, Celgene, Eli Lilly, SIRTeX, AB Science, Merck, Medimmune.

R. Finn: Consultant: Pfizer, Merck, Bayer, Novartis, Bristol Meyers Squibb.

A. Siegel: Employee, stockholder Merck & Co., Inc.

J. Ma: Employee, stockholder: Merck & Co., Inc.

P.A. Watson: Employee and Stockholder, Merck & Co., Inc.

All other authors have declared no conflicts of interest.

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