Orally administered S-1 suppresses circulating endothelial cell counts in metastatic breast cancer patients

Int J Clin Oncol. 2014;19(3):452-9. doi: 10.1007/s10147-013-0570-5. Epub 2013 Jun 6.

Abstract

Background: S-1 is an oral cytotoxic preparation that contains tegafur. Gamma-butyrolactone (GBL) is a metabolite of tegafur that is known to suppress vascular endothelial growth factor (VEGF)-mediated angiogenic activity. The aim of this study was to determine the change in circulating endothelial cell (CEC) counts, GBL levels, and angiogenesis-related factors during S-1 administration in metastatic breast cancer (MBC) patients.

Methods: Patients with HER2-negative MBC were eligible. S-1 was administered orally twice daily in a 4 week on/2 week off cycle until disease progression or unacceptable toxicity occurred. Blood was collected on the following: days 1, 43, 85 (before each cycle of S-1 administration), days 15, 57 (1 h after S-1 administration), and day 29. The CellSearch(®) system was used to count the CECs. The gas chromatographic-mass spectrometric method was used to measure plasma GBL and 5-FU levels. Levels of VEGF were assayed by enzyme-linked immunosorbent assay.

Results: A total of 18 patients were enrolled. The plasma GBL levels on days 15 and 57 were 41.3 ± 15.8 and 41.0 ± 11.2 ng/mL, respectively. The CEC levels decreased on day 15, and significantly low levels were maintained until day 85 (P = 0.002 vs day 1). The plasma VEGF levels significantly decreased on day 15 (P = 0.012 vs day 1) and had a tendency to decrease until day 57.

Conclusions: This exploratory study showed that GBL levels increased, VEGF levels decreased, and CEC levels were suppressed during S-1 administration. S-1 appears to have anti-angiogenic activity.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Butyrolactone / blood
  • Administration, Oral
  • Adult
  • Aged
  • Antigens, CD34 / metabolism
  • Antimetabolites, Antineoplastic / administration & dosage
  • Antimetabolites, Antineoplastic / therapeutic use
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / pathology*
  • Cell Count
  • Chemokine CCL2 / blood
  • Drug Combinations
  • Endothelial Cells / drug effects*
  • Female
  • Fluorouracil / blood
  • Humans
  • Middle Aged
  • Neovascularization, Pathologic / drug therapy
  • Neovascularization, Pathologic / metabolism
  • Oxonic Acid / administration & dosage*
  • Oxonic Acid / therapeutic use*
  • Tegafur / administration & dosage*
  • Tegafur / therapeutic use*
  • Thrombospondin 1 / blood
  • Treatment Outcome
  • Vascular Endothelial Growth Factor A / blood

Substances

  • Antigens, CD34
  • Antimetabolites, Antineoplastic
  • CCL2 protein, human
  • Chemokine CCL2
  • Drug Combinations
  • Thrombospondin 1
  • VEGFA protein, human
  • Vascular Endothelial Growth Factor A
  • S 1 (combination)
  • Tegafur
  • Oxonic Acid
  • 4-Butyrolactone
  • Fluorouracil