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Entinostat, nivolumab and ipilimumab for women with advanced HER2-negative breast cancer: a phase Ib trial

  • Evanthia.T. Roussos Torres,
  • Won J. Ho,
  • Ludmila Danilova,
  • Joseph A. Tandurella,
  • James Leatherman,
  • Christine Rafie,
  • Chenguang Wang,
  • Adam Brufsky,
  • Patricia LoRusso,
  • Vincent Chung,
  • Yuan Yuan,
  • Melinda Downs,
  • Ashley O’Connor,
  • Sarah M. Shin,
  • Alexei Hernandez,
  • Elizabeth L. Engle,
  • Richard Piekarz,
  • Howard Streicher,
  • Zahra Talebi,
  • Michelle A. Rudek,
  • Qingfeng Zhu,
  • Robert A. Anders,
  • Ashley Cimino-Mathews,
  • Elana J. Fertig,
  • Elizabeth M. Jaffee,
  • Vered Stearns,
  • Roisin M. Connolly

摘要

We report the results of 24 women, 50% (N = 12) with hormone receptor-positive breast cancer and 50% (N = 12) with advanced triple-negative breast cancer, treated with entinostat + nivolumab + ipilimumab from the dose escalation (N = 6) and expansion cohort (N = 18) of ETCTN-9844 (NCT02453620). The primary endpoint was safety. Secondary endpoints were overall response rate, clinical benefit rate, progression-free survival and change in tumor CD8:FoxP3 ratio. There were no dose-limiting toxicities. Among evaluable participants (N = 20), the overall response rate was 25% (N = 5), with 40% (N = 4) in triple-negative breast cancer and 10% (N = 1) in hormone receptor-positive breast cancer. The clinical benefit rate was 40% (N = 8), and progression-free survival at 6 months was 50%. Exploratory analyses revealed that changes in myeloid cells may contribute to responses; however, no correlation was noted between changes in CD8:FoxP3 ratio, PD-L1 status and tumor mutational burden and response. These findings support further investigation of this treatment in a phase II trial.