Detectable Inhibition of Heparin-Binding Growth Factor Activity in Sera From Patients Treated With Pentosan Polysulfate

• Published in: JNCI : Journal of the National Cancer Institute 1993-07, Vol.85 (13), p.1068-1073
• Main Authors: Parker, Bernard W., Swain, Sandra M., Zugmaier, Gerhard, DeLap, Robert L., Lippman, Marc E., Wellstein, Anton
• Format: Article
• Language: English
• Subjects: Antineoplastic agents; Biological and medical sciences; Biological Assay; Blood Coagulation - drug effects; Cell Division - drug effects; Chemotherapy; Growth Substances - blood; Humans; Medical research; Medical sciences; Neoplasms - blood; Neoplasms - drug therapy; Partial Thromboplastin Time; Pentosan Sulfuric Polyester - pharmacology; Pentosan Sulfuric Polyester - therapeutic use; Pharmacology. Drug treatments; Reference Values; Tumor Cells, Cultured; Tumors
• ISSN: 0027-8874; 1460-2105
• DOI: 10.1093/jnci/85.13.1068

Background: Previous studies indicate that the heparinoid pentosan polysulfate (PPS) can inhibit heparin-binding growth factors (HBGFs) released from tumor cells and thus block tumor growth in animal models. However, because of its heparin-like activity, the major toxic effect expected for PPS is its inhibition of coagulation. Purpose: Our purpose was to determine if anti-HBGF activity could be achieved in patients without causing complications from anticoagulation. Methods: We initiated a phase I trial in cancer patients and developed a cell proliferation assay to detect PPS in human serum based on its anti-growth factor activity. Blood samples from six healthy volunteers were collected in tubes containing different concentrations of PPS (FIBREZYM; concentration range, 0–10 μg/mL). Additional samples were obtained from four patients in the phase I trial before and after subcutaneous treatment with 15 mg/m2 of PPS. The activated partial thromboplastin time (aPTT), which is associated with coagulation, was measured in all blood samples. Serum prepared from the blood samples was heat inactivated and then incubated for 4–5 days with proliferating SW-13 cells, allowing determination of antigrowth factor activity. Results: PPS added to blood samples increased aPTT only at concentrations above 1 μg/mL, whereas HBGF-dependent proliferation was inhibited at less than 0.1 μg/mL. Sera obtained from patients up to 4 hours after PPS treatment specifically inhibited HBGF-dependent cell proliferation by more than 65% even at a 1:10 dilution. At the same time, the aPTT was not altered in these patients, indicating no significant effect on coagulation by this dose of the heparinoid. Conclusions: HBGF-inhibitory concentrations of PPS can be achieved in patients' sera without significant effects on coagulation. Implication: The assay presented here could be useful to determine doses and scheduling of treatment in studies evaluating PPS as an antitumor agent. [J Natl Cancer Inst 85:1068–1073, 1993]