Intraarterial infusion chemotherapy with lipioclol-CDDP suspension for hepatocellular carcinoma
- Osaka Medical College, Department of Radiology (Japan)
Purpose: To quantitatively evaluate the usefulness of lipiodol-CDDP suspension (LCS) chemotherapy in hepatocellular carcinoma (HCC).Methods: CDDP (cis-diamminedichloroplatinum) powder was prepared by removing the water and NaCl from aqueous CDDP. Two quantities of prepared CDDP powder, 10 mg and 20 mg, were mixed with 1 ml each of iopamidol 300 mgl/ml (IP300) and lipiodol (LPD) using a high pressure pumping method, thus producing LCS. Thirty-two patients with HCC, who had good renal function [creatinine clearance (Ccr) 50 ml/min or more], received additional intraarterial infusion chemotherapy with LCS or LCS alone.Results: The most frequently observed CDDP powder sizes were 5.95-10.90 {mu}m (average: 11.59 {mu}m). The LCS obtained demonstrated a suspension of 2-12 {mu}m (average 3.69 {mu}m) immediately after mixing, and no significant changes were observed in LCS particle sizes 3 hr after mixing. Moreover, the sustained release with LCS was observed for up to 3 hr. Meanwhile, the peripheral free platinum concentration between intraarterial infusion chemotherapy with LCS and intraarterial infusion with the aqueous solution of CDDP, with respect to variance residence time (VRT), showed a significant difference, with a p value of 0.0382. The survival rate was 89.84% at 1 year, 73.787c at 2 years, and 68.51% at 3 years. Furthermore, the platinum concentration in the tumor was 25-95 times the concentration in the surrounding liver parenchyma.Conclusion: Good clinical results can be expected by applying LCS to HCC.
- OSTI ID:
- 21414369
- Journal Information:
- Cardiovascular and Interventional Radiology, Vol. 23, Issue 1; Other Information: DOI: 10.1007/s002709910005; Copyright (c) 2000 Springer-Verlag; Article Copyright (c) 2000 Springer-Verlag New York, Inc; ISSN 0174-1551
- Country of Publication:
- United States
- Language:
- English
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CONTRAST MEDIA
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