A pilot trial of suramin in metastatic breast cancer to assess antiangiogenic activity in individual patients

William J. Gradishar*, Gerald Soff, Jiangou Liu, Angela Cisneros, Suzanne French, Alfred Rademaker, Al B. Benson, Noel Bouck

*Corresponding author for this work

Research output: Contribution to journalArticle

17 Scopus citations

Abstract

Suramin is a polysulfonated naphthylurea with multiple potential mechanisms of action against tumors, including the ability to bind growth factors known to promote tumor angiogenesis. Using an established fixed dosing scheme for the administration of suramin in patients, a pilot study was conducted in patients with progressive, metastatic breast cancer. The primary objective of this trial is to define the effect of suramin on the angiogenic activity in individual patients using in vitro laboratory assays. The secondary objective was to assess the antitumor effect of suramin in a population of metastatic breast cancer patients. No objective tumor responses were observed in any of the 9 patients who received treatment with suramin, however 1 patient did maintain stable disease status. The strength of angiogenic activity present in patient samples was assessed by testing patient plasma in the capillary endothelial cell migration assay. Angiogenic activity followed over time was lowest in patients with the highest suramin concentrations and highest in patients with the lowest suramin concentrations. We conclude that it is feasible to continually monitor the activity of antiangiogenic agents in individual patients without relying on clinical tumor response. Copyright (C) 2000 S. Karger AG, Basel.

Original languageEnglish (US)
Pages (from-to)324-333
Number of pages10
JournalONCOLOGY
Volume58
Issue number4
DOIs
StatePublished - May 2000

Keywords

  • Antiangiogenesis
  • Breast cancer
  • Suramin

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

Fingerprint Dive into the research topics of 'A pilot trial of suramin in metastatic breast cancer to assess antiangiogenic activity in individual patients'. Together they form a unique fingerprint.

  • Cite this