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Pexidartinib and standard neoadjuvant therapy in the adaptively randomized I-SPY2 trial for early breast cancer

  • Hope S. Rugo*
  • , Mike Campbell
  • , Christina Yau
  • , A. Jo Chien
  • , Anne M. Wallace
  • , Claudine Isaacs
  • , Judy C. Boughey
  • , Hyo S. Han
  • , Meredith Buxton
  • , Julia L. Clennell
  • , Smita M. Asare
  • , Katherine Steeg
  • , Amy Wilson
  • , Ruby Singhrao
  • , Jeffrey B. Matthews
  • , Jane Perlmutter
  • , W. Fraser Symmans
  • , Nola M. Hylton
  • , Angela M. DeMichele
  • , Douglas Yee
  • Laura J. van’t Veer, Donald A. Berry, Laura J. Esserman
*Corresponding author for this work
  • University of California at San Francisco
  • University of California at San Diego
  • Georgetown University
  • Mayo Clinic Rochester, MN
  • Moffitt Cancer Center
  • Quantum Leap Healthcare Collaborative
  • Gemini Group
  • University of Texas MD Anderson Cancer Center
  • University of Pennsylvania
  • University of Minnesota Twin Cities
  • LLC

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Purpose: We investigated the small-molecule receptor tyrosine kinase-inhibitor of colony-stimulating factor-1 receptor pexidartinib in the stage II/III breast cancer in the I-SPY2 platform trial. Methods: I-SPY2 is an adaptive platform trial that features multiple arms of experimental agents administered on a background of standard neoadjuvant therapy with paclitaxel and adriamycin/cyclophosphamide, followed by definitive surgery. The adaptive randomization engine preferentially assigns patients based upon cumulative performance of each agent in a given breast cancer subtype based on hormone receptor and HER2 receptor status. The study endpoint is pathologic complete response. Results: A total of 9 participants were randomized to receive pexidartinib with neoadjuvant paclitaxel before enrollment was halted due to a serious adverse event of vanishing bile duct syndrome. No participants received a full course of the study drug. Conclusion: Although there remains interest in agents targeting CSF-1, hepatic toxicity appears to be a limiting factor for their use in early breast cancer. Trial registration: NCT01042379 (www.clinicaltrials.gov/ct2/show/NCT01042379).
Original languageEnglish
Article number109844
JournalBreast cancer research and treatment
DOIs
Publication statusE-pub ahead of print - 2024
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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