Phase II trial of sorafenib in advanced salivary adenoid cystic carcinoma of the head and neck

  • David J. Thomson
    Department of Clinical Oncology The Christie NHS Foundation Trust Manchester United Kingdom
  • Priyamal Silva
    Department of Surgery The Christie NHS Foundation Trust Manchester United Kingdom
  • Kim Denton
    Department of Clinical Oncology The Christie NHS Foundation Trust Manchester United Kingdom
  • Suzanne Bonington
    Department of Radiology The Christie NHS Foundation Trust Manchester United Kingdom
  • Soo K. Mak
    Department of Radiology The Christie NHS Foundation Trust Manchester United Kingdom
  • Ric Swindell
    Department of Medical Statistics The Christie NHS Foundation Trust Manchester United Kingdom
  • Jarrod Homer
    Department of Surgery The Christie NHS Foundation Trust Manchester United Kingdom
  • Andrew J. Sykes
    Department of Clinical Oncology The Christie NHS Foundation Trust Manchester United Kingdom
  • Lip W. Lee
    Department of Clinical Oncology The Christie NHS Foundation Trust Manchester United Kingdom
  • Beng K. Yap
    Department of Clinical Oncology The Christie NHS Foundation Trust Manchester United Kingdom
  • Nicholas J. Slevin
    Department of Clinical Oncology The Christie NHS Foundation Trust Manchester United Kingdom

説明

<jats:title>Abstract</jats:title><jats:sec><jats:title>Background</jats:title><jats:p>There is a need to improve the systemic treatment of advanced adenoid cystic carcinoma (ACC). Response rates to chemotherapy are poor and preliminary investigations of molecularly targeted agents have been disappointing. In this study, we evaluate sorafenib, an oral multikinase inhibitor, which has an attractive targeting profile for this disease.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>In a single‐arm phase II trial, patients with unresectable locally recurrent and/or metastatic ACC were treated with sorafenib 400 mg bid.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Twenty‐three patients, median age 51 years, were recruited from 2009 to 2011. Median progression‐free survival (PFS) and overall survival (OS) were 11.3 and 19.6 months, respectively. PFS at 6 and 12 months were 69.3% and 46.2%, respectively. Sorafenib was only reasonably well tolerated, and 13 patients (57%) experienced grade 3 toxicity.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>Sorafenib showed modest activity in ACC with a 12‐month PFS of 46.2%. Sorafenib 400 mg bid was associated with significant toxicity and, taken together with limited effectiveness, cannot be enthusiastically recommended for further evaluation. © 2014 Wiley Periodicals, Inc. <jats:italic>Head Neck</jats:italic> <jats:bold>37</jats:bold>: 182‐187, 2015</jats:p></jats:sec>

収録刊行物

  • Head & Neck

    Head & Neck 37 (2), 182-187, 2014-03-13

    Wiley

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