Effects of Src kinase inhibition by saracatinib (AZD0530) on bone turnover in advanced malignancy in a Phase I study

Rosemary A Hannon1, Richard D Finkelman, Glen Clack

  • 1Academic Unit of Bone Metabolism, University of Sheffield, Sheffield, UK.

Bone
|January 17, 2012
PubMed

Insights

Saracatinib, a Src kinase inhibitor, significantly reduced bone resorption markers in patients with advanced cancer. This suggests potential therapeutic benefits for metastatic bone disease by inhibiting osteoclast activity.

Area of Science:

  • Oncology
  • Pharmacology
  • Bone Biology

Background:

  • Saracatinib (AZD0530) is an oral Src kinase inhibitor targeting cancer cell signaling pathways.
  • Advanced solid malignancies often present challenges with standard treatments and can involve bone complications.

Purpose of the Study:

  • To assess the impact of saracatinib on bone turnover in patients with advanced solid malignancies.
  • To evaluate the dose-dependent effect of saracatinib on bone resorption markers.

Main Methods:

  • Phase I study involving 51 patients with advanced solid malignancies.
  • Randomized administration of saracatinib at 50, 125, or 175 mg/day.
  • Measurement of serum (sCTX) and urinary (uNTX/Cr) bone turnover markers at multiple time points.

Main Results:

  • Saracatinib significantly decreased bone resorption markers in a dose-dependent manner.
  • Serum cross-linked C-terminal telopeptide of type I collagen (sCTX) decreased by -36% to -75% at day 28 across dosage groups.
  • Urinary cross-linked N-terminal telopeptide of type I collagen/creatinine ratio (uNTX/Cr) decreased by -13% to -50% at day 28 across dosage groups.

Conclusions:

  • Suppression of Src kinase by saracatinib inhibits osteoclast activity.
  • Saracatinib demonstrates potential therapeutic value in managing metastatic bone disease.
  • Further investigation into saracatinib for bone-related complications in cancer is warranted.

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