Tetrathiomolybdate-associated copper depletion decreases circulating endothelial progenitor cells in women with breast cancer at high risk of relapse

  • S. Jain
  • , J. Cohen
  • , M. M. Ward
  • , N. Kornhauser
  • , E. Chuang
  • , T. Cigler
  • , A. Moore
  • , D. Donovan
  • , C. Lam
  • , M. V. Cobham
  • , S. Schneider
  • , Sandra Hurtado Rua
  • , S. Benkert
  • , C. Mathijsen Greenwood
  • , R. Zelkowitz
  • , J. D. Warren
  • , M. E. Lane
  • , V. Mittal
  • , S. Rafii
  • , L. T. Vahdat

Research output: Contribution to journalArticlepeer-review

95 Scopus citations

Abstract

Background: Bone marrow-derived endothelial progenitor cells (EPCs) are critical for metastatic progression. This study explores the effect of tetrathiomolybdate (TM), an anti-angiogenic copper chelator, on EPCs in patients at high risk for breast cancer recurrence. Patients and methods: This phase 2 study enrolled breast cancer patients with stage 3 and stage 4 without evidence of disease (NED), and stage 2 if triple-negative. TM 100 mg orally was administered to maintain ceruloplasmin <17 mg/dl for 2 years or until relapse. The primary end point was change in EPCs. Results: Forty patients (28 stage 2/3, 12 stage 4 NED) were enrolled. Seventy-five percent patients achieved the copper depletion target by 1 month. Ninety-one percent of triple-negative patients copper-depleted compared with 41% luminal subtypes. In copper-depleted patients only, there was a significant reduction in EPCs/ml by 27 (P = 0.04). Six patients relapsed while on study, of which only one patient had EPCs maintained below baseline. The 10-month relapse-free survival was 85.0% (95% CI 74.6%-96.8%). Only grade 3/4 toxicity was hematologic: neutropenia (3.1% of cycles), febrile neutropenia (0.2%), and anemia (0.2%). Conclusions: TM is safe and appears to maintain EPCs below baseline in copper-depleted patients. TM may promote tumor dormancy and ultimately prevent relapse. © The Author 2013.Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved.
Original languageEnglish
Pages (from-to)1491-1498
Number of pages8
JournalAnnals of Oncology
Volume24
Issue number6
DOIs
StatePublished - Jan 1 2013

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

Keywords

  • Breast cancer
  • Endothelial progenitor cells
  • Tetrathiomolybdate

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